Trabajos biology en Atlanta, GeorgiaCrear alertas

Full-time Dayshift and Nightshift Opportunities Available, PRN as well **Competitive Sign-On Bonus Available SOB AVAILABLE Independently performs laboratory procedures for which the technologist has been trained and demonstrated competency. Independently performs laboratory testing on patients of all ages using professional knowledge of laboratory procedures, executing, interpreting and/or analyzing, in an accurate and timely manner. Independently performs laboratory procedures for which the technologist has been trained and demonstrated competency. Independently performs laboratory testing on patients of all ages using professional knowledge of laboratory procedures, executing, interpreting and/or analyzing, in an accurate and timely manner. Education • H.S. Diploma or General Education Degree (GED) plus a sufficient number of college and/or technical school courses and clinical training to satisfy the requirements for testing and certification as a medical technologist by an approved certifying agency Required, • Bachelor's Degree in clinical laboratory science, biomedical science, medical technology or in a life / biological science (biology, biochemistry, microbiology, etc.) Preferred, • No experience required Required, • 1 year of supervised clinical experience as a medical technologist in a clinical laboratory Preferred, • Certification as a medical technologist or medical laboratory scientist by the American Society of Clinical Pathologists (ASCP), AMT (American Medical Technologists) or AAB (American Association of Bioanalysts) according to the qualifications through the State of Georgia Department of Community Health, Healthcare Facility, Clinical Laboratory regulations. Upon Hire Required or, • A person who recently moved into the state of Georgia or recently completed the academic and training/experience requirements may be temporarily classified as technologists or technicians for eighteen (18) months only to afford the person an opportunity to successfully complete an approved qualifying examination. within 1-1/2 Yrs Required, • AAB provisional certification not accepted Piedmont Atlanta Hospital

Independently performs laboratory procedures for which the technologist has been trained and demonstrated competency. Independently performs laboratory testing on patients of all ages using professional knowledge of laboratory procedures, executing, interpreting and/or analyzing, in an accurate and timely manner. Independently performs laboratory procedures for which the technologist has been trained and demonstrated competency. Independently performs laboratory testing on patients of all ages using professional knowledge of laboratory procedures, executing, interpreting and/or analyzing, in an accurate and timely manner. • H.S. Diploma or General Education Degree (GED) plus a sufficient number of college and/or technical school courses and clinical training to satisfy the requirements for testing and certification as a medical technologist by an approved certifying agency Required, • Bachelor's Degree in clinical laboratory science, biomedical science, medical technology or in a life / biological science (biology, biochemistry, microbiology, etc.) Preferred, • No experience required Required, • 1 year of supervised clinical experience as a medical technologist in a clinical laboratory Preferred, • Certification as a medical technologist or medical laboratory scientist by the American Society of Clinical Pathologists (ASCP), AMT (American Medical Technologists) or AAB (American Association of Bioanalysts) according to the qualifications through the State of Georgia Department of Community Health, Healthcare Facility, Clinical Laboratory regulations. Upon Hire Required or, • A person who recently moved into the state of Georgia or recently completed the academic and training/experience requirements may be temporarily classified as technologists or technicians for eighteen (18) months only to afford the person an opportunity to successfully complete an approved qualifying examination. within 1-1/2 Yrs Required, • AAB provisional certification not accepted Piedmont Atlanta Hospital

Computational Biologist I – Biological Imaging & Database Development Atlanta, GA (Onsite), United States (On-site) Position Summary: Computational Biologist I provides specialized computational biology, database development, and analytical support to CDC research programs. This position is responsible for designing, developing, and maintaining a centralized database to store, organize, retrieve, and visualize biological images and experimental data generated through high-content imaging and high-through put screening activities. Compensation & Benefits: Starting Salary Range for Computational Biologist I – Biological Imaging & Database Development: $95,000.00-105,000.00/yr Benefits That Set Us Apart When considering your next opportunity, compensation is only part of the picture. We offer a benefits package designed to invest in your future and support your life outside of work. Highlights include: • Up to a 6% 401(k) company match to help you build long-term financial security, • Paid time off as part of our comprehensive benefits package, so you have the flexibility to rest, recharge, and enjoy what matters most, • Medical, dental, and vision insurance, plus prescription drug coverage, • Basic life and AD&D insurance, with supplemental life options, • Short-term and long-term disability coverage, • Paid holidays, • Employee Assistance Program (EAP), • Flexible Spending Account (FSA) and Health Savings Account (HSA) options, • Professional development, training, and certification support, • Voluntary benefits including accident, critical illness, and identity theft protection Because taking care of our employees isn’t just a promise, it’s part of who we are. Benefits are subject to change and eligibility requirements apply. Essential Functions, Duties & Responsibilities: Includes the following: • Design, develop, and maintain a centralized database for biological images, experimental metadata, and high-throughput screening results., • Develop scalable database architectures, data models, and automated workflows for image storage, integration, and retrieval., • Create advanced search, indexing, and customizable filtering capabilities to support efficient exploration of biological datasets., • Develop interactive dashboards and visualization tools that allow researchers to view, compare, and analyze biological images and associated experimental results., • Integrate imaging data with experimental metadata, cellular measurements, assay results, and other scientific information., • Develop and maintain computational applications and automated processes using Python, SQL, R, or comparable programming languages., • Implement data validation, quality control, and database optimization processes to ensure accuracy, integrity, and performance., • Support computational image analysis, feature extraction, and statistical evaluation of biological imaging data., • Collaborate with laboratory scientists and technical teams to define requirements, enhance database functionality, and support scientific research., • Prepare technical documentation and provide ongoing troubleshooting and system support., • Perform other duties as assigned., • Computational Biologist I Experience, Education, Skills, Abilities requested:, • Design, develop, and maintain a centralized database for biological images, experimental metadata, and high-throughput screening results., • Develop scalable database architectures, data models, and automated workflows for image storage, integration, and retrieval., • Create advanced search, indexing, and customizable filtering capabilities to support efficient exploration of biological datasets., • Develop interactive dashboards and visualization tools that allow researchers to view, compare, and analyze biological images and associated experimental results., • Integrate imaging data with experimental metadata, cellular measurements, assay results, and other scientific information., • Develop and maintain computational applications and automated processes using Python, SQL, R, or comparable programming languages., • Implement data validation, quality control, and database optimization processes to ensure accuracy, integrity, and performance., • Support computational image analysis, feature extraction, and statistical evaluation of biological imaging data., • Collaborate with laboratory scientists and technical teams to define requirements, enhance database functionality, and support scientific research., • Prepare technical documentation and provide ongoing troubleshooting and system support., • Perform other job-related duties as assigned. Supervisory Responsibilities: No supervisory/management authority Basic Qualifications: • Prolonged periods of sitting at a desk and working on a computer; may occasionally require standing or moving about the office for extended periods., • Must pass pre-employment qualifications of Cherokee Federal. Preferred Qualifications: • Master’s degree in Computational Biology, Bioinformatics, Computer Science, Biomedical Informatics or related field preferred., • Experience developing scientific imaging databases or biological image repositories., • Experience applying advanced analytics, machine learning, artificial intelligence, predictive modeling, or computational methods to public health data. Work Environment: Work is performed primarily in a climate-controlled environment. Company Information: Behind every government mission stands skilled, mission-driven talent: people whose expertise and dedication turn complex challenges into successful outcomes. Cherokee Nation Integrated Health, part of Cherokee Federal, the federal contracting division of Cherokee Nation Businesses, is that team. We modernize aging systems, deliver care where it’s needed most, and keep missions supplied, staffed, and moving across defense, intelligence, and civilian agencies. For more than 60 federal clients, we take on the work others won’t, and deliver where it counts. If that’s the kind of work you’re looking for, you’ve found your team. Learn more at cherokee-federal.com. #CherokeeFederal #LI-RN1 Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply. Legal Disclaimer: All qualified applicants will receive consideration for employment without regard to protected veteran status, disability or any other status protected under applicable federal, state or local law. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Equal Employment Opportunity (EEO) Statement Cherokee Federal is a federal contractor subject to the Vietnam Era Veterans’ Readjustment Assistance Act (VEVRAA). As required by VEVRAA, we take affirmative action to employ and advance in employment qualified protected veterans. Protected veterans are encouraged to self-identify during the application process. Cherokee Federal takes affirmative action to employ and advance in employment qualified individuals with disabilities in compliance with Section 503 of the Rehabilitation Act. Qualified individuals with disabilities are encouraged to self-identify during the application process. Reasonable accommodations are available to qualified individuals with disabilities or those with sincerely held religious beliefs. To request an accommodation in the application or interview process, please contact Human Resources at careers@cherokee-federal.com.

Job Description Great Hill Solutions, LLC is part of the Seneca Nation Group (SNG) portfolio of companies. SNG is Seneca Holdings' federal government contracting business that meets mission-critical needs of federal civilian, defense, and intelligence community customers. Our portfolio comprises multiple subsidiaries that participate in the Small Business Administration 8(a) program. To learn more about SNG, visit the website and follow us on LinkedIn. Our team of talented individuals is what makes us successful. To support our team, we provide a balanced mix of benefits and programs. Your total rewards package includes competitive pay, benefits, and perks, flexible work-life balance, professional development opportunities, and performance and recognition programs. We offer a comprehensive benefits package that includes medical, dental, vision, life, and disability, voluntary benefit programs (critical illness, hospital, and accident), health savings and flexible spending accounts, and retirement 401K plan. One of our fundamental principles is to offer competitive health and welfare benefits to our team members, providing coverage and care for you and your family. Full-time employees working at least 30 hours a week on a regular basis are eligible to participate in our benefits and paid leave programs. We pride ourselves on our collaborative work environment and culture, which embraces our mission of providing financial and non-financial benefits back to the members of the Seneca Nation. Great Hill is seeking a Quality Assurance Specialist to join our team in Atlanta, GA. The Quality Assurance Specialist provides comprehensive laboratory quality assurance, quality management system (QMS), and safety program support for the Centers for Disease Control and Prevention's (CDC) Coronavirus and Other Respiratory Viruses Division (CORVD). This role supports laboratory quality initiatives by ensuring compliance with federal regulations, laboratory accreditation requirements, quality standards, biosafety requirements, and CDC policies. The QA specialist assists with audit readiness, corrective action management, quality improvement initiatives, safety compliance monitoring, equipment management, risk assessments, and Quality Management System implementation across laboratory operations. The position serves as a key liaison between laboratory personnel, quality management staff, safety officers, and leadership to promote continuous quality improvement, operational excellence, and regulatory compliance. MAJOR DUTIES AND RESPONSIBILITIES • Support implementation, maintenance, and continuous improvement of Laboratory Quality Management Systems (QMS) to ensure compliance with CDC, CMS, CLIA, and applicable regulatory requirements., • Conduct quality assessments, gap analyses, compliance reviews, and corrective action follow-up activities to identify and resolve quality management issues., • Review, document, and monitor Non-Conforming Events (NCEs), deviations, corrective actions, preventive actions, and quality performance metrics., • Coordinate laboratory audit readiness activities, including inspection preparation, compliance assessments, documentation reviews, and regulatory support., • Manage laboratory temperature monitoring and environmental control programs, including review of alarm notifications, temperature excursions, trend analyses, and corrective actions., • Maintain equipment inventories and support calibration, preventive maintenance, qualification, and replacement planning activities for laboratory systems and instrumentation., • Support laboratory safety programs through safety compliance monitoring, training record management, hazard assessments, biosafety reviews, and incident investigations., • Develop, revise, and maintain quality and safety Standard Operating Procedures (SOPs), policies, work instructions, and controlled documentation., • Provide quality and safety training support, communicate quality initiatives to laboratory personnel, and participate in laboratory improvement and compliance working groups., • Conduct risk assessments, identify quality and safety risks, recommend mitigation strategies, and support implementation of continuous quality improvement initiatives. QUALIFICATIONS Education and Experience: • Bachelor's degree in Medical Laboratory Science, Biology, Microbiology, Chemistry, Biochemistry, Life Sciences, or a related scientific field., • Master's degree preferred., • Certification as a Medical Technologist (MT), Medical Laboratory Scientist (MLS), Clinical Laboratory Scientist (CLS), or equivalent certification from an accredited professional certification board (e.g., ASCP, AMT, or AAB) is preferred., • Experience working within CLIA, CMS, CAP, or ISO-regulated laboratory environments is highly desirable. CORE COMPETENCIES (Required Skills): • Quality Management Systems (QMS), • CAPA Management, • Risk Assessment & Mitigation, • Audit & Inspection Readiness, • CMS/CLIA Compliance, • Biosafety & Laboratory Safety Programs, • Equipment Lifecycle Management, • Temperature Monitoring Systems (e.g., MESA), • SOP Development & Document Control, • Quality Metrics & Reporting, • Regulatory Compliance Management, • Must be a United States citizen or permanent resident or have authorization for employment in the United States to obtain and maintain the necessary security clearance for this role. Equal Opportunity Statement: Seneca Holdings provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex/gender, sexual orientation, national origin, age, disability, marital status, genetic information and/or predisposing genetic characteristics, victim of domestic violence status, veteran status, or other protected class status. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation and training. The Company also prohibits retaliation against any employee who exercises his or her rights under applicable anti-discrimination laws. Notwithstanding the foregoing, the Company does give hiring preference to Seneca or Native individuals. Veterans with expertise in these areas are highly encouraged to apply.

