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Position Summary We are seeking a detail-oriented Validation Specialist to support validation and qualification activities within a pharmaceutical manufacturing environment. This individual will help ensure that manufacturing equipment, utilities, facilities, computerized systems, and processes are qualified and validated in accordance with applicable regulatory requirements, Good Manufacturing Practices (GMP), and company quality standards. The Validation Specialist will work cross-functionally with Quality Assurance, Engineering, Manufacturing, Quality Control, and other technical teams to develop and execute validation protocols, review documentation, investigate discrepancies, and maintain the validated state of manufacturing systems and processes. The ideal candidate has experience in pharmaceutical or biotechnology manufacturing, a strong understanding of validation principles, and the ability to manage documentation and projects in a regulated environment. Key Responsibilities Validation & Qualification • Develop, review, and execute validation and qualification protocols, reports, and supporting documentation., • Support equipment, facility, utility, and manufacturing process qualification activities., • Assist with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities., • Support process validation, cleaning validation, and sterilization validation, as applicable., • Participate in commissioning, qualification, and validation (CQV) activities for new or modified equipment and systems., • Ensure validation activities are completed according to approved procedures, project timelines, and regulatory expectations., • Maintain the validated state of equipment, systems, and processes through periodic reviews and requalification activities. GMP Compliance & Documentation • Ensure validation documentation complies with applicable GMP requirements, company procedures, and regulatory expectations., • Prepare, review, and maintain protocols, test scripts, technical reports, and validation summary reports., • Ensure validation records are accurate, complete, traceable, and inspection-ready., • Support change control activities and assess the impact of equipment, process, facility, and system changes on the validated state., • Assist with deviations, investigations, corrective and preventive actions (CAPA), and remediation activities related to validation., • Support internal audits, regulatory inspections, and quality system reviews as needed. Cross-Functional Collaboration • Partner with Quality Assurance, Engineering, Manufacturing, Quality Control, and Facilities teams to support validation projects., • Coordinate validation execution activities, including testing, data collection, documentation, and issue resolution., • Communicate project status, risks, discrepancies, and schedule impacts to relevant stakeholders., • Provide technical support and guidance regarding validation requirements and documentation practices. Continuous Improvement • Identify opportunities to improve validation processes, documentation practices, and project execution., • Support risk assessments and validation strategies using a science- and risk-based approach., • Assist with the development and maintenance of validation plans, procedures, and standard operating procedures (SOPs)., • Support the implementation of industry best practices and evolving regulatory expectations. Required Qualifications • Bachelor's degree in Engineering, Chemistry, Biology, Pharmaceutical Sciences, or a related scientific or technical discipline preferred; equivalent relevant experience may be considered., • Typically 2–5 years of experience in validation, qualification, quality assurance, engineering, or a related function within pharmaceutical, biotechnology, or regulated manufacturing., • Working knowledge of GMP requirements and pharmaceutical manufacturing practices., • Experience preparing, executing, or reviewing validation protocols and reports., • Familiarity with IQ, OQ, and PQ documentation and execution., • Strong technical writing, documentation, organizational, and problem-solving skills., • Ability to manage multiple priorities and collaborate effectively with cross-functional teams., • Proficiency with Microsoft Office and electronic quality or document management systems.

Quality Investigator (Contract) Location: Raleigh, NC Pay: $40–$50/hour Employment Type: Contract (Open-ended with potential to convert to a full-time position) We are seeking a Quality Investigator to join a growing Quality Assurance team supporting a regulated manufacturing environment. This individual contributor role partners cross-functionally with Manufacturing, Quality, Engineering, and Supply Chain to investigate quality events, drive compliance initiatives, and support continuous improvement efforts. Key Responsibilities • Conduct investigations for quality events, deviations, and exceptions, including root cause analysis and CAPA recommendations., • Perform Phase II Out-of-Specification (OOS) investigations., • Support internal and external regulatory audits by preparing documentation and assisting audit activities., • Analyze quality metrics and trends, including KPI reporting and data analysis., • Assist with Annual Product Reviews (APRs) and quality management reporting., • Revise and maintain SOPs and quality documentation as needed., • Participate in continuous improvement initiatives, Kaizen events, and GEMBA walks., • Track investigation progress and communicate status updates to leadership., • Ensure compliance with GMPs, SOPs, and applicable regulatory requirements., • Utilize SAP and other quality systems to support documentation and reporting. Qualifications • Bachelor's degree in Chemistry, Biology, Microbiology, Engineering, or another scientific discipline preferred (relevant experience may be considered in lieu of a degree)., • 3–5 years of experience in a pharmaceutical, biologics, medical device, or other FDA-regulated manufacturing environment., • Experience conducting investigations, root cause analysis, CAPA development, and quality documentation., • Knowledge of GMP regulations and quality systems., • Proficiency with Microsoft Office; SAP experience is a plus., • Strong written and verbal communication skills with excellent attention to detail and organizational skills. Work Environment • Monday–Friday, onsite in Raleigh, NC., • Office-based with regular interaction in manufacturing, laboratory, warehouse, and cleanroom environments., • Must be able to wear required PPE and occasionally lift up to 40 lbs., • Occasional weekend work may be required based on business needs. This is an excellent opportunity for a quality professional looking to gain experience with a leading regulated manufacturer. While this is a contract position, there is no defined end date, and the role offers the potential to convert to a full-time opportunity based on business needs and performance.

Job Description Xylem Tree Care is hiring Climbers for our Residential/Commercial crew in Raleigh, NC. The Climber is responsible for climbing, pruning, and removing trees. Previous professional experience as a climber is required to be considered for this role. ESSENTIAL FUNCTIONS • Perform tree climbing using rope and saddle techniques in accordance with industry standards, • Prune and remove trees safely and efficiently, • Operate chainsaws, rigging equipment, and other tree care tools, • Assist with job site setup, traffic control, and cleanup, • Follow all safety procedures and company policies, • Communicate effectively with crew members and supervisors, • Maintain equipment and report any issues SUPERVISORY RESPONSIBILITIES • Climbers have no direct reports. EXPERIENCE REQUIREMENTS • Minimum of two (2) years of professional tree climbing experience (Required), • CDL (Preferred but not required) EDUCATION REQUIREMENTS • High School diploma or education equivalent preferred KNOWLEDGE, SKILLS, AND ABILITIES • Self-motivated, with great attention to detail and a strong work ethic, taking pride in delivering high-quality tree work, • Knowledge of proper pruning techniques and tree biology, • Proven experience as a tree climber with a strong understanding of basic climbing and rigging techniques, including knowledge of knots and roping procedures, • Ability to safely operate chainsaws and climbing equipment, • Strong understanding of safety standards (ANSI Z133 preferred), • Must be able to work outdoors, year-round, in varying environments, • Must have a Valid driver’s license Work authorization requirements: Must meet I-9 requirements. Affirmative Action/EEO statement: Xylem Tree Experts and Kendall Vegetation Services provide equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this job. Duties, obligations, and activities may change at any time, with or without notice. Reasonable Accommodation Statement XKIG is an equal opportunity employer and complies with all federal, state, and local nondiscrimination laws, including the ADA. If you need a reasonable accommodation during the application or hiring process, please contact our Talent Acquisition team at 877-418-2999. Benefits Offered: This is a full-time position that offers health insurance benefits for medical, vision, and dental, as well as the option for enrollment in a 401K. Paid Time Off (PTO) Eligibility and accrual timelines vary by position with some roles gaining PTO immediately and others becoming eligible after a set period of employment. Details are provided during the hiring process and may vary for Union hires. AI Usage Disclaimer: As part of our commitment to efficiency and innovation, we may use artificial intelligence (AI) tools during the recruiting and onboarding processes. These tools assist with tasks such as resume screening, interview scheduling, and communication. All decisions regarding hiring and employment are ultimately made by our human team. If you have questions or concerns about this process, please contact our HR department.