Job Description The Atlanta VA Medical Center (VAMC) Research Service seeks an outstanding investigator with expertise in advanced artificial intelligence methods to support and advance VA research focused on cancer detection, prognosis, treatment selection, and survivorship. The investigator will work in a multidisciplinary VA research environment and collaborate with computational scientists, oncologists, radiologists, pathologists, and other clinical and research professionals. This position offers an exceptional opportunity to generate and translate practice-changing evidence on the responsible use of AI in oncology within the Veterans Health Administration (VHA), the nation's largest integrated health system. The work will focus on improving outcomes, reducing disparities, and enhancing patient safety for Veterans, including those affected by tobacco-, environmental-, and service-related cancer risks. About the Opportunity The successful candidate will lead or co-lead collaborative, innovative research applying AI to Veteran cancer care. Potential areas of research include: -Radiopathomics: computational fusion of CT/MRI radiomics with digital pathology (H&E whole-slide) features to predict prognosis and treatment response in non-small cell and small cell lung cancer, prostate cancer, and other Veteran-prevalent malignancies. -Computational pathology of the tumor microenvironment, including tumor-infiltrating lymphocyte architecture, vascular and stromal/collagen organization, and immune-cell spatial patterning, as prognostic and predictive biomarkers. -Radiogenomics and multimodal data integration (clinical, imaging, pathology, and molecular/genomic) to improve cancer phenotyping, risk stratification, and prediction of response to immunotherapy and chemotherapy. -AI-driven imaging biomarker development leveraging national data infrastructure such as the Medical Imaging and Data Resource Center (MIDRC), with an eye toward validation in VA's Corporate Data Warehouse (CDW), VA Science and Data Platform (SDP), and the Million Veteran Program (MVP). -Emerging approaches involving agentic AI and foundation models for contextualized, multimodal cancer decision support and the development of interpretable clinical AI tools. AI for cancer research and care delivery is a strategic priority for the Atlanta VAMC and the VA Office of Research and Development nationally, with growing emphasis on responsible, real-world implementation across the VA health care system. This work is well suited for external funding from federal agencies and other research sponsors, and the successful candidate will be positioned to translate advanced AI methods into pragmatic, implementation-focused research that benefits Veterans nationwide. VA Research Environment This role is embedded within the Atlanta VAMC Research Service and supports a broad portfolio of collaborative research addressing high-priority health concerns affecting Veterans. The research environment brings together investigators, clinicians, data scientists, and research staff with expertise in cancer, medical imaging, digital pathology, precision medicine, and health care delivery. The successful candidate will benefit from access to VA research resources, relevant clinical and imaging data, established computational capabilities, and close collaboration with VA clinical and research leadership. Opportunities may also include participation in multidisciplinary clinical conferences, national VA research collaborations, and projects using VA data platforms and other approved research infrastructure. Strategic Impact This recruitment will strengthen the Atlanta VA's capacity for AI-enabled precision oncology research and implementation science. The position will help advance the development and evaluation of radiopathomic and multimodal AI approaches for Veteran cancer screening, diagnosis, prognosis, and treatment; support the responsible integration of research findings into VA care; and contribute to equitable, evidence-based cancer care for Veterans, including those affected by service-related and environmental exposures. Key Responsibilities Develop and sustain an independent or co-led, externally funded research program in AI and precision oncology within VA; collaborate with VA investigators, clinicians, data scientists, and research staff on high-priority Veteran health questions; contribute to multidisciplinary and multi-site studies across the national VA research network; mentor trainees and junior investigators; and disseminate findings through peer-reviewed publications, national presentations, and competitive grant applications. Qualifications PhD with postdoctoral training, or MD/MD-PhD with relevant research training, in biomedical engineering, computer science, computational biology, biomedical informatics, or a related quantitative field. Candidates should demonstrate expertise in one or more of the following: computer vision and deep learning for radiology or digital pathology images; radiomics, pathomics, or radiogenomics; multimodal data fusion; or large language model/agentic AI applications in oncology. Experience securing or competing for external research funding (e.g., NIH/NCI, VA Merit Review), a strong record of peer-reviewed publications, and the ability to work effectively in a multidisciplinary, clinician-integrated VA research environment are expected. Eligibility for a VA research appointment (including any required background processes) is required; rank and appointment level (e.g., Research Health Scientist, Research Career Scientist track) will be commensurate with qualifications and experience. Commitment to Inclusion The Atlanta VA Medical Center is committed to equity, inclusion, and diversity in research and care. Veterans, women, and applicants from groups underrepresented in medicine and science are strongly encouraged to apply. Application Process Interested candidates should submit a curriculum vitae (CV) and a cover letter (maximum 2 pages) describing research interests, career goals, and relevance to AI in precision oncology and VA cancer care. Location: Atlanta VA Medical Center, Decatur, Georgia The U.S. Department of Veterans Affairs is an Equal Opportunity Employer.

Job Description The Environmental Field Technician (Technician) will be responsible for the collection of waste chemicals and Universal Wastes from the CDC laboratories and workplaces and transport them containers to the appropriate storage areas. The Technician will become familiar with chemical segregation such that they will assist the Project Manager (PM) with placing chemical wastes into temporary storage for offsite shipment. The Technician will assist the Project Manager in the entry and compilation of waste generation tracking data into the client's proprietary data base. The Technician's understanding of applicable environmental regulations such that they will perform compliance inspections of waste accumulation areas and provide follow-up reports to the PM. The Technician will be trained to be knowledgeable of available spill clean-up materials/procedures and assist the PM with the clean-up in the event that a spill occurs while waste is being transported to the waste storage areas. The Technician will perform an inspection of the clients Spill Control Centers (SCC) in compliance with the client Project Work Scope. SCC inspection reports will be provided to the PM monthly. Using materials provided by the Client, the Technician will be responsible of restocking any SCC with required supplies on as needed basis. The Technician will support the client's sustainability program by collecting for recyclable materials generated by CSS chemical waste management activities. These materials include but are not limited to empty plastic and glass containers. Candidates must have an Associate's degree (Bachelor's preferred) in a scientific discipline that qualifies them to evaluate hazards associated with chemicals and chemical wastes. Examples include: Chemistry, Chemical Technology, Biology, Environmental Science, etc. Qualified individual must be able to read, write, and speak English fluently. Candidates may not have a criminal record. They must be able to pass a background check, allowing them to obtain an HHS/CDC site badge. Individual must have a valid driver's license. This is a temporary postion, with the opportunity to transtion to permanent employment. PREFERRED SKILLS/KNOWLEDGE Good knowledge and understanding of all federal, state, and local laws and regulations pertaining to the Environmental Services Industry including experience with RCRA and DOT regulations. Introductory knowledge of high hazard materials management/assessment and cylinder handling. Must have 40-hour OSHA HAZWOPER certification with recurrent training. Must be in good physical condition in order to regularly lift 50 pound containers, load trucks during chemical and hazardous waste shipments, handle 55 gallon drums and them using a drum cart, and respond to chemical spills as necessary.Excellent internal skill necessary to effectively communicate with the Project Manager and client personnel. Working knowledge or Microsoft Office suite software. CSS is an Equal Opportunity/Affirmative Action Employer who provides equal employment opportunities to all employees and applicants for employment without regards to race, color, religion, sex, gender identity, sexual orientation, pregnancy, national origin, age, disability, veteran status or genetic information. In addition to federal law requirements, CSS complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Job Description ABOUT OUR SCHOOL Atlanta International School (AIS) is a 3K to Grade 12 IB World School that brings together students, educators, and families from more than ninety countries. Guided by our three pillars of the IB Continuum, Intercultural Understanding, and Language Learning, AIS offers a globally minded, inquiry-driven education that prepares students to lead with purpose and integrity. Our Buckhead Campus is an urban learning environment in the heart of Atlanta, giving students access to the cultural, academic, and professional opportunities of a major international city. Museums, universities, arts institutions, and civic organizations serve as extensions of our classrooms. Our Sandy Springs Campus sits on twenty four wooded acres along the Chattahoochee River and is home to the Mouratoglou Atlanta Academy tennis program. This nature-rich setting provides space for outdoor learning, partnerships, and unique student experiences. Across both campuses, AIS delivers a unified curriculum through the full IB continuum. Students pursue multiple pathways to graduation, including the IB Diploma Programme, the IB Careers-related Programme, AISx flexible pathways, and the AIS Impact Diploma. Within our diverse and multilingual community, students grow as critical thinkers, collaborators, and compassionate leaders who make a meaningful impact in the world. Our School is committed to the safety and well-being of every child. We maintain rigorous safeguarding practices to ensure a secure, supportive, and nurturing environment where all students can thrive. JOB PURPOSE The Science Lab Manager oversees the operational, technical, and safety systems of the Secondary School Science laboratories. This role ensures that laboratory spaces, equipment, materials, and procedures effectively support inquiry-based learning aligned with the IB Middle Years Programme (MYP) and Diploma Programme (DP). The Science Lab Manager coordinates laboratory operations across Biology, Chemistry, Physics, and interdisciplinary science learning spaces while supporting student research, departmental logistics, safety compliance, inventory systems, and laboratory readiness. This role collaborates closely with Science teachers, Subject Leaders, IB Coordinators, operational teams, and school leadership to maintain safe, organized, and responsive laboratory environments that support high quality teaching and learning. This is a part-time position within the Secondary School Science Department. FLSA: Exempt Reports to: Science Lab Manager Secondary Accountability: Science Group Leader AIS CORE VALUES BASED COMPETENCIES • Commitment to Growth – Seeks continuous self-improvement., • Collaborative Teamwork – Builds strong, supportive relationships., • Adaptability – Maintains flexibility and openness to change., • Inclusivity – Actively welcomes and engages diverse perspectives., • Empathy – Shows compassion and understanding toward others., • Intercultural Communication – Communicates effectively across cultures., • Bias Awareness – Recognizes and mitigates personal biases., • Task Prioritization – Manages time and tasks efficiently., • Accountability – Takes responsibility for actions and outcomes., • Constructive Conflict Resolution – Resolves conflicts in a restorative way. RESPONSIBILITIES As the Science Lab Assistant, you will contribute to a safe, organized, and inquiry-driven learning environment that supports practical science learning across Grades 6 to 12 with a focus in the MYP program. Strong organizational skills, attention to detail, and a collaborative mindset are essential. 1. Provide Classroom Logistics & Operational Support • Serve as a primary responder for immediate classroom resource needs and laboratory support requests., • Support teachers in maintaining organized, functional, and well-stocked laboratory and classroom spaces., • Regularly audit and restock classroom and laboratory supplies, including safety equipment and commonly used materials., • Monitor laboratory readiness and communicate resource or maintenance needs to the Science Lab Manager. 2. Support Laboratory Preparation & Breakdown, • Prepare equipment, materials, and chemical reagents for laboratory activities as directed by the Science Lab Manager and science faculty., • Support laboratory setup, breakdown, and cleanup processes., • Ensure equipment is cleaned, maintained, and returned to appropriate storage locations following use., • Assist with the movement and distribution of laboratory materials between preparation spaces and classrooms. 3. Maintain Equipment & Resources, • Perform routine maintenance and minor repairs on laboratory equipment., • Clean, sterilize, and maintain laboratory equipment and glassware according to established procedures., • Assist the Science Lab Manager with specialized laboratory preparations and technical tasks., • Support inventory tracking and organization of laboratory materials and equipment. 4. Support Health, Safety & Compliance, • Assist in maintaining laboratory safety standards and procedures., • Ensure Safety Data Sheets (SDS) and other required safety documentation are available and accessible., • Support safe storage, handling, and disposal procedures for laboratory materials., • Respond to laboratory incidents and concerns in accordance with established school safety protocols., • Assist with annual inventory audits of chemicals and laboratory equipment. 5. Support Teaching & Learning, • Assist teachers during laboratory activities when requested., • Support student safety and proper equipment use during practical learning experiences., • Assist with science fairs, research projects, exhibitions, and other departmental initiatives as assigned., • Contribute to the smooth operation of inquiry-based science learning experiences. 6. Engage in Professional Learning & Collaboration, • Attend department meetings and required school professional learning activities., • Collaborate positively with faculty, staff, and operational teams., • Maintain professionalism, confidentiality, and a commitment to student safety and wellbeing., • Support the mission, vision, and values of Atlanta International School. JOB

Job Description Job Title: Quality Technician Location: Forest Park, GA Type: Contract To Hire Compensation: $22.00/hr Work Model: Onsite – onsite Hours: 6 PM to 6 AM Responsibilities • Perform wet chemical analyses, • Prepare and standardize lab stock reagents as needed, • Order, receive, stock and maintain inventory of chemicals, reagents and consumable supplies, • Interpret MSDS information with respect to lab chemicals and finished products, • Identify tests to perform based on product testing matrices, • Record data in computer and/or logbooks and compose SPC charts for data analysis, • Use of SAP to retrieve product specifications and test limits, • Maintain and troubleshoot laboratory equipment to include scales, pH meters, viscometers, and autotitrators, • Maintain housekeeping in the department as required, • Support project work as necessary, • Demonstrate the proper use of lab-ware including volumetric and non-volumetric, including menisci reading for graduated cylinder/burette/volumetric flasks, • Conduct Finish Case Inspections and other Quality checks on Packaging Lines, • Prepare and maintain Target/Reject bottles, • Support WCM processes including Early Management, Daily Operations and other Pillars Requirements • Associate's or Bachelor's degree in Chemistry, Biology, Chemical Engineering, or a related scientific discipline, or equivalent laboratory experience, • Minimum 1-3 years of experience in a laboratory, quality control, manufacturing, or chemical testing environment, • Demonstrated knowledge of wet chemistry techniques, reagent preparation and standardization, laboratory safety practices, and chemical handling procedures, • Ability to interpret Safety Data Sheets (SDS/MSDS), follow testing protocols and product testing matrices, and comply with applicable safety and quality standards, • Experience operating, calibrating, maintaining, and troubleshooting laboratory equipment including pH meters, analytical balances, viscometers, autotitrators, and related instrumentation, • Proficiency with computer-based data entry, statistical process control (SPC) charting, laboratory documentation, and enterprise systems such as SAP, • Strong understanding of laboratory glassware and measurement techniques, including accurate use of volumetric and non-volumetric equipment and proper meniscus reading, • Experience managing laboratory inventory, ordering chemicals and supplies, and maintaining organized stock and storage areas, • Ability to perform quality inspections, packaging line quality checks, finish case inspections, and maintain product standards through target/reject sample management, • Experience in consumer products, food & beverage, pharmaceutical, chemical manufacturing, or similar regulated industries, • Familiarity with Good Manufacturing Practices (GMP), ISO quality systems, Lean Manufacturing, or World Class Manufacturing (WCM) methodologies, • Certification or training in laboratory safety, hazardous materials handling, statistical quality control, or quality assurance processes System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #558-Scientific

Job Description An Environmental Laboratory Analyst is responsible for testing environmental samples to determine the presence of pollutants and other contaminants. They analyze samples using specialized equipment and techniques, playing a critical role in ensuring compliance with federal, state, and local environmental regulations. Key Responsibilities • Sample Analysis: Analyze various types of samples, including process water, coal, fuel oil, and compliance water samples. • Environmental Documentation: Maintain accurate records, permits, and documentation required for environmental compliance and reporting. Qualifications • Education: Bachelor’s degree in Chemistry, Biology, Microbiology, or Environmental Sciences. • Experience: Several years of experience performing laboratory analysis; familiarity with EPA methods or environmental testing is a plus. • Technical Skills: Proficiency with laboratory testing equipment and adherence to safe laboratory practices. • Communication: Strong written and verbal communication skills to effectively convey technical information and compliance requirements. • Problem-Solving: Excellent problem-solving skills to address complex issues and recommend innovative solutions. • Attention to Detail: High level of accuracy in documenting environmental data and ensuring regulatory compliance. • Teamwork: Ability to work collaboratively with colleagues, stakeholders, and multidisciplinary teams to achieve environmental objectives. • Analytical Skills: Strong analytical thinking to interpret environmental data, identify trends, and provide actionable recommendations.

Job DescriptionBS degree in Chemistry or related science field (ie Biology) Experience working in a laboratory performing • Chemical analysis including, but not limited to TSS, Oil & Grease,, • Ion chromatography,, • Gas chromatography,, • ICP-MS,, • atomic absorption,, • coal and/or fuel oil sulfur content. Handling, preparing, and analyzing various environmental samples according to EPA, ASTM, or other protocols. Experience with quality control requirements for analytical methods. Experience in chemical nomenclature, instrumentation, and inorganic analytical methods including EPA methodology supporting NPDES, RCRA, CERCLA, TSCA, and EPA Solid Waste - 846 methods (Test Methods for Evaluating Solid Waste, Physical/Chemical Methods).

Job Description Title: Quality Assurance Analyst Compensation: $60-72k Location: College Park, Georgia Benefits: Medical, Dental, Vision, FSA/HSA About the Company: Nitro is a Brazilian multinational that marked 90 years in business in 2025, tracing its roots back to its founding in 1935. The company is recognized as a pioneer in Brazil's modern chemical industry and is one of the country's largest suppliers of nitrocellulose. Nitro serves clients in more than 70 countries and operates in Brazil, Uruguay, the United States, and Europe. Since 2019, the company has expanded into agribusiness specialty products through the acquisition of several units, broadening its portfolio to serve all of Brazil. In recent years, Nitro has seen strong growth, with revenue increasing more than 30% annually and sales growth exceeding 40%, supported by a workforce of over 1,200 employees. In the U.S., Nitro operates as Nitro Quimica Corporation, located at 2300 West Point Avenue in the Atlanta, Georgia area (College Park), where the company supports its North American operations and customer base. Job Summary: The Quality Assurance Analyst plays a critical role in supporting Nitro's quality management system across the Quality Control Laboratory and broader manufacturing operations. This position is responsible for reviewing and approving analytical and batch documentation, verifying compliance with established procedures and specifications, and driving continuous improvement in quality processes—particularly for pharmaceutical raw materials, in-process materials, and finished products. The role also owns document control and training records within MasterControl, and supports FDA and ISO 9001 compliance through internal and external quality audits. As a key member of the Quality team, this role works cross-functionally with the laboratory, production, and customer-facing teams to ensure every batch and shipment meets Nitro's quality standards prior to release. Job Duties and Responsibilities: Quality Review & Release • Review and approve contract and internal laboratory results for raw materials and finished products., • Review testing status and approve pharmaceutical raw materials prior to use in production., • Review and approve labeled raw material containers and finished product drums prior to shipment., • Confirm and sign off on pharmaceutical production batches, verifying compliance with specifications. Documentation & Batch Records • Prepare and maintain pharmaceutical batch documentation for use in manufacturing., • Review, verify, and file completed pharmaceutical batch documentation for accuracy and completeness., • Maintain accurate records of testing, retesting, and approval status for incoming raw materials. Document Control & Training • Own document control processes within MasterControl, including creation, revision, routing, and approval of SOPs, specifications, and quality records., • Maintain and audit employee training records to ensure completion and compliance with current procedures., • Coordinate training assignments in MasterControl when documents are created or revised, and track completion status., • Ensure documentation practices meet FDA requirements for OTC pharmaceutical manufacturing and ISO 9001 record-keeping standards. Regulatory Compliance & Audits • Support compliance with FDA regulations applicable to OTC pharmaceutical manufacturing (21 CFR 210/211) and the site's ISO 9001 quality management system., • Plan, lead, and conduct internal quality audits; support external and regulatory audits and inspections., • Identify audit findings and nonconformances, and track corrective and preventive actions (CAPA) to closure., • Support maintenance and continuous improvement of the quality management system to sustain FDA and ISO 9001 compliance. Laboratory & Quality Systems Oversight • Oversee and coordinate analytical and physical testing performed in support of production batches (lacquer, acid, and topical pharmaceutical batches), including methods such as gas chromatography and HPLC., • Coordinate sampling of pharmaceutical raw materials upon receipt., • Manage submission and tracking of active pharmaceutical ingredient (API) testing., • Monitor and maintain calibration schedules for laboratory instrumentation (gas chromatographs, HPLC, balances, standard thermometers, etc.), including Operational Qualification and Preventative Maintenance due dates., • Perform and document instrument calibrations according to the analytical plan. Cross-Functional & Customer Support • Prepare developmental samples for customer evaluation., • Package finished product and developmental samples for shipping., • Serve as a technical resource for contract laboratories, customers, and internal personnel on quality-related questions., • Support laboratory organization, consumable inventory, and overall lab readiness. Requirements: • Bachelor's degree in Chemistry or a related science (Biology, Biochemistry, Chemical Engineering) required., • Minimum of 6 months of experience in an analytical laboratory or quality environment., • Working knowledge of FDA regulations as applied to OTC pharmaceutical manufacturing (21 CFR 210/211) required., • Working knowledge of ISO 9001 quality management system requirements required., • Experience with document control and training record management, preferably within MasterControl or a similar electronic quality management system., • Internal or external quality audit experience required; Lead Auditor certification (e.g., ISO 9001 Lead Auditor) strongly preferred., • Working knowledge of analytical and organic testing methods and laboratory safety practices., • Fluent in English., • Strong verbal and written communication skills., • Critical thinking and investigative skills., • Highly organized with strong attention to detail., • Demonstrated ability to work effectively as part of a team. This search is being conducted by Flex HR on behalf of Nitro. Qualified candidates should submit a resume within. Flex HR uses AI for document preparation and meeting transcription only — never to screen or evaluate candidates. All hiring decisions are made by a human recruiter. Roles may be posted on platforms like Indeed or LinkedIn, which are independent companies that may use AI in their own technology.

Job Description Job title: Environmental Laboratory Analyst 1 Duration: 12+ Months Location: Atlanta, GA, US Pay range: $20-$23/hr on W2 Job description An Environmental Laboratory Analyst is responsible for gathering, monitoring and testing of environmental samples to determine the presence of pollutants and other contaminants. They collect samples from various sources, such as air, water, and soil, analyze them using specialized equipment and techniques. They play a critical role in ensuring compliance with federal, state, and local environmental regulations. Key Responsibilities: System Monitoring: Monitor environmental systems, such as wastewater treatment, air pollution control, and waste management. Environmental Compliance: Monitor and ensure compliance with local, state, and federal environmental regulations, permits, and standards relevant to the organization's operations. Data Analysis: Collect and analyze environmental data, including air and water quality data, to assess environmental conditions, trends, and system performance. Emergency Response: Knowledge of emergency response plans for environmental incidents, spills, and accidents. Environmental Documentation: Maintain accurate records, permits, and documentation required for environmental compliance and reporting. Qualifications: Education: Bachelor’s degree in Chemistry, Biology, Microbiology, Environmental Sciences or Associate’s degree in Chemistry, Biology, Microbiology, or Environmental Sciences Experience: Several years of experience in environmental monitoring and testing, with a strong understanding of environmental regulations and industrial processes. Environmental Regulations: Profound knowledge of local, state, and federal environmental regulations, permits, and standards. Technical Skills: Proficiency in environmental monitoring equipment, data analysis tools, and environmental modeling software. Communication: Effective communication skills, both written and verbal, to convey technical information and compliance requirements. Problem-Solving: Strong problem-solving abilities to address complex environmental challenges and recommend innovative solutions. Attention to Detail: Meticulous attention to detail to ensure accuracy in environmental documentation and regulatory compliance. Teamwork: Ability to collaborate effectively with colleagues, stakeholders, and multidisciplinary teams to achieve environmental goals. Analytical Skills: Strong analytical thinking to assess environmental data, identify trends, and make informed recommendations. \nCompany Description LanceSoft is a global workforce solutions and IT services firm founded in 2000, specializing in temporary/permanent staffing, IT services, and outsourcing (RPO) for sectors like healthcare and IT. Headquartered in Herndon, Virginia, with a significant presence in India, the certified minority/woman-owned company employs over 5,700 professionals LanceSoft is a global workforce solutions and IT services firm founded in 2000, specializing in temporary/permanent staffing, IT services, and outsourcing (RPO) for sectors like healthcare and IT. Headquartered in Herndon, Virginia, with a significant presence in India, the certified minority/woman-owned company employs over 5,700 professionals

Job Description SUMMARY OF FUNCTIONS: The Nature Curriculum Coordinator will be responsible for the implementation of the Frazer Nature Curriculum for Frazer Center Childcare and Pre-K students, as well as community outreach and engagement with other Early Childhood Education programs in the metro Atlanta area, in coordination with the Sr. Director of CDP & Operations. PRIMARY DUTY: Design, implement, and support inclusive nature-based and outdoor learning experiences that are accessible to Frazer Center children, ensuring that every learner—including children with diverse developmental, sensory, physical, behavioral, and learning needs—can actively participate in meaningful, developmentally appropriate exploration of the natural world that promotes engagement, belonging, environmental awareness, and holistic development. MAJOR DUTIES AND RESPONSIBILITIES: ● Implement teacher training on the Nature Curriculum. ● Lead implementation of the Frazer Nature Curriculum Outreach Program to preschools from under-resourced communities. Ensure lessons are developmentally appropriate, hands-on, and rooted in exploration and inquiry. Continuously evaluate and improve outdoor learning environments. Stay current on research and best practices in outdoor education and early childhood inclusion. ● Serve as a resource to Frazer Center teachers during outdoor learning and activity. ● Develop safety protocols for outdoor learning that align with licensing, accreditation, and regulatory requirements. ● Collaborate with the Director of Development on funding opportunities for the program. ● Collaborate with other Frazer Center staff on opportunities to promote Frazer Center’s environmental programming at conferences, through community partnerships, etc. ● Collaborate on development of the budget for expenditures related to environmental programming. ● Ensure care and maintenance of any equipment, materials, or supplies purchased. ● Perform other duties as assigned. PHYSICAL FUNCTIONS ● Must be able to lift, push, and pull a minimum of 50 pounds ● Ability to lift from floor to chest level ● Ability to reach, bend, and stand for long periods of time ● Comfortable working outdoors in a variety of weather conditions ORGANIZATIONAL RELATIONSHIPS Reports to and is under the direct supervision of the Sr. Director of Child Director of Child Development Programs and Operations, Curriculum Coordinators, and additional ancillary personnel as appropriate. EXPERIENCE AND/OR EDUCATIONAL REQUIREMENTS: ● At least 3 years of environmental education / nature-based learning experience ● Minimum of a BA/BS in education, biology, environmental education, or other related field ● Sense of humor, flexibility, and creative “think outside the box” solution-based mindset ● Experience in early childhood settings, and knowledge of developmentally appropriate practice for children 6 weeks to 5 years’ old ● Experience working in inclusive settings for children and/or adults with disabilities ● Demonstrated professionalism and strong work ethic ● Strong oral and written communication skills ● Must pass mandatory criminal background checks and drug screen

Job Description THE MORGAN OLIVER SCHOOL Welcome Allies, Activists, Organizers & Liberators. Science Teacher Part-Time · Approximately 16 hours/week · Two to three days Position Overview The Morgan Oliver School is seeking a dedicated and passionate Science Teacher to bring science to life across our whole school — from our youngest learners through our Liberators middle school cohort. The ideal candidate is comfortable adapting instruction for very different ages and genuinely enjoys collaboration. The anchor of this role is an extended STEM morning with our Liberators, co-planned with our Middle School Lead, so a love of problem-solving and building things together is essential. This part-time position is approximately 16 hours per week over two to three days: roughly 7 hours of teaching across our four cohorts (K/1, 2/3, 4/5, and the Liberators), four hours of guaranteed weekly planning and collaboration time, and the remainder spent supporting the wider school day. The Liberators meet for a longer block than the lower grades. Responsibilities • Develop and deliver engaging science lessons aligned with NGSS (Next Generation Science Standards) for our four cohorts: K/1, 2/3, 4/5, and our Liberators middle school group., • Lead an extended STEM morning with the Liberators, partnering closely with the Middle School Lead to develop curriculum, brainstorm ideas, and plan trips and hands-on experiences together., • Use The Morgan Oliver School's scope and sequence to design age-appropriate curriculum that supports scientific inquiry across every cohort., • Incorporate hands-on activities, experiments, and projects to foster a love for science and enhance learning outcomes., • Assess student progress and adjust instructional strategies to meet individual needs and learning styles., • Collaborate with other educators to integrate science across the curriculum and promote interdisciplinary learning., • Maintain a positive and inclusive classroom environment that supports the social, emotional, and academic growth of all students., • Communicate regularly with parents/guardians regarding student progress, achievements, and areas for growth in science., • Support the wider school day alongside teaching — including recess duty and other shared tasks — as a present, contributing member of our small staff., • Participate in professional development opportunities and school-wide initiatives as required. Qualifications • Bachelor's degree in Science Education, Biology, Chemistry, Physics, or a related field (Master's degree preferred)., • State teaching certification or licensure (preferred)., • Proven experience teaching science to elementary and/or middle school students., • Knowledge of NGSS and experience with curriculum development and implementation., • Comfort with project-based, collaborative STEM work and a willingness to co-plan and problem-solve alongside colleagues., • Strong organizational skills and the ability to manage time effectively., • Excellent communication and interpersonal skills to collaborate with colleagues, parents, and students., • Commitment to fostering a diverse, equitable, and inclusive learning environment. Benefits • Competitive hourly rate of $40–50, depending on experience., • Four hours of guaranteed, protected planning and collaboration time each week., • Professional development opportunities to support ongoing growth and learning., • Supportive and collaborative work environment within a progressive educational institution., • Materials and budget provided to enhance classroom instruction and student engagement. To apply, contact admissions@mosatl.org · 468 Moreland Ave SE, Atlanta, GA 30316

Job Description Openwork is currently engaged in a search to find a motivated Quality Control Technician in Atlanta, GA. In this fast-paced, dynamic role, you will be responsible for conducting various lab and sensory tests while working closely with plant management, employees, and customers to ensure high-quality production standards. Apply today if you meet the qualifications listed below. In a Quality Control Technician job youll be responsible for: Conducting titratable salinity, titratable acidity, pH, viscosity, and other sensory tests Performing rapid microbiological testing after training Spending part of your day on the production floor to ensure products are correctly prepared and shipped Collaborating with upper management and R&D teams Interacting with customers and assisting with other tasks as assigned by management What youll need: Degree in a science field such as Chemistry, Biology, Food Science, or related discipline Flexibility to work both in the lab and on the production floor Strong attention to detail and ability to work in a fast-paced environment Perks: Competitive pay: $21/hour Health, dental, vision, and life insurance Paid time off In-person, full-time position: 8 AM 5 PM Click on Apply Now to be considered for this Quality Control Technician job in Atlanta, GA, or visit our website www.openwork.com to search for other opportunities that are currently available. About Openwork: Openwork is a talent-first staffing company on a mission to bring ease and thoughtfulness to an industry weve held a footing in for 50+ years. We believe theres more to life than livelihood, but that finding your dream career or team is a really good place to start. Our family of companies also includes QS Nurses and Aerospace Solutions. Looking for your dream job or hire? Visit us at www.openwork.com to say hello and start building your future, together. EOE \nCompany Description Openwork is a candidate-focused staffing company on a mission to bring ease, accessibility, and thoughtfulness to an industry we’ve held a footing in for 50+ years. We believe there’s more to life than livelihood, but that finding your dream job, career, or team is a really good place to start. Openwork is a candidate-focused staffing company on a mission to bring ease, accessibility, and thoughtfulness to an industry we’ve held a footing in for 50+ years. We believe there’s more to life than livelihood, but that finding your dream job, career, or team is a really good place to start.