Job DescriptionDescription: Alliance Biotech Solutions is seeking a dedicated QC Microbiologist to support Environmental Monitoring (EM) and microbiological testing activities within a GMP manufacturing environment. This role is responsible for performing routine environmental monitoring in controlled manufacturing areas and executing microbiological testing within the QC laboratory. The ideal candidate will have hands-on experience collecting environmental samples in cleanroom environments and performing laboratory testing such as bioburden and endotoxin analysis. This position requires a strong understanding of aseptic techniques, GMP documentation practices, and microbiological testing methodologies. Requirements: • Perform environmental monitoring activities collecting samples including non-viable particulates, viable air, surface, clean gas, and clean utilities., • Collect environmental samples within ISO classified manufacturing areas while adhering to GMP and aseptic practices., • Transport, document, and process environmental monitoring samples in accordance with approved procedures., • Perform routine microbiological testing including bioburden, endotoxin, and other QC microbiology assays as required., • Prepare media, reagents, and laboratory materials necessary for environmental monitoring and microbiological testing activities., • Incubate, read, enumerate, and document microbiological test results and environmental monitoring data. -Support investigations related to environmental monitoring excursions, out-of-specification results, deviations, and contamination control activities. • Maintain laboratory and monitoring equipment, complete GMP documentation, and support cleanroom qualification and utility monitoring programs. Experience/Skills • Bachelor’s degree in Microbiology, Biology, Biotechnology, or a related life sciences field., • 3+ years of QC Microbiology experience in a pharmaceutical or biotech GMP environment., • Hands-on experience performing Environmental Monitoring activities, including viable air, surface, personnel, non-viable particulate, gas, and clean steam sampling., • Experience performing microbiological testing such as bioburden, endotoxin, microbial enumeration, and related QC lab assays., • Comfortable working independently in cleanroom environments for extended periods., • Knowledge of GMP, GLP, and aseptic processing practices., • Comfort using LIMS systems, • Ability to work in classified cleanroom areas, follow aseptic techniques, and perform routine monitoring activities. Benefits & Compensation • Industry competitive wage as a full-time employee, • Flexible Paid Time Off, • Medical, Dental and Vision Insurance with low employee cost, • Employer paid long term and short-term disability, • 401k plan with employer contributions About Alliance Biotech Solutions Alliance Biotech Solutions (ABS) is a premier consulting firm specializing in biopharmaceutical engineering and validation services. As industry leaders in Commissioning, Qualification, and Validation (CQV), we provide crucial services to the biotech and pharmaceutical sectors while maintaining our philosophy that employees are our #1 priority. Our success is built on the foundation of empowering our team members' growth and development, recognizing that our employees are the cornerstone of our clients' success. Alliance Biotech Solutions is an Equal Employment Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, citizenship status, military status, protected veteran status, religion, creed, physical or mental disability, medical condition, marital status, sex, sexual orientation, gender, gender identity or expression, age, genetic information, or any other basis protected by law, ordinance, or regulation. Alliance Biotech Solutions does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Alliance Biotech Solutions, and Alliance Biotech Solutions will not be obligated to pay a placement fee. All persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Job DescriptionCompany Description Lochner and Egis are entering an exciting new chapter as one organization. We have combined decades of trusted U.S. engineering expertise with the global reach, technical excellence, and career opportunities of a leading international engineering, consulting, and infrastructure firm. While our name has changed, our commitment to our people, clients, and communities is stronger than ever. At Egis, every project is an opportunity to create lasting impact. We collaborate with public and private clients to design and deliver innovative transportation, aviation, rail, transit, water, structural, environmental, and infrastructure solutions that connect communities and improve everyday life. Join a team where innovation is encouraged, collaboration is valued, and your work helps build a more sustainable future. Job Description The Impact You'll Make • Conduct natural resources field investigations including wetland delineations, stream assessments, habitat evaluations, protected species surveys, and environmental site assessments., • Perform environmental field work and collect data in support of transportation and infrastructure projects throughout North Carolina., • Prepare natural resources technical reports (NRTRs), environmental permitting packages and coordinate with regulatory agencies to support project approvals., • Perform on-site natural resources field investigations and/or inspections and collect samples of soil, water, air, and biological materials to assess environmental conditions and identify potential environmental impacts., • Utilize GIS and other software tools to develop mapping, environmental exhibits, and project documentation., • Support transportation planning and design teams by identifying environmental constraints and recommending avoidance, minimization, and mitigation strategies., • Assist with the development of NEPA/SEPA documentation, environmental studies, technical reports, and project deliverables., • Participate in public involvement efforts, agency coordination, and stakeholder meetings as needed., • Collaborate with multidisciplinary project teams to deliver high-quality environmental solutions that meet project schedules and client objectives.Qualifications The Expertise You'll Bring • Bachelor's degree in Environmental Science, Biology, Ecology, Natural Resources, Geography, or a related field., • 5+ years of experience in environmental permitting, environmental planning, and transportation-related projects., • Experience preparing environmental documentation and permitting packages for transportation and infrastructure projects., • Working knowledge of NEPA and SEPA processes and environmental compliance requirements., • Experience working with NCDOT, resource agencies, local governments, or related transportation clients preferred., • Proficiency with GIS and Microsoft Office applications; MicroStation or CADD experience is a plus., • Strong technical writing, communication, and analytical skills., • Ability to manage multiple assignments while working independently and collaboratively within a team environment., • Self-starter with strong organizational, research, and problem-solving abilities., • Ability and willingness to travel to project sites and occasionally stay overnight when required. Additional Information Why You'll Thrive at Egis At Egis, you'll do more than build your career—you'll help shape the future of infrastructure. As we continue to expand across the United States, we're looking for curious, collaborative professionals who are passionate about solving complex challenges and delivering projects that improve communities and create lasting impact. Whether you're launching your career or bringing years of experience, you'll have the opportunity to work alongside industry-leading experts, collaborate across disciplines and borders, and contribute to projects that transform the way people live, move, and connect. Here, you'll be empowered to take on meaningful work, develop new skills, and grow your career with the support of a global engineering leader. What Sets Egis Apart • Meaningful Projects – Contribute to complex infrastructure projects that strengthen communities and improve quality of life., • Global Expertise, Local Impact – Collaborate with technical specialists across North America and around the world while delivering solutions that make a difference locally., • Career Growth – Expand your skills through mentorship, professional development, technical training, and leadership opportunities., • Culture of Collaboration – Thrive in an inclusive environment where diverse perspectives are valued, innovation is encouraged, and teamwork drives success., • Opportunity to Grow with Us – Join a rapidly expanding organization where your ideas, contributions, and career can grow alongside the business. Total Rewards That Support You We believe great work starts with supporting our people. That's why Egis offers a comprehensive Total Rewards program designed to promote your health, well-being, financial security, and professional growth, including: • Competitive medical, dental, and vision coverage, • 401(k) retirement plan with company match, • Paid time off and flexible holiday program, • Flexible work arrangements, including hybrid and remote opportunities where business needs allow, • Life insurance and disability coverage, including maternity leave, • Health Savings Account (HSA) with employer contributions, • Flexible Spending Accounts (FSA) for healthcare and dependent care expenses, • Paid family leave, • Wellness programs supporting physical and mental well-being, • Education assistance, professional development, and continuing learning opportunities, • Employee Assistance Program (EAP), • Employee discount programs At Egis, we're committed to creating an environment where talented people can do their best work, continue to grow professionally, and build rewarding, long-term careers. Compensation & Pay Transparency At Egis, we believe transparency helps candidates make informed career decisions. As part of our commitment to an open and equitable hiring process, we've included the anticipated base salary range for this position below. Equal Employer Egis is proudly committed to recruiting and retaining a diverse and inclusive workforce. Egis provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. All positions at Egis require an applicant who has accepted an employment offer to undergo pre-employment screening. Background checks include SSN/SIN validation, motor vehicle verification, education verification, employment verification, a criminal check, search against global sanctions and government watch lists, and drug tests. All employment offers are contingent upon successful results of the pre-employment screening. Privacy Policies