Job Description Position: Environmental Laboratory Analyst I Location: 2480 Maner Rd.SE, Atlanta, GA 30339 Duration: 3 Months Client: Georgia Power Job Summary Southern Company Services is seeking an Environmental Laboratory Analyst I to support environmental testing and laboratory operations. This entry-level role is responsible for preparing and analyzing environmental samples, maintaining laboratory documentation, and supporting compliance with federal, state, and local environmental regulations. The ideal candidate will have a strong science background, attention to detail, and a commitment to laboratory safety and quality. Key Responsibilities · Prepare environmental samples for laboratory analysis, including logging, weighing, spiking, and sample preparation. · Perform laboratory testing using standard analytical techniques and equipment. · Receive, inspect, log, and process customer samples. · Prepare sample kits and support shipping and receiving activities. · Maintain accurate laboratory records and environmental documentation. · Follow laboratory safety procedures and support environmental compliance initiatives. · Assist with emergency response procedures for environmental incidents and spills. · Collaborate with laboratory staff to ensure accurate and timely test results. Required Qualifications · Bachelor's degree in Chemistry, Biology, Microbiology, Environmental Science, or a related field (Associate degree also considered). · Entry-level position (laboratory experience through education or internships is a plus). · Basic laboratory skills, including pipetting, weighing, measuring volumes, and laboratory safety. · Strong analytical, organizational, and problem-solving skills. · Excellent written and verbal communication skills. · Ability to work independently and as part of a team. Preferred Skills Environmental Laboratory • Chemistry • Biology • Microbiology • Environmental Science • Sample Preparation • Laboratory Testing • Laboratory Safety • Analytical Techniques • Environmental Compliance • Documentation • Quality Control • Sample Management

Job Description PerkinElmer has partnered with Hueman to find a Full-Time Field Service Engineer in Atlanta, GA. The Field Service Engineer provides highly visible customer support through the performance of on-site installation, as well as overseeing any necessary diagnoses, troubleshooting, service, and repair of complex equipment and systems. The Field Engineer will instruct customers in the operation and maintenance of the system and serve as company liaison with customer on administrative and technical matters for assigned projects. This role may include any aspect of field support, and is not limited to system hardware and software, PCs, and networking/wireless networking. PerkinElmer is a leading, global provider of technology and service solutions that help customers measure, quantify, detect, and report in ways that help ensure the quality, safety, and satisfaction of their products. For 85 years, PerkinElmer has pushed the boundaries of science in our food, industrial, life science and environmental markets. In addition to innovative laboratory technologies, our OneSource services division delivers a highly trained, experienced, and collaborative team of service engineers with solutions scalable and customizable to serve laboratory needs. Job Responsibilities: • Perform installations, maintenance, validations, and repairs while ensuring compliance with PerkinElmer’s service standards and key performance indicators, • Engage with customers to understand their analytical workflows and tailor service offerings, including training, support, and upgrades., • Enhance account profitability through efficient service execution and by identifying revenue opportunities such as billable work, consumables, and service leads, • Maintain assigned assets, including tools, test equipment (MTE), telecommunication equipment, and service parts inventory., • Enhance PerkinElmer’s product quality by proactively reporting improvement opportunities via the quality notification process., • Attend higher level certification through participation in company sponsored training & development offerings, • Complete all administrative tasks, including but not limited to time reporting and assigned training., • Maintain training and compliance in areas of health and safety, security, environmental and operational aspects of daily activities in the working environment Job Qualifications: • BA Bachelor Degree in Applied Science, Biology, Chemistry, Electronics, Mathematics, Engineering, or related discipline including military experience plus 3 years direct experience with repair of laboratory equipment OR, • Associate Degree in Applied Science, Biology, Chemistry, Electronics, Mathematics, Engineering, or related discipline including military experience plus 5 years direct experience with repair of laboratory equipment OR, • High School Diploma plus 7+ years direct experience with repair of laboratory equipment, • Outstanding interpersonal, written, and verbal skills, demonstrating the ability to communicate information clearly and accurately., • Technical critical thinking skills and attention to detail., • Outstanding customer service skills complemented by an ability to listen to and interpret client requests., • Aptitude for technical and practical matters., • MS Office skills: Outlook, PowerPoint, Word., • Excellent team player with a customer satisfaction focus, • Ability to follow and create written and verbal directions, read and understand technical bulletins and service manuals, work under time constraints, maintain alertness and concentration, and work safely with potential hazard Preferred Qualifications: • Detailed knowledge of analytical equipment, laboratory environment, and/or instrument control software, • Vendor issued certification on relevant laboratory equipment, • Knowledge of laboratory safety practices as defined by the Company and/or the customer’s site safety code, • Ability to travel by air, vehicle and/or other means of transportation as business requires. Travel will vary depending on territory requirements and/or customer base typically up to 50% of the time. (Car, laptop, and phone are company provided)., • Valid driver’s license and safe motor vehicle operation. AT PERKINELMER, WE BELIEVE IN THE POWER OF SCIENCE TO TRANSFORM OUR WORLD We partner with scientists, clinicians, lab technicians, engineers, and food producers globally to empower them with reliable and compelling scientific insights they need to accelerate the development of ground-breaking products, and laboratory solutions that improve the quality of our lives. By drawing on the ingenuity, creativity, and passion of our people, together, we enable our customers to fulfil their mission towards a healthier, safer, and more sustainable world. Hueman is proud to partner with PerkinElmer as the exclusive recruitment partner for this role. If you are interested in learning more about a career with PerkinElmer as a Field Service Engineer, apply today!

Job DescriptionCompany Description Deciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines and providing hope to people living with cancer, neurologic and autoimmune disease. Deciphera is leveraging its proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative medicines. In addition to advancing multiple product candidates from Deciphera’s platform in clinical studies, QINLOCK® (ripretinib) is Deciphera’s switch-control kinase inhibitor approved in many countries including the European Union and the United States for the treatment of adult patients with advanced gastrointestinal stromal tumor (GIST) who have received prior treatment with 3 or more kinase inhibitors, including imatinib. ROMVIMZA® (vimseltinib) is a kinase inhibitor approved in the United States for adult patients with symptomatic tenosynovial giant cell tumor (TGCT) for which surgical resection will potentially cause worsening functional limitation or severe morbidity, and in the European Union for adult patients with TGCT associated with clinically relevant physical function deterioration and in whom surgical options have been exhausted or would induce unacceptable morbidity or disability. The spirit of collaboration that has brought medications to life continues to guide how we operate, grow, and discover new breakthroughs. We cultivate an inclusive culture that values curiosity, creativity, and shared accountability—empowering individuals to challenge the unknown together. Deciphera offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance and a flexible spending account for either health care and/or dependent care. Job Description The Oncology Territory Manager is responsible for driving commercial performance within an assigned geographic territory by developing and maintaining professional relationships with oncology healthcare providers. This role executes brand strategy at the territory level through compliant, high‑quality scientific and product education, supporting appropriate patient identification and access. The Oncology Territory Manager operates independently in the field while collaborating cross‑functionally to deliver insights that inform business strategy, all in accordance with FDA regulations, company policies, and industry codes of conduct. Key Responsibilities: Territory & Account Management (50%) • Develop and execute a comprehensive territory business plan aligned with brand strategy, business objectives, and compliance requirements, • Identify, prioritize, and engage oncology accounts, including oncologists, advanced practice providers, pharmacists, and key office staff, • Deliver accurate, balanced, and approved product information, clinical data, and disease state education in a compliant manner, • Manage account interactions to support appropriate product utilization within approved indications, • Analyze territory performance data to adjust strategy and optimize call planning and resource allocation Cross‑Functional Collaboration & Field Insights (25%) • Collaborate with Market Access, Medical Affairs, Sales Leadership, and other internal stakeholders to support patient access and education efforts, • Communicate field‑based insights related to customer needs, market dynamics, competitive activity, and reimbursement trends, • Participate in internal meetings, training programs, and business reviews as required Administrative, Reporting & Compliance Activities (20%) • Maintain timely and accurate documentation of customer interactions, call activity, and territory plans within the CRM system, • Complete expense reporting, sample accountability (if applicable), and other administrative requirements in accordance with company policy, • Ensure strict adherence to FDA regulations, company SOPs, and industry compliance standards, including promotional practices Other duties and responsibilities as assigned Qualifications • Bachelor’s degree required, • Minimum of 5+ years of pharmaceutical or biotechnology sales experience, with oncology experience required, • Demonstrated ability to work independently in a field‑based role with limited supervision, • Strong understanding of compliant promotion within a regulated environment, • Valid driver’s license and ability to travel extensively within the assigned territory Preferred Capabilities • Prior oncology specialty sales experience in a small‑to‑midsize biotech or emerging company environment, • Knowledge of oncology treatment landscapes, clinical pathways, and reimbursement considerations, • Proven ability to interpret data and translate insights into effective territory strategies, • Excellent communication, presentation, and relationship‑building skills, • Strong organizational skills with the ability to manage multiple priorities effectively Additional Information Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $199,000-$243,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location. Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable) Benefits: • Competitive salary and annual bonus., • Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more., • Generous parental leave and family planning benefits., • Outstanding culture and opportunities for personal and professional growth. EQUAL EMPLOYMENT OPPORTUNITY INFORMATION Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.

Job Description CorDx is a leading biotechnology company that specializes in the development, manufacturing, and distribution of innovative diagnostic solutions. We are looking for a highly motivated and detail-oriented Production Coordinator to support the production team in delivering high-quality products to our clients. As a Production Coordinator, you will work closely with the production team to ensure that all manufacturing processes are carried out smoothly and efficiently. You will also be responsible for organizing and maintaining production schedules, monitoring inventory levels, and coordinating with various departments to ensure timely delivery of products to our customers. Responsibilities • Develop and maintain production schedules to ensure timely delivery of products to customers, • Monitor inventory levels and coordinate with purchasing department to order materials and supplies for production, • Collaborate with manufacturing team to develop and implement production plans, • Oversee the production process from start to finish, ensuring that all products meet quality standards and are delivered on time, • Communicate with various departments to ensure smooth flow of production process, • Resolve any production-related issues in a timely and effective manner, • Evaluate and improve production processes to increase efficiency and reduce costs Requirements • Bachelor's degree in a relevant field such as biotechnology, chemistry, or biology, • 2+ years of experience in a production coordination role preferably in the biotechnology industry, • Strong analytical skills and attention to detail, • Excellent communication and interpersonal skills, • Ability to work well in a team-oriented environment, • Proficient in Microsoft Office Suite, especially Excel, • Knowledge of cGMP regulations and ISO 13485:2016 is preferred., • Mandarin speaking preferred Benefits • Health Care Plan (Medical), • Retirement Plan, • Paid Time Off, • Training & Development, • Company Sponsored Meals, • Individual and Team Bonding Spending

Job Description Bioinformatics/Data Analytics Engineer Chippewa Government Solutions (CGS), a Sault Tribe Inc. (“STI Federal”) company, is searching for a dynamic and skilled Bioinformatician to be a key part of our expanding team! Who We Are & What We Do… At STI Federal, we drive growth through strategic government contracting, fulfilling our mission to support the Sault Ste. Marie Tribe of Chippewa Indians. Our company reinvests 100% of its profits into tribal businesses or community programs, enhancing the well-being of nearly 50,000 tribal citizens. Our work empowers federal agencies and strengthens some of the nation’s most critical initiatives, while fostering opportunities for skilled professionals to make a meaningful impact. What You’ll Do… The Bioinformatician will support the Influenza Division of the Center for Disease Control (CDC) in Atlanta, Georgia. The incumbent will provide computational biology support and bioinformatics services to enhance laboratory data management and analysis activities. This position is crucial for advancing the understanding of immunity to influenza through data-driven insights. Key Responsibilities & Expected Outcomes • Enhanced Data Management - Collect, analyze, and manage biological data to improve laboratory data accuracy and efficiency., • Optimized Application Development - Design, program, test, and maintain bioinformatics applications, ensuring they meet operational and research needs., • Streamlined Database Systems – Plan, develop, and maintain SQL and NoSQL database systems (e.g., Hadoop, Cassandra) while establishing quality metrics for sequencing workflows., • Standardized Protocols – Collaborating with others, create and document Standard Operating Procedures (SOPs) for analytical methods, application development, and script implementation., • Advanced Data Insights - Model and visualize data to support decision-making and contribute to scientific publications and presentations. Knowledge, Skills, & Abilities for Success • Demonstrates a dedication to upholding and enhancing STI Federal’s core values., • Excels in a collaborative team environment, fostering positive relationships and contributing to shared goals with professionalism and mutual respect., • Expertise in Phylogenetic, R, Python, Java, SQL, Tableau, PERL, Hadoop, and Cassandra., • Up-to-date knowledge of bioinformatics, genomics, metagenomics, virology, and immunology., • Proven ability to develop bioinformatics tools, workflows, and applications., • Experience with algorithm development and computational pipelines., • Strong verbal and written communication skills to translate technical concepts into actionable insights. Minimum Qualifications • Master’s degree in biomedical sciences or related field, with classes/training in microbiology, genomics, ecology, and evolution., • 6+ years in bioinformatics or related role. Preferred Qualifications • Master’s or PhD in Biomedical Sciences, Bioinformatics, Data Analytics, Computer Science, or a related field., • Additional experience in computational methods and algorithm development, AI and machine learning is highly valued., • Familiarity with CDC-related research or public health initiatives is a plus. Compensation & Work Environment • Salary Range: $90,000 - $105,000 dependent on experience., • Environment: Work will be performed at the CDC Roybal Campus in Atlanta, Georgia. STI Federal is an Equal Employment Opportunity Employer. We are committed to creating a diverse and inclusive workplace. Qualified applicants are considered for employment regardless of age, disability, ethnicity/race, national origin, religion, gender, gender identity, sexual orientation, or veteran status. Native American preference applies when candidates meet qualifications equally. STI Federal participates in the Electronic Employment Verification Program. Learn more about E-Verify.

Job Description About Bestzyme: Through advanced enzymes and synthetic biology, Bestzyme enhances the natural world and creates a quality life. At Bestzyme, we're committed to accelerating sustainable and efficient industrial solutions to meet the demands of our evolving world. We understand the importance of nurturing science not just for today, but for preserving tomorrow. Our aim is to help make people and nature thrive in harmony through the incredible power of biotechnology. Founded in 2013, Bestzyme is a proud subsidiary of GenScript. Our accomplished team is driven to harness the power of biotechnology to accelerate sustainable and efficient solutions for biofuel, food & beverage, distilling, starch, household care, textile, animal feed industries and functional proteins. We produce innovative industrial enzymes that deliver performance and scalability for your production needs. With our cutting-edge synthetic biology expertise, we create solutions tailored to your industry's burgeoning demands. We believe in the strength of collaboration to foster industrial growth and environmental sustainability. Position: Sales Manager (Sweet Protein) Location: United States – Remote The estimated salary range is $100,000 - $130,000 based on experience level. Key Responsibilities： 1. Execute the business strategy and annual plan developed by the department, focus on business opportunities and organize resources to achieve annual sales budget and profit budget., 2. Build and maintain strong relationships with potential customers and partners through proactive communication and regular visits to discuss commercial opportunities in full autonomy, 3. Maintain and continuously improve understanding of products, applications and markets. Share the insight and knowledge with internal team to optimize product development, 4. Collaborate with cross-functional teams (including technical and production teams) and responsible for driving sales and business development efforts in North/South America to achieve sustainable growth in the food ingredient line., 5. Working with customers and partners to generate market insight of customer needs and industry trends to support build market strategy for new product launch., 6. Complete temporary important tasks assigned by superiors., 7. Be results driven and show strong sales acumen Qualifications： 1. Bachelor degree or above and minimum 5-6 years of relevant B2B sales or business development experience in food ingredients, food & beverage, sweetener or flavor ingredient industry;, 2. Proven experience in key account management and channel development; Excellent negotiation and communication skills; High level of autonomy and the ability to work independently;, 3. Proven success in building relationships with professionals at all organizational levels with internal and external customers; Able to better grasp the customer's psychology, understand and can effectively use sales skills;, 4. Market knowledge and insight for the Food & Beverage/ Ingredients space;, 5. Strong ability to resist pressure and learning ability, 6. Strong communication skills Mandarin - speaking (Bilingual preferred) #LI-IP1 #GS US Benefits: Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work. Bestzyme is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Bestzyme maintains a drug-free workplace. Please note: Bestzyme will only contact candidates through verified application sources. Bestzyme does not request personal information from candidates through individual email or any other platform.

Job Description Earth Smart Environmental Solutions, LLC is seeking an Environmental Field Chemist to collect, identify, and package/lab pack various hazardous/non-hazardous waste and transport in accordance with EPA and DOT regulations. Other essential functions and responsibilities include: • Maintain knowledge and training of job aspects, • Undertake responsibility and compliance of jobsite, • Manage services and ensure client/customer needs are met or exceeded, • Work as part of team and provide leadership Qualifications: BS Degreed science curriculum (Chemistry, Environmental, Biology or other with General and Organic Chemistry) or industry related experience Preferred / Not Required Lab packing experience Preferred/Not Required Class A or B CDL with HAZMAT Endorsement considered a plus but Not Required Ideal candidate will be able to lift 50 pounds Clean Driving Record Veterans Preference - encouraged to apply Compensation based on experience \nCompany Description Earth Smart Environmental Solutions (ES2) is a Service-Disabled Veteran Owned Small Business that provides recycling, reuse and/or disposal of hazardous, universal, medical, pharmaceutical, non-hazardous, and solid waste while meeting or exceeding customer expectations for all of the United States. ES2 follows all local, state, and federal requirements and has maintained zero safety finding or notice of violations. ES2 is an equal opportunity employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity, or any other characteristic protected by law. Service members and veterans, and the spouses and family members of the service members and veterans are encouraged to apply. Earth Smart Environmental Solutions (ES2) is a Service-Disabled Veteran Owned Small Business that provides recycling, reuse and/or disposal of hazardous, universal, medical, pharmaceutical, non-hazardous, and solid waste while meeting or exceeding customer expectations for all of the United States. ES2 follows all local, state, and federal requirements and has maintained zero safety finding or notice of violations. ES2 is an equal opportunity employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity, or any other characteristic protected by law. Service members and veterans, and the spouses and family members of the service members and veterans are encouraged to apply.

Job Description Immediate W2 contract position available in Atlanta, GA. Estimated Duration: 7 months Job Description: An Environmental Laboratory Analyst is responsible for gathering, monitoring and testing of environmental samples to determine the presence of pollutants and other contaminants. They collect samples from various sources, such as air, water, and soil, analyze them using specialized equipment and techniques. They play a critical role in ensuring compliance with federal, state, and local environmental regulations. Key Responsibilities: • System Monitoring: Monitor environmental systems, such as wastewater treatment, air pollution control, and waste management., • Environmental Compliance: Monitor and ensure compliance with local, state, and federal environmental regulations, permits, and standards relevant to the organization's operations., • Data Analysis: Collect and analyze environmental data, including air and water quality data, to assess environmental conditions, trends, and system performance., • Emergency Response: Knowledge of emergency response plans for environmental incidents, spills, and accidents., • Environmental Documentation: Maintain accurate records, permits, and documentation required for environmental compliance and reporting. Qualifications: • Education: Bachelor’s degree in Chemistry, Biology, Microbiology, Environmental Sciences or Associate’s degree in Chemistry, Biology, Microbiology, or Environmental Sciences, • Experience: Several years of experience in environmental monitoring and testing, with a strong understanding of environmental regulations and industrial processes., • Environmental Regulations: Profound knowledge of local, state, and federal environmental regulations, permits, and standards., • Technical Skills: Proficiency in environmental monitoring equipment, data analysis tools, and environmental modeling software., • Communication: Effective communication skills, both written and verbal, to convey technical information and compliance requirements., • Problem-Solving: Strong problem-solving abilities to address complex environmental challenges and recommend innovative solutions., • Attention to Detail: Meticulous attention to detail to ensure accuracy in environmental documentation and regulatory compliance., • Teamwork: Ability to collaborate effectively with colleagues, stakeholders, and multidisciplinary teams to achieve environmental goals., • Analytical Skills: Strong analytical thinking to assess environmental data, identify trends, and make informed recommendations.\nCompany Description We provide supplemental employees to the region's most sought after power projects. We credit our success to the commitment we show to our job applicants. E Group Recruiters are here to make sure your job search experience is the best it can be. Our recruiters are experts in knowing what the client manager is looking for in a resume, what bill rate the market will bear, and how to make your application stand out among the rest. Our personal touch continues even after we've found the perfect job for you. All full-time employees are eligible to pay for full health and retirement benefits including BC/BS health and dental insurance, life and disability insurances, and 401K with an immediately vested match is available. We have a dedicated team to guide you through these benefits. We provide supplemental employees to the region's most sought after power projects. We credit our success to the commitment we show to our job applicants. E Group Recruiters are here to make sure your job search experience is the best it can be. Our recruiters are experts in knowing what the client manager is looking for in a resume, what bill rate the market will bear, and how to make your application stand out among the rest. Our personal touch continues even after we've found the perfect job for you. All full-time employees are eligible to pay for full health and retirement benefits including BC/BS health and dental insurance, life and disability insurances, and 401K with an immediately vested match is available. We have a dedicated team to guide you through these benefits.

Job Description Job Description ** Johnson Service Group (JSG) is a nationally recognized professional staffing and recruiting firm that is looking for an experienced Environmental Laboratory Analyst to fill a seven-month contract assignment in the Atlanta, GA area. This position may require some bending, lifting, climbing, prolonged sitting, prolonged walking, walking on gravel or crawling when necessary. · US Citizenship · No per diem · Local candidates only Environmental Laboratory Analyst 1 Work Location: Atlanta, GA · PPE: Laboratory safety PPE, to include close-toed shoes, lab coat, eye protection, gloves - all lab provided · Job hazard analysis - may be exposed to hazardous chemicals to include but not limited to acids and bases, coal and oil, high temperature ovens and hot blocks. · An Environmental Laboratory Analyst is responsible for gathering, monitoring and testing of environmental samples to determine the presence of pollutants and other contaminants. · They collect samples from various sources, such as air, water, and soil, analyze them using specialized equipment and techniques. · They play a critical role in ensuring compliance with federal, state, and local environmental regulations. · Position is responsible for providing support for routine analyses and laboratory operation. This includes, but is not limited to, wet chemistry procedures and analysis, coal and oil analysis, radiochemistry analysis, instrumental analysis, sample preparation, cleaning of glassware, Sample Receiving support (sample login, disposal, etc.), procedure review and revision. QUALIFICATIONS Education: · Bachelor’s degree in Chemistry, Biology, Microbiology, Environmental Sciences · Associate’s degree in Chemistry, Biology, Microbiology, or Environmental Sciences Experience: · Several years of experience in environmental monitoring and testing, with a strong understanding of environmental regulations and industrial processes. Environmental Regulations: · Profound knowledge of local, state, and federal environmental regulations, permits, and standards. Technical Skills: Proficiency in environmental monitoring equipment, data analysis tools, and environmental modeling software. Communication: · Effective communication skills, both written and verbal, to convey technical information and compliance requirements. Problem-Solving: · Strong problem-solving abilities to address complex environmental challenges and recommend innovative solutions. Attention to Detail: · Meticulous attention to detail to ensure accuracy in environmental documentation and regulatory compliance. Teamwork: · Ability to collaborate effectively with colleagues, stakeholders, and multidisciplinary teams to achieve environmental goals. Analytical Skills: · Strong analytical thinking to assess environmental data, identify trends, and make informed recommendations. KEY RESPONSIBILITIES System Monitoring: · Monitor environmental systems, such as wastewater treatment, air pollution control, and waste management. Environmental Compliance: · Monitor and ensure compliance with local, state, and federal environmental regulations, permits, and standards relevant to the organization's operations. Data Analysis: · Collect and analyze environmental data, including air and water quality data, to assess environmental conditions, trends, and system performance. Emergency Response: · Knowledge of emergency response plans for environmental incidents, spills, and accidents. Environmental Documentation: · Maintain accurate records, permits, and documentation required for environmental compliance and reporting. Is this position supporting a government-related project? No Does this position require driving (excluding commute)? YNo Does this position require personal protective equipment (PPE)? Yes Estimated Start Date: 11/16/2026 Estimated Duration of Job Assignment: 06/14/2027 JSG offers medical, dental, vision, life insurance options, short-term disability, 401(k), weekly pay, and more. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law. #D650 \nCompany Description Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 40 years of experience investing in people and companies. We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs. We offer medical, dental, vision, life insurance options, paid time off, 401(k), weekly pay, and more. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 40 years of experience investing in people and companies. We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs.\n\nWe offer medical, dental, vision, life insurance options, paid time off, 401(k), weekly pay, and more.\n\nJohnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.\n

Job Description Job Description: • This position will perform dosimetry analysis to include Optically Stimulated Luminescence (OSL) and electronic dosimeters (EPD) as well as associated quality control tasks., • Contract position will provide task/processing assistance to the dosimetry section so to ensure efficiency and compliance for nuclear customers. Education and Desired Qualification: • BS degree in Biology, Chemistry, or related science is preferred., • Must be able to work within a team environment and be a good listener., • Must be detail-oriented, self-directed and possess good organizational skills., • Experience with quality control requirements for processing methods., • Computer proficiency using instrument and data management software., • Prepare, process, and ship dosimeters under the guidance of senior analyst., • Experience with Thermo Luminescent Dosimeters (TLD) will also be taken into consideration., • This is an onsite position, no hybrid options.

Job Description Remote GMP Quality Mgr needs 8+ years of experience required, with relevant experience in biotech or pharmaceutical industry with most experience in a Quality role. Advanced knowledge of GMP manufacturing and/or market release of pharmaceutical dosage forms and/or combination products. Experience with managing external CMOs, contract laboratories, and third-party logistics suppliers. Must have experience in reviewing and approving master and executed batch records and performing final disposition of drug substances and products. Experience managing quality events (investigations, CAPA and change control), and working knowledge of formal risk management tools and assessments. The individual must demonstrate the ability to evaluate and assess technically complex quality events, as well as the ability to document these events with excellent technical writing skills. Experience in evolving GMP related quality systems, policies, and procedures to ensure compliance with evolving standards as well as improving the efficiency of related workflows. Strong ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations. Excellent verbal and written communication skills, including ability to interact effectively with senior management, partners, and project core team members. Self-motivated, flexible, and able to prioritize work and handle multiple assignments in a fast-paced environment, while maintaining a high level of quality and compliance. Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering, pharmacy) or relevant field of study. Duties: Be the QA representative on cross-functional project teams. Responsible for communicating with the Quality and Production departments at domestic and international contract manufacturing organizations, and within SMPA's Quality, Supply Chain, CMC, and Commercial Manufacturing departments. Conducts product release activities for clinical and commercial drug substances and drug products; including review and approval of Master Batch Records, Executed Batch Records, release and stability testing documentation, and batch disposition. These activities must be conducted in a timely manner to ensure continued product supply while ensuring Quality and Safety of the product.

Job Description 2026 YTD Sales are at an all Time Record Level ! Water Treatment Chemical Service Technician—Atlanta, Georgia Garratt-Callahan (www.garrattcallahan.com) is family friendly, profitable, stable, and fiercely private. No layoffs in 120 years. No ownership changes in 120 years. Haven't changed our commission plan in 30 years. 80 straight years of profitability. We have operations in every state in the USA. Chemical Service Technicians are responsible for sales support by maintaining the existing customer base in Atlanta, Georgia. Perform water treatment tests at the existing customers primarily in the greater Atlanta area. With the freedom of working from your home, you can work and train in a territory alongside veteran Territory Managers. The best place to live is in or very near Atlanta. The career track for a Chemical Service Technician is to train to become a Territory Manager. Territory Managers are eligible for unlimited commission and a year-end bonus. As a Technical Sales Support/Service Technician, you will receive an industry-competitive salary, expenses, benefits, and a $675 per month car allowance. In addition, ample technical support is provided along with continuous training. Paperwork is kept to a minimum. Compensation is based upon experience and the ability to succeed. $60,000 to $80,000 first year for a qualified candidate. We hire with a focus that favors the committed employee both in terms of overall compensation and growth opportunities. We have designed our compensation package accordingly. Benefits available include a corporate 401k, health, dental, vision, and life insurance. Job Responsibilities: • Solve customers' water problems., • Treat industrial boilers and cooling towers to keep energy efficient and environmentally friendly., • Perform detailed water testing & analyses at Industrial sites, Manufacturers, Data Centers, Medical Centers, and Commercial Buildings., • Help sell Garratt-Callahan's proprietary chemical blends, equipment, & monitoring technology., • Passivation of stainless steel in industrial water treatment systems., • Help sell corrosion & scale inhibitors, coagulants, flocculants, biocides, bio-augmentation, feed & monitoring equipment, water management plans, reverse osmosis products., • Help sell Water Safety Programs., • Keep our existing customers happy., • Help bring on new industrial customers. About Garratt-Callahan: Garratt-Callahan is a US based private 120-year-old, nationwide water treatment chemical company. Garratt-Callahan www.garrattcallahan.com treats industrial boilers and cooling towers to keep them energy efficient and environmentally friendly with one of the most advanced product lines in the industry. We are registered to ISO 9001:2015 and sell an industry leading line of “green" solutions, G-C GreenTech. We are headquartered in Burlingame, California. G-C is family owned, profitable, and expanding. We have five chemical plants in the USA, technical salespeople in every state, and the Caribbean. Benefits: • We offer a competitive benefit package which includes medical, dental, vision, AD&D, LT, and 401k. A monthly car allowance and travel expenses are provided., • First year compensation is $60,000 to $80,000 depending on experience., • Advanced training, and a clear career path into sales., • Family friendly, flexible hours., • A huge benefit of working for Garratt-Callahan is our stability and low turnover., • No Layoffs in our 120-year history, • G-C is a profitable company. The last year that G-C did not turn a profit was during World War 2., • 2025 was a record sales year, and 2026 sales are trending to be even better. To Apply, please log on to: https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=16ed56fa-3af7-47fc-878a-c4d47df49e2f&ccId=19000101000001&jobId=572673&source=CC2&lang=enUS Thank you for considering Garratt-Callahan Company. Garratt-Callahan is an EEO/AAE employer. Minorities, women, veterans and individuals with disabilities are encouraged to apply. NOTE: Garratt-Callahan does not sponsor work visas. No recruiters please. Requirements: You will be a successful applicant if you have a technical degree such as Chemistry, Chemical Engineering, Biology, Mechanical Engineering, Paper Science, or Water Resources. Nice to have backgrounds include: lab experience, field service, plumbing, pipe fitting, welding, HVAC, electric. One-year technical sales, or an internship related to water treatment chemicals is preferred, but we are willing to train and mentor. Outside industrial sales experience is a plus. You must live in Atlanta or very nearby and be familiar with the industrial marketplace of the area. NOTE: Garratt-Callahan does not sponsor work visas. No recruiters please. If you have a disability, and need assistance during the application and selection process as a result, please contact the Garratt-Callahan Human Resources department at 650.697.5811. Arrangements can be made to provide an accommodation in order to assist you in applying for an open position using our on-line system, completing any other related paperwork, interviewing, or any other portion of the employment process. When requesting an accommodation, please provide your name, phone, email address, or any other means of contacting you. Provide a brief description of the nature of the requested accommodation. A member of the Human Resources team will then contact you to discuss your request. A request for an accommodation will not affect your opportunities for employment with Garratt-Callahan. Garratt-Callahan values differing experiences, backgrounds and perspectives among our employees, and see them as a competitive advantage. Garratt-Callahan is committed to the fair and equal treatment of all associates and applicants. Garratt-Callahan is an equal opportunity employer that evaluates qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. • The “Equal Employment Opportunity is the Law” poster is available at: http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf • Garratt-Callahan Company’s reaffirmation of Equal Employment/Affirmative Action Statement http://www.g-c.com/documents/humanresources/EEOLetterJeffGarratt.pdf Key Words: Chemistry, chemicals, scientific, science, salesperson, salesman, saleswoman, outside sales, technical sales, account representative, account executive, territory sales, territory manager, district sales, district manager, field engineer, field service, AE, sales engineer, data center, chemical engineer, chemist, mechanical engineer, biologist, biology, microbiology, nalco, ecolab, Global Water, Veolia, us water, Suez, chemtreat, industrial water engineering, solenis, Meras, chem-aqua, kurita, evoqua, fremont, water treatment, boilers, cooling towers, waste water, pumps, equipment, chillers, polymers, biocides, Atlanta. Marietta, Gainesville, Fayetteville, Carrollton, Conyers, Athens.