Job Description HCR0003329 Title: Lab Technician Pay : 23-24/HR on W2 3-5 days in office, averaging 30 hrs/week Job Summary: We are seeking a detail-oriented Lab Technician to support preclinical and benchtop testing for a medical device. The ideal candidate will have hands-on laboratory experience with tissue preparation and sectioning, and an interest in or exposure to engineering laboratory instrumentation and test equipment. This role involves executing test protocols, operating laboratory and acoustic test equipment, and recording data to Good Documentation Practices (GDP). Experience in a regulated medical device environment is highly desirable. This position is open to candidates with a minimum of 2 years of laboratory experience. Key Responsibilities: • Prepare, condition and process ex vivo tissue samples according to work instructions., • Perform treatments on tissue samples and routine histology procedures., • Section tissue using a cryostat and acquire images using microscopy or slide scanning systems., • Set up and perform routine acoustic characterization and measurements on ultrasound transducers using hydrophone-based test systems., • Manage, organize, and maintain raw data collected from acoustic measurement systems., • Execute test protocols and record data accurately and in real time following GDP., • Document deviations and escalate issues promptly., • Perform routine checks of equipment calibration and maintenance status before use., • Maintain lab supplies, sample inventory and a clean, organized work environment., • Collaborate with engineers to support testing and improve lab processes. Qualifications: • Bachelor's degree in biology, biomedical engineering, physics or a related field, or equivalent laboratory experience., • Minimum of 2 years of laboratory experience., • Experience with tissue preparation, cryosectioning or histology techniques., • Familiarity with general test equipment and instrumentation, including oscilloscopes, pulsers/receivers, and data acquisition hardware/software., • Experience with hydrophone-based ultrasound measurements is a plus., • Experience with GDP, and with GLP or a regulated medical device environment (ISO 13485) is a plus., • Comfortable working with ex vivo animal tissue., • Strong attention to detail and excellent organizational skills., • Ability to follow detailed procedures, and to work independently and as part of a team., • Good communication skills. Work Schedule: Flexible part-time hours, on site, with the possibility of additional hours based on business needs. Kindly share resume with answers: Q1: Tell me about your laboratory experience. How many years have you worked in a lab, and what testing or sample preparation have you personally performed? Q2: What experience do you have preparing tissue samples, performing histology, or using a cryostat?

Job DescriptionAt Whitman, Requardt & Associates, LLP, we are "People Focused and Project Driven". We have been in business for more than 110 years and we are known for our quality work and developing quality employee careers. We are seeking the very best and most talented to join our team - help us take on today’s infrastructure challenges, develop advanced vision and innovative ideas, and design solutions for resilient, sustainable, efficient and effective multi-modal infrastructure improving and connecting our Communities, States, Countries, and World. We are currently seeking a Project Environmental Scientist/Planner in our Raleigh, NC office who is looking for growth opportunities and enjoys working on a wide variety of projects. Responsibilities: The candidate for this position will lead natural system surveys, field investigations, and delineations including wetland delineations, conducting threatened and endangered species habitat evaluations and surveys, assist, support and prepare National Environmental Policy Act (NEPA) and State Environmental Policy Act (SEPA) documentation, planning and feasibility studies, and public outreach. The candidate will also lead Section 404/401 permitting, coordinate with regulatory agencies and clients, conduct permit compliance monitoring, conduct bat bridge inspections, conduct surveys for invasive species, prepare invasive species management plans, assist with stream stabilization/restoration projects, mentor and train junior staff, and any other services as required by specific projects. The candidate must have knowledge of and experience with the development of NEPA/ SEPA documents for State DOTs, FHWA, or FTA. The candidate would work collaboratively with teams on complex environmental documents, would manage projects and tasks commensurate to experience, and would be responsible for preparing environmental documents and supporting technical analyses. The individual will assist with work planning and scheduling, managing project budgets and scopes, with Business Development, including proposal preparation. The candidate will participate in the planning of transportation related projects. They must be innovative and adaptive at identifying problems and finding solutions. Responsibilities will also include assuring highest quality and deliverable expectations are always maintained. Periodic travel (including overnight) will be required to conduct field work and/or attend project meetings, as needed. Requirements: • Bachelor's degree in Environmental Planning, Biology, Geology, Environmental Engineering, Environmental Science, Natural Resources Management, or related field. Master's degree preferred., • 11 - 15 years of experience desired in the environmental compliance discipline but will consider less years’ experience for significant relevant experience in environmental documentation (all levels), ecological studies, wetland, and stream delineations, threatened and endangered species studies, environmental permitting, or related environmental compliance., • Thorough knowledge of NEPA/environmental planning practices and procedures as well as experience in preparing NEPA documents in accordance with the US DOT guidelines and specific State DOTs’ requirements., • Broad knowledge of environmental laws and regulations, which include but are not limited to NEPA and the Clean Water Act (CWA)., • Experience in performing ecological studies, wetland, and stream delineations, threatened and endangered species surveys and studies, and knowledge of CWA permitting processes., • Experience with NCDOT Natural Resource Technical Reports, Guidance, and Procedures., • Experience obtaining Section 404/401 permits., • Experience coordinating with federal and state resource agencies., • Ability to handle multiple projects and deadlines., • Experience authoring and reviewing environmental documentation., • Excellent technical writing and oral communication skills., • Positive attitude and ability to interact and communicate/work with multidisciplinary team members., • Ability to work independently and as part of a team in coordination with multiple offices., • Experience with Microsoft Office (Word, Excel, Outlook), TEAMS and GIS analysis tools is required., • Strong plant identification skills., • Willingness to continue to learn and grow technically and professionally within the company., • Willingness to mentor and train junior staff., • Ability to interpret and stay abreast of environmental regulations. Desired Requirements: • Certification or professional registration is a plus., • Recent, relevant experience working with federal, and regional states regulatory agencies a plus., • Experience managing projects, scopes, budgets, and staff with limited oversight/supervision is a plus., • Experience in any of the following states, VA, MD, WV, SC, GA, FL, DE and PA is a plus. Benefits: WRA recognizes that employees play an important role in its success. Our commitment to full-time employees is reflected in the comprehensive benefits package we offer: • Flexible work schedule options, • Competitive salary, • Leave accrual and paid holidays, • Healthcare benefits, • Group Life Insurance, as well as additional optional life Insurance, short and long term disability insurance, • Flexible spending accounts for medical and dependent care reimbursement, • 401(k) Retirement Plan, • Tuition Reimbursement, • Employee Assistance Program, • Parental and maternity leave benefits WRA is an equal opportunity/affirmative action employer and complies with all applicable anti-discrimination laws. Applicants must be currently authorized to work in the United States on a full-time basis without the need for employment-based visa sponsorship now or in the future. WRA will not sponsor applicants for U.S. work visa status for this opportunity. (no sponsorship is available for H-1B, L-1, TN, O-1, E-3, H-1B1, F-1, J-1, OPT, CPT or any other employment-based visa) * Not accepting resumes from 3rd party recruiters for this position * Position # 3232 #LI - Mid-Level #Onsite

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 Carbon Cycle North Carolina, LLC (C2NC) Location: Plant-based position located at the Carbon Cycle North Carolina facility in Warsaw, North Carolina Job: Laboratory Technician Hiring Manager: Lab Manager Carbon Cycle North Carolina LLC is seeking a skilled Laboratory Technician to support the safe, reliable, and efficient operation of its anaerobic digestion and renewable natural gas facility in Warsaw, North Carolina. This hands-on role supports the operation of the biogas facility by conducting routine laboratory analysis of digestate, filtrate, wastewater, and separated solids. The role focuses on monitoring key parameters to help ensure stable plant performance and regulatory compliance. Facility Overview As global industries face increasing pressure to decarbonize, renewable natural gas (RNG) is emerging as a practical and scalable solution. C2NC is building the infrastructure to support that transition - turning overlooked resources into clean energy while prioritizing transparency, environmental integrity, and operational precision. Here's how we're moving forward. C2NC develops and operates industrial-scale anaerobic digestion facilities that transform organic byproducts into pipeline-grade renewable natural gas. These facilities not only reduce methane emissions but also offer a sustainable, circular alternative to traditional energy sourcing. Our flagship site in Warsaw, NC is one of the largest of its kind in the Southeast - and it's just the beginning. The Warsaw facility receives agricultural and organic feedstocks, produces pipeline-quality renewable natural gas, manages digestate, and treats process wastewater through an on-site membrane bioreactor system. Position Summary The Laboratory Technician supports the operation of the biogas facility by conducting routine laboratory analysis of digestate, filtrate, wastewater, and separated solids. The role focuses on monitoring key parameters to help ensure stable plant performance and regulatory compliance. Key Responsibilities • Collect and prepare samples from plant process streams, • Perform routine analyses including but not limited to: pH, Chemical Oxygen Demand (COD), Dissolved Oxygen, Ammonia-Nitrogen, Volatile Fatty Acids, Alkalinity, solids analyses, • Record, verify, and report laboratory data to laboratory management, • Maintain laboratory instruments, perform calibrations, and troubleshoot as necessary, • Maintain basic laboratory cleanliness and adhere to safety regulations Qualifications • Associate’s or Bachelor’s degree in Chemistry, Environmental Science, Biology, or any related field, • 1-3 years of laboratory experience, • Strong attention to detail and basic data analysis skills, • Ability to follow SOP’s and maintain accurate records, • Ability to work independently Required Skills and Competencies • Lab equipment operation and calibration., • Sample preparation and aseptic technique., • Quality control, interpreting charts, and spot out-of-range anomalies., • Laboratory software and data entry., • Safety and sterilization. Preferred Experience • Background in a manufacturing, renewable natural gas, anaerobic digestion, wastewater, or similar industrial-process environment., • Familiarity with lab equipment used to analyze and document test results., • Practical knowledge of experimental techniques used in scientific work. Work Environment and Schedule Combination of laboratory and industrial plant environment with regular exposure to outdoor conditions and biological materials. Compensation and Benefits Compensation is $28 to $38 per hour. Benefits may include medical, dental, vision, life insurance, paid time off, and retirement benefits, subject to applicable plan terms and eligibility requirements. C2NC is an equal opportunity employer and considers qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, or any other status protected by applicable law. \nCompany Description Carbon Cycle Biogas (C2 Biogas) develops utility-scale solutions that turn organic waste into clean-burning renewable natural gas. C2 Biogas’s plant is one of the largest biogas facilities in North America: an in-house designed, 100-foot high industrial complex producing pipeline-quality RNG, which can reliably power the equivalent of tens of thousands of homes. C2 Biogas turns environmental regulatory requirements into economic opportunity—providing a path to compliance that generates revenue instead of costs by transforming waste into RNG. Carbon Cycle Biogas (C2 Biogas) develops utility-scale solutions that turn organic waste into clean-burning renewable natural gas. C2 Biogas’s plant is one of the largest biogas facilities in North America: an in-house designed, 100-foot high industrial complex producing pipeline-quality RNG, which can reliably power the equivalent of tens of thousands of homes. C2 Biogas turns environmental regulatory requirements into economic opportunity—providing a path to compliance that generates revenue instead of costs by transforming waste into RNG.