Job Title: Food Quality Safety Compliance Manager - Retail Division Job Location: Charlotte-USA-28219, Atlanta-USA-30344, Denver-USA-80249, Orlando-USA-32827, Phoenix-USA-85040 Work Location Type: On-Site Salary Range: $87,000.00 - 120,000.00 Since 1942, SkyChefs has taken culinary excellence to new heights. As a trusted partner to the nation’s leading airlines and retailers, we proudly deliver millions of meals and exceptional service experiences every year across 43 sites throughout the United States. Built on a legacy of operational excellence, culinary expertise, and continuous innovation, we are committed to setting the industry standard in aviation culinary, airline services, last-mile logistics, and retail commerce. From the kitchen to the runway, our teams work together to deliver quality, reliability, and service at every altitude. Our people are the heart of everything we do. At SkyChefs, a career is more than a job – it’s an opportunity to grow, lead, and make an impact in a fast-paced, team-driven environment. Join America’s first, foremost, and finest and take your career to new heights. Join our Retail Division Quality team as a Food Quality Compliance Manager and help drive food safety, quality excellence, and regulatory compliance across a growing network of Ready-to-Eat manufacturing and retail locations across the U.S. This highly visible leadership role partners with operations, quality teams, customers, and suppliers to develop and strengthen Food Safety and Quality Management Systems, ensuring product integrity, compliance with FDA, USDA, and GFSI requirements, and adherence to customer and brand expectations. The ideal candidate is a collaborative leader who thrives in a fast-paced environment, builds strong partnerships across multiple locations, and is passionate about protecting both our customers and our brand. • Work Location: This position can be based at our HQ's in Irving, TX or at one of our retail division locations: Denver, CO, Charlotte, NC, Phoenix, AZ, Atlanta, GA, Orlando, FL., • Travel Requirement: This role requires approximately 60-70% travel to support teams in our locations across the U.S. Quality Assurance • Create, develop, maintain and communicate best-in-class food safety and quality management systems, • Measure supplier and CSC compliance to quality systems standards to identify and address high risk concerns through audit and inspections, • Lead improvement, corrective and preventative actions with US operations & market teams., • Provide technical and subject matter expertise as required., • Contribute to the design of new products, processes and procedures with risk assessments, establishing quality systems, defining quality requirements, qualifying new suppliers and writing, reviewing and approval of specifications., • Contribute to cost, capacity and contingency projects., • Provide coaching and training to CSC leadership on all food safety, quality and problem solving programs, as well as facilitation training of the Quality Systems, • Conduct assessments with emphasis in food safety, • Ensure customer requirements relevant to quality and food safety are met, • Conduct vendor inspections to qualify or verify vendors in conjunction with procurement, and assist with supplier accreditation and recalls when needed, • Provide monthly progress reports for distribution, • Participate and support company sponsored initiatives such as Lean Manufacturing, • Engage with Key Customers and provide leadership to ensure highest standards are met, • Evaluate the level of compliance to Food and Drug Administration (FDA) and USDA regulations, • Manage and maintain all documentation according to USDA, FDA and Company requirements, • Assist with the implementation of USDA, FDA and GQS components, • Participate and support company sponsored initiatives such as Lean Manufacturing, • Bachelor of Science in Food Science, Biology or related scientific/Food field, • Minimum 5-7 years’ experience in quality assurance, field operations or related food industry experience in managing Quality Assurance Programs, and/or Manufacturing Systems, • 3 plus years working with USDA facilities, • Direct experience with food labeling requirements, regulations and nutritional panels/compliance, • Experience in conducting external and internal audits, • Working knowledge of Hazard Analysis of Critical Control Points, (HACCP), Good Manufacturing Practices, (GMPs), ISO Standards, International food standards and regulations, BRC certification process, manufacturing best practices and continuous improvement and general microbiology, • Proactive problem-solving and creative decision-making skills, • Experience in team-based management and multi-unit environment, • Ability to facilitate groups and communicate effectively at all levels in the organization., • Strong oral, written and interpersonal skills with analytical, organizational and planning expertise, • Ability to facilitate groups and experience in writing training materials preferred, • Strong knowledge of Microsoft Office and Windows-based computer applications, • 60% – 70% domestic travel required to our U.S. facility/kitchen locations, • Initial training is conducted at SkyChefs corporate headquarters in Irving, TX Preferred Certifications • Preventive Controls Qualified Individual (PCQI), • Internal auditor certification (GSFI scheme), • HACCP and Seafood HACCP certification, • GFSI schemes certification such as BRC, FSSC 22000, SQF SkyChefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

Job Description Your studies in Health Science, Biology, Exercise Science, Kinesiology, or other science-related major coupled with a drive to help others is the perfect foundation to build a great career in Orthodontics! Discover the fun of working “hands-on” in a stable industry that offers a healthy workplace, positive relationships, and amazing work hours! No prior medical/dental industry experience required! Green Orthodontics, the private orthodontic practice of Dr. Noam Green, is growing! Our upbeat, close-knit team is seeking another delightful co-worker to add their smile and expertise to our group. What defines our practice? The people! We are a true team whose members share the value of doing our absolute best for each patient/parent that entrusts us with their care. Our patients are like family, and we want each visit to be a welcome “homecoming.” Could this be the career you are seeking? Do you prefer to “move around” at work and enjoy the idea of not having a “desk job”? Are you seeking work that offers a positive, mental challenge? How about a career that works with your hands, interfaces with children and adults, keeps you busy all the time, utilizes the coolest technology, manages meticulous details, and works in a team-based setting? Are you seeking work that allows you to see the measurable impact of your work from one patient’s visit to their next? Did you just say “YES!” out loud? Then, let us tell you more! How does training work? The position of “orthodontic assistant” encompasses a wide range of “on-the-job” trained skills from instrument sterilization/management, inserting and replacing wires, delivering “invisible braces,” giving braces instructions, cementing appliances, documenting records, re-bonding brackets, and all the while, to hearing the latest “knock-knock” joke from your 8-year-old patient who is laughing all the way through to the punchline! Green Orthodontics offers an organized, well-supported, in-office training program that begins with the most basic of skills and, over a series of planned weeks, introduces new learning goals as prior skills are mastered. Your focus and commitment impact your income; wages increase as each new learning module is introduced. What are the qualifications to apply? • A desire to work a full-time position (Monday - Thursday is your permanent work schedule. Yes, with rare exception, every weekend is a 3-day weekend and Thursdays end by 3:30PM!), • Prior customer-service experience and being at ease (and enjoying!) conversation with “most anyone of any age.”, • The right background. Which of these descriptions matches to you? Candidates with prior orthodontic experience are welcome to apply. We are also seeking candidates who have credit hours towards or who have earned a BS or BA in Exercise Science, Biology, Kinesiology, Health Science, Art Studio, or people-focused related major. Resumes of candidates with stable work experiences demonstrating customer service skills and professional or personal interests that demonstrate fine motor skills and excellent hand-eye coordination are also welcomed to apply., • Excellent, verifiable work-related references., • Computer friendly- software savvy aptitude with fast, accurate and detailed data entry., • Preference to have a career where you are NOT sitting in front of a computer for most of your workday! Orthodontic assistants are “on the move and up and own”; standing, walking, sitting, turning... this role is the right match to those who enjoy being active., • Initiative to study to learn terminology, processes, procedures, and software that are industry specific. TWO OPTIONS TO APPLY (read carefully, please!) • One option is to send your resume to us through Indeed., • If you find this post intriguing and you want to stand out and be noticed: Send your cover letter sharing why this job seems tailor-made for you, along with your resume, directly to our staffing consultant’s GMAIL written below in a format to prevent internet spam grabbers: HappyGeorgiaSmiles at GMAIL dot com Qualifying candidates will receive an email response from our Staffing Consultants Paige Healey or Carol Paige, with additional application information within 1-2 business days after emailing your resume and cover letter. Please check your junk and spam folder in case your security settings misdirect our attempt to reach you! (It happens!) To help us stay organized... Please, no resume drop-offs, calls, or faxes to our office. All Candidate applications are confidential.

Job Description Your background in Health Science, Biology, Exercise Science, Kinesiology, or another science-related field—combined with a genuine desire to help people—could be the foundation of an exciting career in orthodontics! Enjoy a profession with amazing work hours that keeps you moving, challenges you to learn, and allows you to work directly with patients every day. Quest Orthodontics, the private orthodontic practice of Dr. Arjun Patel, is growing! We’re looking for a friendly, energetic teammate who enjoys people, being coached, takes pride in their work, and wants to be part of a practice where the patient experience truly matters. Our team works together to give every patient and parent exceptional care while creating an environment that is positive, supportive, and fun. Could orthodontics be the career you’ve been looking for? If you’d rather be on your feet than behind a desk, enjoy working with your hands, love interacting with children and adults, and want a job that keeps you engaged throughout the day, this could be a great fit! You’ll use the latest technology, learn new skills, manage important details, and actually see the results of your work as patients progress through treatment. If you’re ready to trade the desk for a hands-on career, learn something new every day, and become part of a team that loves what it does, keep reading! What does an Orthodontic Assistant do? Quite a bit! Orthodontic assisting is a hands-on career with a variety of skills to master. You’ll learn everything from instrument sterilization and management to assisting with wires and appliances, providing instructions, documenting patient records, and more. You’ll also become part of the patient experience—helping patients feel comfortable, confident, and excited about their orthodontic journey. How does training work? Quest Orthodontics provides structured, supported, in-office training that starts with the fundamentals and introduces new skills as you become proficient. Your effort, focus, and commitment to learning will help determine how quickly you (and your wages!) grow in the position. What are the qualifications to apply? • A desire to work a full-time position (Monday-Thursday is your permanent work schedule. With rare exception, every weekend is a 3-day weekend!), • Prior customer-service experience and being at ease talking with people of all ages., • The right background. Prior dental or orthodontic experience is nice but not required! We welcome candidates with strong customer-service experience, science-related education, or backgrounds that demonstrate good hand-eye coordination and fine-motor skills., • Excellent, verifiable work-related references., • Computer friendly- software savvy aptitude with fast, accurate and detailed data entry., • Preference to have a career where you are NOT sitting in front of a computer for most of your workday! Orthodontic assistants are “on the move and up and down”; standing, walking, sitting, turning... this role is the right match to those who enjoy being active., • You should be dependable, detail-oriented, comfortable with technology, and willing to learn the terminology, procedures, and software unique to orthodontics. TWO OPTIONS TO APPLY (read carefully, please!) • One option is to send your resume to us through ZipRecruiter., • If you find this post intriguing and want to stand out and be noticed, send your resume and cover letter sharing why this job seems tailor-made for you directly to our staffing consultant’s GMAIL written below in a format to prevent internet spam grabbers: YourSmileExperts at GMAIL dot com Qualifying candidates will receive an email response from our Staffing Consultants, Paige Healey or Kelly Miller, with additional application information within 1-2 business days after emailing your resume. Please check your junk and spam folder in case your security settings misdirect our attempt to reach you! (It happens!) To help us stay organized... Please, no resume drop-offs, calls, or faxes to our office. All Candidate applications are confidential.

Job Description Job Description Job Title: Biologics Program Coordinator Department: Clinical Services Reports To: Director of Clinical Services FLSA Status: Exempt Approval Date: June 08, 2026 Summary The Biologics Program Coordinator oversees the operational, clinical, and administrative functions of the biologics and regenerative medicine program at Peachtree Orthopedics. This role serves as the subject matter expert for biologics offerings, coordinates patient care and procedures, manages inventory and equipment, supports research initiatives, and partners with physicians, clinical staff, vendors, and patients to ensure exceptional service, compliance, and program growth. Essential Duties and Responsibilities • Coordinate biologics procedures, appointments, and treatment schedules with physicians, patients, vendors, and facilities., • Serve as the primary point of contact for biologics vendors, representatives, physicians, staff, and patients., • Educate patients regarding biologics procedures, treatment options, pricing, aftercare, and expected outcomes., • Manage consent forms, patient documentation, and procedural compliance requirements., • Order, stock, maintain, and inventory biologics program supplies, injectables, and equipment., • Assist with inventory controls, charge capture, billing support, and reimbursement processes., • Train staff on biologics protocols, equipment operation, documentation standards, and authorization requirements., • Maintain biologics laboratory operations, including equipment maintenance, sterility, safety, and inventory management., • Prepare biologic products and assist providers during biologics procedures., • Apply post-procedure dressings, perform dressing changes, and support patient care activities as needed., • Ensure compliance with OSHA, HIPAA, infection prevention standards, and bloodborne pathogen regulations., • Manage patient participation and data entry for patient-reported outcomes programs and research initiatives., • Assist with clinical research activities, data collection, analysis, and reporting requirements., • Collaborate with leadership to identify opportunities for program growth, operational efficiency, and service excellence., • Other duties as assigned. Qualifications • Bachelor’s degree in Biology, Chemistry, Pre-Med, Healthcare, or related field preferred; or equivalent clinical certification (RN, LPN, Certified Lab Technician, or Certified Phlebotomist)., • Minimum one year of clinical, laboratory, or healthcare experience required., • Experience with biologics, regenerative medicine, phlebotomy, laboratory procedures, or orthopedic healthcare preferred., • Strong organizational, communication, customer service, and program coordination skills., • Ability to work independently while managing multiple priorities in a fast-paced environment., • Proficiency with Microsoft Office Suite and electronic medical record systems. Supervisory Responsibilities This position does not have direct supervisory responsibilities but may provide training, education, and workflow guidance to clinical staff participating in biologics program activities. Certificates, Licenses, Registrations • BLS Certification required., • RN, LPN, Certified Lab Technician, Certified Phlebotomist, or related clinical credential preferred. Physical Demands & Work Environment Regular standing, walking, lifting, patient interaction, laboratory activities, and clinical procedure support are required. Must be able to lift up to 50 pounds and perform blood draws, injections, and biologics preparation activities. Travel between Peachtree Orthopedics locations may be required. Peachtree Orthopedics is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description This position is responsible for providing a referral intake service for potential eye donors, presenting the option of donation and providing professional liaison service to hospitals and funeral homes to coordinate eye donor recoveries. All responsibilities are performed within the scope of GEB’s missions and values. The Donor Coordinator position is a critical one within the organization that affords a high level of personal fulfillment and employment satisfaction. -Respond to all incoming donor referral emails, faxes, and telephone calls. -Inform grieving families about donation options. -Communicate and dispatch Recovery Technicians. -Communicate with Supervisor On-Call, Organ Procurement Organizations (OPO), Tissue Banks, Medical Examiner/Coroners, Law Enforcement, Recovery Technicians, and Funeral Homes professionals regarding donors. -Complete donor records including data entry and obtaining/recording donor family authorizations. -Obtain medical/social history information from donor families, physicians, and hospitals/hospices. -Assist the department supervisor and manager in various assigned duties. -Adhere to the Eye Bank’s Policies and Procedures, Eye Bank Association of America Medical Standards, and US Food & Drug Administration regulations. -This is a night shift position. 3 shifts per week from 7 p.m. to 7 a.m. -Perform other duties as assigned. Qualifications: -Bachelor’s degree from an accredited university/college (life science and non-life science majors accepted (e.g. Biology, Chemistry, Psychology, Sociology, Communications, Marketing/Public Relations, etc.) -Ability to interface with peers and hospital personnel on assignments. -Excellent telephone and communication skills. -Ability to work in a dynamic environment (sometimes stressful, multi-tasking skills required etc.) -Position will require shift work on weekends, nights, and on holidays The incumbent should understand that the aforementioned job description only outlines certain requirements for this position. At the discretion of President/CEO or the CFAO, this job description may be amended as deemed necessary for the incumbent to render a more efficient and effective operation. \nCompany Description Georgia Eye Bank is IMPROVING VISION AND LIVES through transplantation of ocular tissue and cells, innovation, research, education, and collaboration to advance treatments and patient outcomes. Founded in 1961, Georgia Eye Bank is a 501(c)(3) nonprofit organization which is an accredited member of the Eye Bank Association of America and registered with the U.S. Food & Drug Administration. *Email communications from Georgia Eye Bank come from the georgiaeyebank.org email address. Scammers impersonate reputable companies, such as ours, and attempt to steal your identity. If you suspect fraud, please get in touch with the FTC or ZipRecruiter's fraud department at trustandsafety at ziprecruiter.com. Georgia Eye Bank is IMPROVING VISION AND LIVES through transplantation of ocular tissue and cells, innovation, research, education, and collaboration to advance treatments and patient outcomes. \n\nFounded in 1961, Georgia Eye Bank is a 501(c)(3) nonprofit organization which is an accredited member of the Eye Bank Association of America and registered with the U.S. Food & Drug Administration.\n\n*Email communications from Georgia Eye Bank come from the georgiaeyebank.org email address. Scammers impersonate reputable companies, such as ours, and attempt to steal your identity. If you suspect fraud, please get in touch with the FTC or ZipRecruiter's fraud department at trustandsafety at ziprecruiter.com.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves livesand we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to lifeimpacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potentialone discovery at a time. The Inside Sales Representative is a quota-carrying seller responsible for full-cycle sales of research grade products and manufacturing solutions, while feeding the GMP pipeline through qualified lead generation and supporting technical qualification and value selling of modality-based solutions for cell and gene therapy developers. This position reports to the Manager, Inside Sales and is part of the North American Sales Team located in Fargo, ND and will be a fully remote role. In this role, you will have the opportunity to: • Own full-cycle sales for research grade products and manufacturing solutions, from lead generation through deal closure, with disciplined funnel management, • Proactively engage and grow a portfolio of research-grade clients, driving order growth through value-based selling, • Identify, qualify, and transition GMP (clinical) leads to BDMs to build and accelerate the clinical pipeline, • Collaborate with technical sales to support technical qualification and deliver modality-based solutions for cell and gene therapy developers, • Partner with genomic medicine pioneers to solve complex drug development challenges and accelerate life-changing therapies The essential requirements of the job include: • Bachelor's degree in Life Sciences, Biology, Biotechnology, or a related field, • 2+ years of sales, technical or customer service experience in the life sciences, biotechnology, or a related technical industry, • Demonstrated ability to learn, understand, and communicate complex scientific or technical concepts Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role • Ability to travel 5-10% within territory or to company locations for client-facing or internal meetings It would be a plus if you also possess previous experience in: • CDMO, CMO or CRO services, • Cell and Gene Therapy or Vaccines, • Drug Development, • Using Customer Relationship Management (CRM) systems (e.g., HubSpot, Salesforce), • Selling or supporting research reagents, plasmid DNA, mRNA, or related life sciences products Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

The Opportunity: As a SAP Supply Chain Manager you will lead client service work focused on SAP supply chain and operations, helping clients optimize operational efficiency through application consulting, implementation, training, and support. As a Manager you will motivate and develop teams, guide workstreams, manage performance, and use technology and innovation to shape deliverables while leading with integrity and authenticity. In this role at PwC, you will help clients assess needs, implement SAP solutions, and support seamless adoption within our Digital Core Modernisation practice, drawing on work in Finance Technology - SAP Core ERP and the broader SAP competency to help organizations improve supply chain processes and advance strategic goals. Responsibilities: • Leading SAP supply chain and operations client workstreams from planning through delivery, • Managing project scope, budgets, schedules, and deliverables across multiple client engagements, • Analyzing supply chain processes to identify gaps in planning, procurement, inventory, and warehouse operations, • Developing and implementing SAP SCM solutions that improve process efficiency and operational visibility, • Coordinating requirements gathering, solution design, testing, and deployment activities for SAP initiatives, • Reviewing deliverables for accuracy, alignment to client needs, and consistency with firm methodologies, • Coaching team members on SAP supply chain processes, delivery approaches, and issue resolution, • Identifying opportunities to improve supply chain performance through data modeling, reporting, and process improvement, • Communicating progress, risks, and action items to clients and internal leadership throughout the project lifecycle, • Applying knowledge of supply chain management software, demand planning, procurement strategy, and warehouse management systems What You Must Have: • At least a Bachelor's degree, • At least 5 years of experience What Sets You Apart: • Preference for a Master's or Masters of Business Administration degree in at least one of the following fields of study: Biology/Biomedical Sciences, Business Administration/Management, Computer Science/Information Systems, Engineering, Health Administration/Public Health, Operations/Supply Chain, Science, • Demonstrating SAP Supply Chain transformation delivery for client accounts, • Leading project budgeting, planning, and execution across supply chain workstreams, • Mentoring teams through process improvement and operational excellence initiatives, • Translating supply chain analysis into data-driven insights for executives, • Applying SAP Supply Chain Management and warehouse management system knowledge Travel Requirements: Up to 80% The salary range for this position is: $99,000 - $232,000. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. All hired individuals are eligible for an annual discretionary bonus. PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation, personal and family sick leave, and more.

Job Type: Flexible Contract (Remote) Cobalt is hiring experienced biologists to review and build tasks that test whether frontier AI models can reason through real experimental science. Your job is to judge whether a model’s reasoning about an experiment is correct, and to explain precisely where it goes wrong when it is not. We are especially looking for scientists with hands-on flow cytometry experience. If you are the person in your lab who spots the flawed control, the mislabeled gate, or the conclusion the data does not support, this role is built around that skill. What you will do • Review AI-generated answers to experimental biology problems end to end, including the experimental design, the methods, the data interpretation, and the final conclusion, and confirm that each step is scientifically sound and consistent with the others., • Write realistic problems from your own area of expertise, along with reference solutions that show the reasoning a skilled scientist would follow, not only the final answer., • Look for ways a model could reach a correct-looking answer without sound reasoning, such as relying on a textbook pattern that does not fit the data, ignoring a missing control, or overlooking an artifact, and document each issue clearly., • Judge whether a model’s failure reflects a real gap in scientific reasoning, or instead reflects an ambiguous question, missing information, or an unfair reference answer., • Write clear, specific feedback and work with task authors through revisions until each task meets the acceptance standard., • Join occasional expert calls of 30 to 60 minutes with research teams who want to understand how experts approach a specific problem. Example tasks you might review include designing a multicolor flow cytometry panel for a given set of markers and instrument, critiquing a gating strategy and identifying where a population was misassigned, explaining why compensation errors produced a false double-positive population, and judging whether a reported difference between treatment groups is supported by the data. Who we are looking for • PhD in biology, immunology, cell biology, biochemistry, or a closely related life sciences field., • Hands-on laboratory experience, gained through research, a thesis, a postdoctoral position, a core facility, or industry work. You should be comfortable reading an experimental protocol and saying whether it would work., • Strong working knowledge of experimental design, including controls, replicates, and when a difference between two results is meaningful., • Careful, direct written communication. Much of the job is explaining precisely what is wrong and why., • No prior experience with AI is required. Strong advantages • Hands-on flow cytometry experience, including panel design, compensation, gating, and data analysis, using instruments such as the BD FACSymphony or Cytek Aurora and software such as FlowJo, FCS Express, or OMIQ., • Experience with spectral or mass cytometry, or with clinical flow cytometry such as leukemia and lymphoma immunophenotyping., • Experience managing or working in a core facility, training other scientists, or serving as a peer reviewer for a journal. Why Cobalt AI • Shape how AI understands science. Your judgment directly determines which tasks are used to measure what leading models can and cannot do in biology., • Use your expertise in a new way. You will see up close how frontier models reason about experiments and where they break., • Fit the work around your current role. Set your own schedule, with flexible weeks that can scale up or down around your research and other commitments., • Grow with us. Strong reviewers can move into task design, project leadership, and research collaborations on future projects.

InnoCare (HKEX: 09969; SSE: 688428) is a commercial stage biopharmaceutical company committed to discovering, developing, and commercializing innovative drugs for the treatment of cancers and autoimmune disease, with unmet medical needs worldwide. InnoCare has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization. To date, the Company has developed a robust product pipeline comprising three approved drugs (orelabrutinib, tafasitamab and zurletrectinib), and more than ten innovative drug candidates in clinical development, and multiple programs in preclinical stages. InnoCare has successfully got listed on both Hong Kong Stock Exchange and the STAR Board of Shanghai Stoch Exchange. Our world-class team exhibits remarkable synergy and efficient execution, with entrepreneurial spirit, which has made outstanding achievements in innovation, commercialization and globalization. If you would like to join us, we will develop innovative drugs for the benefit of patients worldwide. Website link: https://www.innocarepharma.com/en. LinkedIn: InnoCare Pharma. Key Responsibilties Project Leadership • Lead discovery projects, formulate medicinal chemistry strategies, engage in compound design and SAR analysis. Team Management • Manage and motivate a medicinal chemistry team, provide professional guidance to team members, help resolve technical difficulty. Cross-function collaboration • Closely work with computational chemistry, biology, pharmacology and DMPK functional groups. Requirements • PhD degree in Organic Chemistry with over seven years of working experience in the pharmaceutical industry., • An expert in medicinal chemistry, ligand- and structure-based drug design., • Proven track record of leading discovery programs to the clinical stage., • Excellent communication and problem-solving skills.

STEM Expert (MSc./PhD) (Remote | $60–$120/hr) Position: STEM Expert (MSc./PhD) Type: Contractor (Part-Time, approximately 15 hours/week) Compensation: $60–$120/hour Location: Remote (Worldwide) About the Opportunity This opportunity is for STEM and scientific-domain experts to contribute to AI training through technical problem-solving, scientific reasoning, data analysis, and Python-based workflows. Candidates need deep expertise in at least one relevant scientific or quantitative field; expertise across all STEM disciplines is not required. Key Responsibilities • Solve complex scientific, mathematical, and technical problems within your area of expertise., • Review AI-generated solutions for scientific, mathematical, and factual accuracy., • Identify incorrect assumptions, reasoning errors, and overlooked constraints., • Use Python or other programming languages for calculations, simulations, and validation., • Provide rigorous, technically accurate solutions and feedback. Required Qualifications • Strong expertise in at least one STEM field, such as chemistry, biology, mathematics, physics, geoscience, environmental science, or robotics., • Practical proficiency in Python or another programming language., • Strong scientific, mathematical, or quantitative problem-solving skills., • Experience using coding agents in technical workflows. Preferred Qualifications • Familiarity with scientific tools such as NumPy, SciPy, pandas, SymPy, Jupyter, or relevant domain-specific libraries., • Relevant expertise gained through academic research, industry, teaching, engineering, or independent technical work. Compensation • $60–$120/hour, with output-based payment for tasks meeting project specifications., • Approximately 15 hours per week with a flexible schedule., • Immediate availability preferred; first task expected within 24–48 hours after onboarding. Application Process • Apply for the role and complete the screening questions., • Complete an AI interview of approximately 30 minutes., • Complete the hiring manager review., • If selected, complete onboarding and begin the first task within 24–48 hours.

PhD in Marine Biology, Ecology, Environmental Science, or a related field – candidates without a PhD will not be considered for this role;.

Perimeter College invites applications for a tenure-track assistant professor position in Biology. Assistant Professor of Biology. One year is preferred and can include experience as a teaching assistant at a college or university.

The Perimeter College Department of Life and Earth Sciences includes a wide-ranging community of students, staff members and distinguished faculty scholars in the fields of biology, environmental science, geology and integrated sciences. Others pursue non-science educational goals and careers. Part-

Georgia Institute of Technology (Georgia Tech) in Atlanta, Georgia, invites applications for a tenure-track faculty position in Mathematical Biology to start in August 2027.

Graduate degree programs include: MS and PhD in Biology, MS and PhD in Bioinformatics, MS and PhD in Computational Science and Engineering as well as PhD in Quantitative Biosciences, Ocean Sciences and Engineering, Applied Physiology, and Dual Degree Doctor of Physical Therapy/ Doctor of Philosophy.

STEM Expert (MSc./PhD) (Remote | $60–$120/hr) Position: STEM Expert (MSc./PhD) Type: Contractor (Part-Time, approximately 15 hours/week) Compensation: $60–$120/hour Location: Remote (Worldwide) About the Opportunity This opportunity is for STEM and scientific-domain experts to contribute to AI training through technical problem-solving, scientific reasoning, data analysis, and Python-based workflows. Candidates need deep expertise in at least one relevant scientific or quantitative field; expertise across all STEM disciplines is not required. Key Responsibilities • Solve complex scientific, mathematical, and technical problems within your area of expertise., • Review AI-generated solutions for scientific, mathematical, and factual accuracy., • Identify incorrect assumptions, reasoning errors, and overlooked constraints., • Use Python or other programming languages for calculations, simulations, and validation., • Provide rigorous, technically accurate solutions and feedback. Required Qualifications • Strong expertise in at least one STEM field, such as chemistry, biology, mathematics, physics, geoscience, environmental science, or robotics., • Practical proficiency in Python or another programming language., • Strong scientific, mathematical, or quantitative problem-solving skills., • Experience using coding agents in technical workflows. Preferred Qualifications • Familiarity with scientific tools such as NumPy, SciPy, pandas, SymPy, Jupyter, or relevant domain-specific libraries., • Relevant expertise gained through academic research, industry, teaching, engineering, or independent technical work. Compensation • $60–$120/hour, with output-based payment for tasks meeting project specifications., • Approximately 15 hours per week with a flexible schedule., • Immediate availability preferred; first task expected within 24–48 hours after onboarding. Application Process • Apply for the role and complete the screening questions., • Complete an AI interview of approximately 30 minutes., • Complete the hiring manager review., • If selected, complete onboarding and begin the first task within 24–48 hours.