Job Description Andrology Laboratory Technologist Atlantic Fertility | Full-Time About the Position Atlantic Fertility is seeking a motivated, detail-oriented Andrology Laboratory Technologist to join our team. This entry- to mid-level position is ideal for someone with experience in an IVF laboratory who is looking to build on their technical skills and contribute to high-quality, patient-centered fertility care. The ideal candidate is dependable, organized, and comfortable working independently while collaborating with a multidisciplinary clinical team. We value attention to detail, strong communication skills, and a commitment to maintaining the highest standards of laboratory quality and patient safety. Key Responsibilities • Independently perform semen analyses, including preparing specimen collection kits and providing patient instructions as needed., • Process specimens for intrauterine insemination (IUI), therapeutic donor insemination (TDI), IVF, and cryopreservation., • Respond to patient inquiries through the electronic medical record (EMR) patient portal and obtain informed consent for procedures as needed., • Perform delegated daily, weekly, monthly, and annual quality control (QC), equipment maintenance, and laboratory maintenance tasks., • Maintain laboratory inventory of reagents and consumables, including gases, liquid nitrogen, culture media, and other essential supplies., • Maintain accurate laboratory documentation and follow established protocols for specimen identification, handling, and processing., • Adhere to laboratory safety procedures, quality assurance standards, and applicable regulatory and accreditation requirements., • Collaborate with embryology, nursing, and clinical staff to support efficient daily laboratory operations. Qualifications • Bachelor's degree in biology, or chemistry, or clinical laboratory science.., • Experience in an IVF or andrology laboratory preferred., • Foundational knowledge of semen analysis and sperm processing techniques., • Strong attention to detail, organizational skills, and commitment to accuracy., • Excellent written and verbal communication skills, including the ability to interact professionally with patients., • Ability to work independently, follow established protocols, and prioritize tasks in a fast-paced clinical environment., • Participation in weekend and holiday rotation is required. What We Offer • Comprehensive employee benefits package including medical, dental, vision insurance., • 401(k) retirement plan with employer matching., • A collaborative and supportive team environment., • Opportunities to expand technical knowledge and develop professionally in reproductive laboratory science. Join Our Team At Atlantic Fertility, our laboratory team plays an essential role in helping patients build their families. If you have a foundation in IVF laboratory work, take pride in the quality of your work, and are eager to grow your skills in andrology, we invite you to apply.

Job Description 3-5 days in office, averaging 30 hrs/week Job Summary: We are seeking a detail-oriented Lab Technician to support preclinical and benchtop testing for a medical device. The ideal candidate will have hands-on laboratory experience with tissue preparation and sectioning, and an interest in or exposure to engineering laboratory instrumentation and test equipment. This role involves executing test protocols, operating laboratory and acoustic test equipment, and recording data to Good Documentation Practices (GDP). Experience in a regulated medical device environment is highly desirable. This position is open to candidates with a minimum of 2 years of laboratory experience. Key Responsibilities: • Prepare, condition and process ex vivo tissue samples according to work instructions., • Perform treatments on tissue samples and routine histology procedures., • Section tissue using a cryostat and acquire images using microscopy or slide scanning systems., • Set up and perform routine acoustic characterization and measurements on ultrasound transducers using hydrophone-based test systems., • Manage, organize, and maintain raw data collected from acoustic measurement systems., • Execute test protocols and record data accurately and in real time following GDP., • Document deviations and escalate issues promptly., • Perform routine checks of equipment calibration and maintenance status before use., • Maintain lab supplies, sample inventory and a clean, organized work environment., • Collaborate with engineers to support testing and improve lab processes. Qualifications: • Bachelor's degree in biology, biomedical engineering, physics or a related field, or equivalent laboratory experience., • Minimum of 2 years of laboratory experience., • Experience with tissue preparation, cryosectioning or histology techniques., • Familiarity with general test equipment and instrumentation, including oscilloscopes, pulsers/receivers, and data acquisition hardware/software., • Experience with hydrophone-based ultrasound measurements is a plus., • Experience with GDP, and with GLP or a regulated medical device environment (ISO 13485) is a plus., • Comfortable working with ex vivo animal tissue., • Strong attention to detail and excellent organizational skills., • Ability to follow detailed procedures, and to work independently and as part of a team., • Good communication skills. Work Schedule: Flexible part-time hours, on site, with the possibility of additional hours based on business needs. \nCompany Description At AA2IT, we deliver solutions that align with your business goals, built on innovation, backed by a team of experts, and guided by measurable outcomes. At AA2IT, we deliver solutions that align with your business goals, built on innovation, backed by a team of experts, and guided by measurable outcomes.

Job Description Title: Lab Technician 3-5 days in office, averaging 30 hrs/week Job Summary: We are seeking a detail-oriented Lab Technician to support preclinical and benchtop testing for a medical device. The ideal candidate will have hands-on laboratory experience with tissue preparation and sectioning, and an interest in or exposure to engineering laboratory instrumentation and test equipment. This role involves executing test protocols, operating laboratory and acoustic test equipment, and recording data to Good Documentation Practices (GDP). Experience in a regulated medical device environment is highly desirable. This position is open to candidates with a minimum of 2 years of laboratory experience. Key Responsibilities: • Prepare, condition and process ex vivo tissue samples according to work instructions., • Perform treatments on tissue samples and routine histology procedures., • Section tissue using a cryostat and acquire images using microscopy or slide scanning systems., • Set up and perform routine acoustic characterization and measurements on ultrasound transducers using hydrophone-based test systems., • Manage, organize, and maintain raw data collected from acoustic measurement systems., • Execute test protocols and record data accurately and in real time following GDP., • Document deviations and escalate issues promptly., • Perform routine checks of equipment calibration and maintenance status before use., • Maintain lab supplies, sample inventory and a clean, organized work environment., • Collaborate with engineers to support testing and improve lab processes. Qualifications: • Bachelor's degree in biology, biomedical engineering, physics or a related field, or equivalent laboratory experience., • Minimum of 2 years of laboratory experience., • Experience with tissue preparation, cryosectioning or histology techniques., • Familiarity with general test equipment and instrumentation, including oscilloscopes, pulsers/receivers, and data acquisition hardware/software., • Experience with hydrophone-based ultrasound measurements is a plus., • Experience with GDP, and with GLP or a regulated medical device environment (ISO 13485) is a plus., • Comfortable working with ex vivo animal tissue., • Strong attention to detail and excellent organizational skills., • Ability to follow detailed procedures, and to work independently and as part of a team., • Good communication skills. Work Schedule: Flexible part-time hours, on site, with the possibility of additional hours based on business needs. \nCompany Description At AA2IT, we deliver solutions that align with your business goals, built on innovation, backed by a team of experts, and guided by measurable outcomes. At AA2IT, we deliver solutions that align with your business goals, built on innovation, backed by a team of experts, and guided by measurable outcomes.