Under the direction of section supervisors, this position plays leadership role in the execution and management of animal training, care, handling, and performance of pinnipeds utilized for Georgia Aquarium's pinniped show and other programs as applicable. Primary objectives and responsibilities are to assist the management team with the development and implementation of daily shows, guest interaction programs, environmental enrichment programs, and staff development. Participates in daily show performances and animal sessions to facilitate public programming with pinnipeds. Executes daily routine operations in accordance with section's standard operating procedures. Mentors junior staff in their respective job responsibilities. Responsibilities include: • Assists the management team in overseeing all aspects of daily care and behavioral conditioning of pinnipeds., • Under direction of section supervisors, coordinates the execution of daily and long-term animal training goals, including enrichment, new learning, show quality, and staff development., • Assists section supervisors with the development and implementation of dynamic animal training projects and programs that serve to enhance animal care, animal management, guest experience, and Aquarium public relations., • Ensures the daily health, care, and welfare of the pinniped collection., • Trains pinniped collection in accordance with Georgia Aquarium's animal training protocols. Actively participates in the progression of animal training goals and standards. Develops behavior to facilitate show performances, public programs, animal management and care., • Mentors junior staff on animal training, show performance, animal care, environmental enrichment, animal handling and general aquarium operations. Oversees and facilitates the developmental goals of volunteers, interns, Apprentice Trainers, Assistant Trainers, and Trainers., • Executes daily pinniped show performances. Maintains a superior level of showmanship while performing primary/key roles in daily shows., • Interacts with guests and crew members in a positive and professional manner., • Facilitates and maintains comprehensive pinniped environmental enrichment program. Mentors junior staff on the development of novel environmental enrichment devices and activities., • Coordinates with management to orchestrate the casting of trainer/animal roles for daily shows, guest interaction programs, and other special events and programs as appropriate., • Performs the execution of complex behaviors as integral part of Georgia Aquarium's pinniped show., • Follows established standard operating procedures for animal care, food preparation, and clean up, including proper maintenance and sterilization of equipment. Assists in maintaining the highest standards in area cleanliness, diet preparation, record keeping, and animal observations., • Ensures pinniped facilities are maintained in compliance with industry and government standards in the areas of cleanliness/sanitation, diet preparation, record keeping and general maintenance., • Assists management team in coordination of animal handling for medical care and transport., • Assists management and maintenance of records management systems for animal inventory, care, training, and enrichment., • Inputs data and information into records management systems for animal inventory, care, training, and enrichment., • Executes underwater maintenance and cleaning of habitats., • Maintains SCUBA certification. Functions as a diver, dive tender, standby diver (TSBD), and designated person in charge (DPIC) during underwater activities carried out by Georgia Aquarium., • Follows dive safety guidelines established by the dive safety officer., • Fosters good relations with visitors, volunteers, community leaders, contractors, and fellow staff members by promoting positive attitudes, good will, cooperation, and providing high standards of service., • Complies with all Georgia Aquarium policies, procedures, and programs., • As needed, interact on behalf of the Georgia Aquarium with guests, media, general public, etc., • To perform other duties as workload necessitates, regardless of time of day or location. Qualifications include: • Four-year degree in biology or related field; equivalent relevant experience may be considered in lieu of a four-year degree at the discretion GAI., • Minimum four years of aquatic animal husbandry and training working with marine mammals, experience in an AZA/AMMPA accredited institution, or equivalent, with a proven track record of team oriented and professional performance., • Extensive background in animal training., • Experience in show performance and public programs preferred., • Working knowledge of life support operation and water quality control for maintaining marine mammals., • Strong team skills., • Strong oral and written communication skills., • Valid State of Georgia driver's license, or the ability to obtain one., • Valid passport, or the ability to obtain one., • Proficiency with Personal Computer (P.C.) hardware and contemporary software including Microsoft Office Products., • SCUBA certification., • Ability to pass departmental swim test, which includes, but is not limited to minimum requirements for treading water, breath holding, free diving and endurance. Physical Demands & Work Environment include: The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; climb stairs; balance; stoop, kneel, crouch or crawl; talk or hear; taste or smell. The employee must occasionally lift and/or move up to 50 pounds 100 feet. Specific vision abilities required by the job include close vision, distance vision, color and peripheral vision, depth perception, and the ability to adjust focus. While performing the duties of this job, the employee is exposed to weather conditions prevalent at the time. Elements of the position require employees to wear a wet suit for extended periods throughout the day. This position requires direct contact with raw seafood. The noise level in the work environment is usually moderate. An employee must also have the ability to travel by car, boat and air as needed, physically use SCUBA equipment, conduct field work in the collection and research of animals, and maintain daily contact with a living collection of plants and animals. Commitment to Georgia Aquarium, Inc. includes: Mission: Georgia Aquarium is a nonprofit committed to inspiring awareness and preservation of our ocean and Aquatic animals worldwide. Vision: To be the Premier Aquarium in the World for Science, Entertainment, Education and Conservation. Values: Respect, Teamwork, Integrity, Innovation, Leadership, Excellence, Appreciation & Inclusion Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

At Confluent Health and our family of affiliated brands, our PT Technicians are an important part of the patient experience. You'll work side by side with licensed physical therapists, help patients feel welcomed and supported, and play a key role in keeping the clinic running smoothly. This is a fast-paced, hands-on role with direct patient interaction and plenty of opportunity to learn. Whether you're looking to grow as a PT Technician or gain experience as you pursue a future in physical therapy or healthcare, you'll be part of a team where your contribution matters. What We Offer • Health, dental, and vision insurance (eligibility varies by schedule), • Paid time off, • Family building and parental leave benefits, • 401(k) with employer match up to 4%, • Hands-on training and experience working alongside licensed physical therapists, • Nationwide growth opportunities across our family of brands, • Mentorship, professional connections, and opportunities for recommendation letters that can support PT, PT A, and other healthcare school applications, • Scheduling options that may work around school or other commitments, • A team culture built around taking exceptional care of patients, working hard, and having fun together Responsibilities • Greet patients and bring them to treatment areas, ensuring they have a staff member with them, • Guide patients through exercise programs as directed by the treating therapist, • Set up and take down modalities such as heat, ice, e-stim, Game Ready, and Normatec as directed by the therapist, • Clean and sanitize treatment tables, equipment, and rooms between patients, • Keep the clinic stocked and organized, including laundry and restocking supplies, • Anticipate the needs of therapists and patients and assist where needed, • Support the front desk and other members of the clinic team during downtime, • Protect patient privacy and uphold HIPAA standards in every interaction Qualifications • High school diploma or GED, • Strong communication and customer service skills, with the ability to interact effectively with patients of all ages, including those who may be experiencing pain or discomfort, • Ability to follow direction from licensed therapists and carry out assigned patient support activities, • Ability to manage multiple tasks and priorities in a fast-paced clinic environment, • Ability to work collaboratively with therapists, front office staff, and other members of the clinic team, • Ability to take initiative and identify clinic, patient, and team needs within the scope of the role, • Ability to remain on your feet throughout your shift and perform routine clinic activities including cleaning, laundry, restocking supplies, and moving equipment, • Ability to maintain patient privacy and follow HIPAA and clinic standards, • Reliable attendance and the ability to commit to a consistent work schedule; daytime availability is preferred Preferred • Currently pursuing or have completed a degree in kinesiology, exercise science, health science, biology, or a related pre-PT field preferred, • Previous experience in customer service, fitness, personal training, coaching, sports, or another patient- or customer-facing environment preferred Compensation: $15.00/hr Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse and inclusive workforce. We do not discriminate based on race, color, religion, sex, sexual orientation, gender (including pregnancy, childbirth, or related medical conditions), gender identity or expression, national origin, marital status, age, disability, veteran status, or other applicable legally protected characteristics. If you need assistance or would like to request an accommodation due to a disability, please contact us at careers@goconfluent.com.

With five decades of experience, Shepherd Center provides world-class clinical care, research, and family support for people experiencing the most complex conditions, including spinal cord and brain injuries, multi-trauma, traumatic amputations, stroke, multiple sclerosis, and pain. An elite center ranked by U.S. News as one of the nation's top hospitals for rehabilitation, Shepherd Center is also recognized as both Spinal Cord Injury and Traumatic Brain Injury Model Systems. Shepherd is the only rehabilitation facility in the nation with an intensive care unit on-site, allowing us to care for the most complex patients and begin the rehabilitation process sooner. Shepherd Center treats thousands of patients annually with unmatched expertise and unwavering compassion to help them begin again. Shepherd Center's culture is one of hope, humor, and hard work. You will enjoy career growth, strong relationships with co-workers, strong support from leadership, and fun activities that have kept over 12% of staff members working at Shepherd for more than 20 years. The PT and OT Aide assists the Physical and Occupational Therapists to prepare the environment and the patient for routine care and assists the patient with routine activities of daily living as determined in treatment plan. All activities are performed under the direct supervision of a licensed OTR, PT, COTA, or PTA. This hands-on role contributes to the improvement of patient experience through rehabilitation services. This collaborative role addresses and resolves issues in order to facilitate patient recovery. Job Responsibilities: • The PT and OT Aide assists in creating a welcoming environment for patient care., • Transports patients throughout the center., • Assembles equipment and adjusting it to patient needs., • Assists patients with transfers on the nursing units, in preparation for a PT session, or as directed., • Assists patient with weight shifts and other daily activities (grooming, feeding, dressing, toileting, bathing etc.) or assigned OT therapy activities., • Conducts assigned OT groups or assisting PTs or PTAs in a group setting., • Maintains the therapy and nursing equipment and environment., • Cleans and returns wheelchairs, bathroom equipment, and other equipment as assigned., • Completes assigned clerical duties., • Instructs new employees and volunteers in departmental maintenance tasks., • Attends and actively contributes to department meetings., • Performs consistent with Shepherd Center standards, clinical policies, and procedures., • Practices proper safety techniques in accordance with Center and departmental policies and procedures. Responsible for the reporting of employee/patient/visitor injuries or accidents, or other safety issues to the supervisor and in the occurrence notification system., • Monitors and ensures compliance with all regulatory requirements, organizational standards, and policies and procedures related to area of responsibility. Identifies potential risk areas within area of responsibility and supports problem resolution process., • Performs other duties as required/requested/assigned. Required Minimum Education • High School Diploma or equivalent Required Minimum Certification • No minimum certification Required Minimum Experience • Previous therapy aide or clinical/healthcare experience preferred. Required Minimum Skills • Basic computer skills., • This is a support role that requires an individual to be able to interact directly with patients in a positive and supportive manner., • Ability to learn and operate therapy equipment., • Must display knowledge of growth, development and the ability to obtain, interpret and disseminate information in terms of age specific patient needs (adolescent, adult and geriatric., • Ability to follow instructions and problem solve., • Takes responsibility for growing professionally and seek opportunities for improving skills., • Communicates effectively using timely verbal, non-verbal and written communication., • Willingly adapts to changing work demands and work environment., • Demonstrates critical thinking skills and makes sound judgments to monitor and respond to patient needs or changes in condition., • Completes orientation and initial assessment of competency successfully by determined due date., • Completes mandatory education and annual competency assessment requirements by determined due date. Preferred Qualifications • A bachelor's degree in exercise science, health science, biology or related field of study preferred., • Previous experience with patients with Spinal Cord Injury, Traumatic Brain Injury Stroke, Concussion and Vestibular Disorders. Physical Demands • Uses body, tools, or special devices to safely, effectively, and efficiently to move, guide, or place patients. Involves some latitude for judgement with regard to precision attained and the selection of what adaptive device(s) to utilize., • Ability to transfer and position patients, consistent with lifting up to 30 lbs., • Repetitive lifting, moving, squatting, kneeling, and crawling physical requirements. Working Conditions • Normal patient care environment., • Some potential for exposure to blood and body fluids., • Some potential exposure to infectious viruses. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be an exhaustive list of all job duties performed by the personnel so classified.

At Confluent Health and our family of affiliated brands, our PT Technicians are an important part of the patient experience. You'll work side by side with licensed physical therapists, help patients feel welcomed and supported, and play a key role in keeping the clinic running smoothly. This is a fast-paced, hands-on role with direct patient interaction and plenty of opportunity to learn. Whether you're looking to grow as a PT Technician or gain experience as you pursue a future in physical therapy or healthcare, you'll be part of a team where your contribution matters. What We Offer • Health, dental, and vision insurance (eligibility varies by schedule), • Paid time off, • Family building and parental leave benefits, • 401(k) with employer match up to 4%, • Hands-on training and experience working alongside licensed physical therapists, • Nationwide growth opportunities across our family of brands, • Mentorship, professional connections, and opportunities for recommendation letters that can support PT, PT A, and other healthcare school applications, • Scheduling options that may work around school or other commitments, • A team culture built around taking exceptional care of patients, working hard, and having fun together Responsibilities • Greet patients and bring them to treatment areas, ensuring they have a staff member with them, • Guide patients through exercise programs as directed by the treating therapist, • Set up and take down modalities such as heat, ice, e-stim, Game Ready, and Normatec as directed by the therapist, • Clean and sanitize treatment tables, equipment, and rooms between patients, • Keep the clinic stocked and organized, including laundry and restocking supplies, • Anticipate the needs of therapists and patients and assist where needed, • Support the front desk and other members of the clinic team during downtime, • Protect patient privacy and uphold HIPAA standards in every interaction Qualifications • High school diploma or GED, • Strong communication and customer service skills, with the ability to interact effectively with patients of all ages, including those who may be experiencing pain or discomfort, • Ability to follow direction from licensed therapists and carry out assigned patient support activities, • Ability to manage multiple tasks and priorities in a fast-paced clinic environment, • Ability to work collaboratively with therapists, front office staff, and other members of the clinic team, • Ability to take initiative and identify clinic, patient, and team needs within the scope of the role, • Ability to remain on your feet throughout your shift and perform routine clinic activities including cleaning, laundry, restocking supplies, and moving equipment, • Ability to maintain patient privacy and follow HIPAA and clinic standards, • Reliable attendance and the ability to commit to a consistent work schedule; daytime availability is preferred Preferred • Currently pursuing or have completed a degree in kinesiology, exercise science, health science, biology, or a related pre-PT field preferred, • Previous experience in customer service, fitness, personal training, coaching, sports, or another patient- or customer-facing environment preferred We provide training on clinic workflows, modalities, cleaning standards, and patient care support. Compensation: $15.00/hr Full-time Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse and inclusive workforce. We do not discriminate based on race, color, religion, sex, sexual orientation, gender (including pregnancy, childbirth, or related medical conditions), gender identity or expression, national origin, marital status, age, disability, veteran status, or other applicable legally protected characteristics. If you need assistance or would like to request an accommodation due to a disability, please contact us at careers@goconfluent.com.

1. Job Purpose: • This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations;, • The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. 1. Responsibilities: • Planning of project activities and study timelines based on project goal and sponsor's expectation;, • Organize and Lead meeting/teleconferences for study activities implementation (e.g. investigator meeting, project review meeting etc), monitoring the progress of each CRA responsible sites, and assessing overall status of the project;, • Develop the project management plan, monitoring plan etc as required for the study;, • Develop study specific tools/forms, study templates as required for the study;, • Develop and manage project budget;, • Order and ensure all clinical supplies (including drug and non-drug) are adequate for all sites throughout the study period;, • Ensure all team members have timely access to appropriate systems and tools, if applicable (e.g. IVRS, eCRF etc);, • Organize and conduct site feasibility visits according to guidelines and make recommendation for final approval;, • Track study progress and ensure project is conducted according to the plan;, • Communicate to monitors new study information, study timelines and goals, study requirements. Responsible for raising overall project specific issues to management (e.g. Project Director, Senior Management);, • Submit the weekly project report to management (e.g. Project Director, Senior Management);, • Study site selection, initiation (SIV) and clinical monitoring;, • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience;, • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations;, • Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol, and requirements;, • Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files;, • Finalize budget and obtain signed contract from site, prior to site initiation visit;, • Provide guidance and training to entry-level CRA/CRA I/CRA II in collaboration with Line Manager. 1. Qualifications: • Bachelor degree or above in Medical, Pharmacology or Biology related major;, • Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;, • At least 1-3 years of Oncology CRA experience;, • Good command of written and verbal English;, • Good skills on Microsoft Word, Excel, PPT and Outlook, etc.;, • Other abilities such as Communication skills/Information-gathering skills. Knowledge and/or experience in medical practice is a plus. Welcome passion and creative ideas' friends! Look forward to receiving your profiles.