Job Description Carbon Cycle North Carolina, LLC (C2NC) Location: Plant-based position located at the Carbon Cycle North Carolina facility in Warsaw, North Carolina Job: Laboratory Technician Hiring Manager: Lab Manager Carbon Cycle North Carolina LLC is seeking a skilled Laboratory Technician to support the safe, reliable, and efficient operation of its anaerobic digestion and renewable natural gas facility in Warsaw, North Carolina. This hands-on role supports the operation of the biogas facility by conducting routine laboratory analysis of digestate, filtrate, wastewater, and separated solids. The role focuses on monitoring key parameters to help ensure stable plant performance and regulatory compliance. Facility Overview As global industries face increasing pressure to decarbonize, renewable natural gas (RNG) is emerging as a practical and scalable solution. C2NC is building the infrastructure to support that transition - turning overlooked resources into clean energy while prioritizing transparency, environmental integrity, and operational precision. Here's how we're moving forward. C2NC develops and operates industrial-scale anaerobic digestion facilities that transform organic byproducts into pipeline-grade renewable natural gas. These facilities not only reduce methane emissions but also offer a sustainable, circular alternative to traditional energy sourcing. Our flagship site in Warsaw, NC is one of the largest of its kind in the Southeast - and it's just the beginning. The Warsaw facility receives agricultural and organic feedstocks, produces pipeline-quality renewable natural gas, manages digestate, and treats process wastewater through an on-site membrane bioreactor system. Position Summary The Laboratory Technician supports the operation of the biogas facility by conducting routine laboratory analysis of digestate, filtrate, wastewater, and separated solids. The role focuses on monitoring key parameters to help ensure stable plant performance and regulatory compliance. Key Responsibilities • Collect and prepare samples from plant process streams, • Perform routine analyses including but not limited to: pH, Chemical Oxygen Demand (COD), Dissolved Oxygen, Ammonia-Nitrogen, Volatile Fatty Acids, Alkalinity, solids analyses, • Record, verify, and report laboratory data to laboratory management, • Maintain laboratory instruments, perform calibrations, and troubleshoot as necessary, • Maintain basic laboratory cleanliness and adhere to safety regulations Qualifications • Associate’s or Bachelor’s degree in Chemistry, Environmental Science, Biology, or any related field, • 1-3 years of laboratory experience, • Strong attention to detail and basic data analysis skills, • Ability to follow SOP’s and maintain accurate records, • Ability to work independently Required Skills and Competencies • Lab equipment operation and calibration., • Sample preparation and aseptic technique., • Quality control, interpreting charts, and spot out-of-range anomalies., • Laboratory software and data entry., • Safety and sterilization. Preferred Experience • Background in a manufacturing, renewable natural gas, anaerobic digestion, wastewater, or similar industrial-process environment., • Familiarity with lab equipment used to analyze and document test results., • Practical knowledge of experimental techniques used in scientific work. Work Environment and Schedule Combination of laboratory and industrial plant environment with regular exposure to outdoor conditions and biological materials. Compensation and Benefits Compensation is $28 to $38 per hour. Benefits may include medical, dental, vision, life insurance, paid time off, and retirement benefits, subject to applicable plan terms and eligibility requirements. C2NC is an equal opportunity employer and considers qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, or any other status protected by applicable law. \nCompany Description Carbon Cycle Biogas (C2 Biogas) develops utility-scale solutions that turn organic waste into clean-burning renewable natural gas. C2 Biogas’s plant is one of the largest biogas facilities in North America: an in-house designed, 100-foot high industrial complex producing pipeline-quality RNG, which can reliably power the equivalent of tens of thousands of homes. C2 Biogas turns environmental regulatory requirements into economic opportunity—providing a path to compliance that generates revenue instead of costs by transforming waste into RNG. Carbon Cycle Biogas (C2 Biogas) develops utility-scale solutions that turn organic waste into clean-burning renewable natural gas. C2 Biogas’s plant is one of the largest biogas facilities in North America: an in-house designed, 100-foot high industrial complex producing pipeline-quality RNG, which can reliably power the equivalent of tens of thousands of homes. C2 Biogas turns environmental regulatory requirements into economic opportunity—providing a path to compliance that generates revenue instead of costs by transforming waste into RNG.

Job Description ERG is a research and consulting firm that provides a wide range of support to federal, state, and commercial clients. ERG offers multidisciplinary teams with nationally recognized skills in engineering, science, economics, public health, informational technology, and communications. We hire people with the best minds and then provide them with a vibrant and flexible environment in which to develop their careers. The qualified individual must be highly motivated with the skills to prioritize, perform, and communicate effectively in a fast-paced environment. ERG is hiring enthusiastic and highly motivated Junior Engineers, Scientists, and Technicians to provide technical support in the development, design, and execution of research projects for the U.S. Environmental Protection Agency’s (EPA) Office of Research and Development. Research activities may include decontamination and consequence management studies; development and validation of measurement methods, source emission characterization, and data collection; research in atmospheric sciences, physical, chemical, biological, toxicological, and human and ecological exposure; development, evaluation, and application of air quality simulation modeling in the Fluid Modeling Facility/Meteorological Wind Tunnel; and other related research initiatives. Work will take place in specialized laboratories and machine shops, including fabrication machine shops, metrology laboratories, and other analytical and microbiological labs. As a junior professional, you will play a key role in designing, developing, and optimizing solutions while executing technical projects. This is an excellent opportunity for recent graduates or early-career professionals to gain hands-on experience while collaborating with seasoned experts. The ideal candidate will have a strong technical foundation, excellent problem-solving abilities, and the ability to work effectively across teams to drive innovation. You will work closely with senior staff to contribute to work plans, quality assurance project plans (QAPPs), health and safety plans, and reports for projects conducted by ERG. Job Description: • Assist in the design, development, and testing of new processes or experiments under the guidance of senior engineers, scientists, or technicians, • Support the preparation of technical reports, data analysis, and project documentation, • Troubleshoot, maintain, calibrate, and repair laboratory and field equipment and instruments, • Execute technical projects under the direction of senior staff, • Collaborate with cross-functional teams to develop and implement innovative engineering or scientific solutions, • Follow all safety guidelines and requirements in the lab or field, ensuring compliance with company policies, • Contribute to ongoing projects by collecting data, performing tests, and compiling results, • Assist in preparing project plans, schedules, and materials necessary for project execution, • Evaluate emerging technologies, tools, and processes for potential integration into current and future projects, • Apply best practices, methodologies, and cutting-edge techniques to support project objectives, • Conduct advanced research, analysis, design, and testing to support project development and optimization, • Present technical findings, project progress, and results under the guidance of senior staff to leadership, clients, or at conferences as appropriate, • Work closely with senior staff to gain hands-on exposure to project management, design processes, and technical problem-solvingQualifications and Skills:, • B.S. degree in Environmental, Mechanical, or Chemical Engineering, Chemistry, Physics, Biology, Environmental Science, or a related field, • Relevant experience in lieu of a degree will be considered, • Strong analytical, mechanical, and problem-solving skills, with demonstrated aptitude and interest in science, technical work, mechanical equipment, and air quality, • 3+ years of experience providing on-site research support for the EPA’s Office of Research and Development, • Experience authoring scientific, technical, quality assurance, and health & safety documentation, • Hands-on experience in a laboratory, technical setting, or engineering project (academic or professional), • Experience in mechanical work, laboratory research, or field science preferred, • Knowledge of EPA source test methods/procedures, air quality monitoring, and emissions measurement equipment preferred, • Ability and willingness to travel as needed for field projects across the country, • Ability to pass background checks and both initial and random drug screenings ERG offers competitive salaries and excellent benefits, including health and dental insurance, life insurance, long-term disability, educational benefits, FSAs, a generous 401k plan, profit sharing, an EAP, 11-20 paid vacation days per year, 10 paid holidays per year, 56 hours or more of sick leave (based on the state you work in) per year (pro-rated for part-time) and more. The salary range for all positions depends on the years and type of experience. ERG is an equal opportunity employer and complies with all applicable EEOC regulations. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual preference, national origin, disability, or status as a protected veteran. Please be aware, the only authentic corporate domain for ERG is https://www.erg.com. ERG may, on occasion, screen applicants via telephone or video interviews via Skype, Teams, GoToMeeting, or another type of video platform. However, any candidate extended a job offer might be asked to meet in person with an ERG employee before providing confidential personal information associated with new employment. If you’re a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access ERG’s online application process as a result of your disability. To request accommodation, please contact Human Resources via email at Resumes-Lex@erg.com or call (781) 674-7293. ERG fosters a friendly, flexible work environment. ERGers are dedicated to serving clients who are committed to making the world a better place. We promote and recognize principles of fairness and respect in the work we do, the partnerships we foster, and the culture we value both within and outside of our organization.

Job Description ERG is a research and consulting firm that provides a wide range of support to federal, state, and commercial clients. ERG offers multidisciplinary teams with nationally recognized skills in engineering, science, economics, public health, informational technology, and communications. We hire people with the best minds and then provide them with a vibrant and flexible environment in which to develop their careers. The qualified individual must be highly motivated with the skills to prioritize, perform, and communicate effectively in a fast-paced environment. ERG is hiring enthusiastic and highly motivated entry-level engineers, scientists, chemists, and technicians to provide technical support in the development, design, and execution of research projects for the U.S. EPA’s Office of Research and Development. Research activities may include decontamination and consequence management research; development and validation of measurement methods; source emission characterization and data collection; studies in atmospheric sciences, physical, chemical, biological, toxicological, and human and ecological exposure; development, evaluation, and application of air quality simulation modeling in the Fluid Modeling Facility/Meteorological Wind Tunnel; and other related research initiatives. Work will involve specialized laboratories and machine shops, including fabrication machine shops, metrology laboratories, and other analytical and microbiological laboratories. As an entry-level professional, you will play an integral role in designing, developing, and optimizing solutions while executing technical projects. This is an excellent opportunity for recent graduates or early-career professionals to gain hands-on experience while collaborating with seasoned experts. The ideal candidate will have a strong technical foundation, excellent problem-solving abilities, and the capability to work effectively across teams to drive innovation. You will also provide input to senior staff in preparing work plans, quality assurance project plans (QAPPs), health and safety plans, and reports for projects performed by ERG. Job Description: • Assist in designing, developing, and testing new processes or experiments under the guidance of senior engineers, scientists, or technicians, • Support the preparation of technical reports, data analysis, and project documentation, • Troubleshoot, maintain, calibrate, and repair laboratory and field equipment, • Execute technical projects under the direction of senior staff, • Collaborate with cross-functional teams to develop and implement innovative engineering or scientific solutions, • Follow all safety protocols and requirements in laboratory and field settings, ensuring compliance with company policies, • Contribute to ongoing projects by collecting data, performing tests, and compiling results, • Assist in preparing project plans, schedules, and materials needed for project execution, • Present technical findings, project progress, and results under the guidance of senior staff to leadership, clients, or at conferences as appropriate, • Work closely with senior staff to gain hands-on exposure to project management, design processes, and technical problem-solvingQualifications and Skills:, • B.S. degree in Environmental, Mechanical, or Chemical Engineering, Chemistry, Physics, Biology, Environmental Science, or a related field, • Relevant experience in lieu of a degree will be considered, • Strong analytical, mechanical, and problem-solving skills, • Demonstrated aptitude and interest in science, technical work, mechanical equipment, chemistry, and air quality, • Hands-on experience in a laboratory, technical setting, or engineering project (academic or professional), • Experience in mechanical work, laboratory research, or field science preferred, • Knowledge of EPA source test methods/procedures, air quality or emissions monitoring equipment, and related techniques preferred, • Ability to travel as needed for field projects across the country, • Ability to pass background checks and initial and random drug screenings, • Commercial Driver’s License (CDL) preferred, or equivalent experience hauling trailers over long distances ERG offers competitive salaries and excellent benefits, including health and dental insurance, life insurance, long-term disability, educational benefits, FSAs, a generous 401k plan, profit sharing, an EAP, 11-20 paid vacation days per year, 10 paid holidays per year, 56 hours or more of sick leave (based on the state you work in) per year (pro-rated for part-time) and more. The salary range for all positions depends on the years and type of experience. ERG is an equal opportunity employer and complies with all applicable EEOC regulations. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual preference, national origin, disability, or status as a protected veteran. Please be aware, the only authentic corporate domain for ERG is https://www.erg.com. ERG may, on occasion, screen applicants via telephone or video interviews via Skype, Teams, GoToMeeting, or another type of video platform. However, any candidate extended a job offer might be asked to meet in person with an ERG employee before providing confidential personal information associated with new employment. If you’re a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access ERG’s online application process as a result of your disability. To request accommodation, please contact Human Resources via email at Resumes-Lex@erg.com or call (781) 674-7293. ERG fosters a friendly, flexible work environment. ERGers are dedicated to serving clients who are committed to making the world a better place. We promote and recognize principles of fairness and respect in the work we do, the partnerships we foster, and the culture we value both within and outside of our organization.

Job Description Part-Time Math & Science Teacher Flexible Schedule | No Lesson Planning or Outside Work | One-to-One Instruction $22-23/hour What if teaching meant focusing on just one student at a time? At Brightmont Academy, that’s exactly what we do. Since 1999, we’ve helped students in grades 1–12 achieve their full potential through personalized one-to-one instruction. With 28 campuses across 11 states, we create a nurturing, student-centered environment where meaningful learning happens every day. Why You’ll Love Our 1:1 Teaching Model: • Be the Star of the Show! Teach students one-on-one, tailoring lessons to their unique needs and learning styles., • Empower Young Minds: Guide students to mastery with a gradual release approach that builds confidence and academic success., • No Stress, No Extra Work: Forget about lesson planning, parent conferences, or endless grading. We want you to focus on inspiring your students!, • Grow With Us: Enjoy professional development opportunities that elevate your teaching career. Requirements • A Bachelor’s Degree in your subject area (Math, Chemistry, Physics, Engineering, Biology—anything that fuels your passion!)., • Patience & Empathy: You understand that every student learns differently, and you’re committed to supporting them every step of the way., • A Heart for Teaching: A genuine passion to share your subject with the next generation., • Proficiency using G-Suite and Learning Management Software (LMS)., • Ability to provide fingerprints (AZ, WA, only) and pass a federal background check. Bonus Qualifications: • A teaching certification - nice to have, but not required!, • Advanced degree in a specific subject area of expertise., • Previous one-to-one teaching experience. Brightmont Academy is an equal opportunity employer. Our intent is to recruit, hire, and train all persons in all job groups in accordance with the law, without regard to race, color, religion, sex, age, marital status, disability, national origin, sexual preference, or any other protected status. Keywords: Math / Algebra / Calculus / Geometry / Trigonometry / Chemistry / Biology / Physics / Zoology / Astronomy / Teacher / Tutor / Professor / Instructor / Adjunct Powered by JazzHR y6GiEP7Ufq

Job DescriptionFine Gardening Crew Leader $65,000-$80,000 salary + bonus Lead detailed garden care for premium landscapes where plant knowledge and an exceptional eye for detail matter. Currin Outdoor Living is seeking a Fine Gardening Crew Leader to oversee high-end garden care and routine landscape maintenance, with special emphasis on ornamental plants, flowers, shrubs, seasonal displays, and meticulous property presentation. At Currin Outdoor Living, our mission is simple: To honor God by creating spaces that help foster and build better relationships. We're guided by integrity, excellence, accountability, and teamwork - and we welcome employees of all beliefs who share those values.Compensation & Benefits • $65,000-$80,000 salary + bonus, • Health Insurance, • Retirement Plan, • Paid Time Off and Holiday Pay, • Professional Development Opportunities, • Company Cell PhoneWhat You'll Do, • Perform and oversee detailed hand pruning, deadheading, weeding, plant-health checks, and perennial/annual flower care., • Delegate and supervise lawn mowing, string trimming, edging, and general grounds maintenance., • Safely drive a truck and trailer to jobsites., • Maintain equipment used by the crew., • Ensure work is completed safely, efficiently, and to a high aesthetic standard., • Communicate with clients about daily work, future needs, out-of-scope opportunities, and property expectations.What We're Looking For, • 2 years of experience in fine gardening, horticulture, or detailed landscape maintenance., • 2 years of crew-lead experience in landscape maintenance or fine gardening., • Valid driver's license with a clean driving record., • Strong knowledge of ornamental plants, shrubs, flowers, pruning techniques, and equipment operation., • Strong attention to detail.What Will Help You Stand Out, • Degree or certification in horticulture, plant biology, landscape maintenance, or a related field is a plus., • Strong communication skills., • Exceptional eye for floral care, plant health, bed styling, and ornamental garden presentation., • Computer skills and experience with LMN Time or similar landscape software are a plus.Physical & Work EnvironmentThis is an active outdoor leadership position. Candidates must be able to frequently lift up to 50 pounds and occasionally lift up to 80 pounds and work in changing weather, noise, dust, pollen, wet conditions, and around landscape equipment. Travel to jobsites throughout the Triangle area is required using a company vehicle. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Why Currin Outdoor Living?We're not your average landscape company. We create and care for premium outdoor environments with creativity, precision, and pride. You'll be part of a growing team that values quality work, accountability, teamwork, and professional development. Ready to take the next step? Apply today. We'd love to hear from you.Equal Opportunity EmployerCurrin Outdoor Living is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to legally protected characteristics in accordance with applicable federal, state, and local laws. Military-experienced candidates are encouraged to apply. Powered by JazzHR C7hyDqWMR3

MMRF OVERVIEW: The Multiple Myeloma Research Foundation (MMRF) is the largest nonprofit in the world solely focused on accelerating a cure for each and every multiple myeloma patient. We drive the development and delivery of next-generation therapies, leverage data to identify optimal and more personalized treatment approaches, and empower myeloma patients and the broader community with information and resources to extend their lives. Central to our mission is our commitment to advancing health equity so that all myeloma patients can benefit from the scientific and clinical advances we pursue. Since our inception, the MMRF has committed over $600 million for research, opened nearly 100 clinical trials, and helped bring 15+ FDA-approved therapies to market, which have tripled the life expectancy of myeloma patients. To learn more, visit www.themmrf.org. MMRF Core Values: At the MMRF our core values define both who we are and how we work together as an organization. We believe in investing in our team and building a culture that will help us pursue our highest level mission to accelerate a cure for each and every multiple myeloma patient. Our five core values are expressed below: • Prioritize Patients - Patients are at the center of everything we do. Every decision we make is grounded in the needs and best interests of the patients we serve., • Drive Innovation - We are committed to pursuing big, bold ideas. Taking risks, trying new approaches, and challenging the status quo are necessary to speed new discoveries., • Deliver Solutions - Taking on complicated challenges is what sets us apart. To deliver results, we must be decisive, take action, and act with urgency on behalf of the myeloma community., • Do It Together - We know that together, we are stronger. We work cross-functionally with the entire community to achieve our mission and are invested in the success of others., • Build Trust - We build trust-based relationships. We advocate for each and every myeloma patient by committing to diversity, equity, and inclusion and treating others with respect. Position Overview: The MMRF is seeking an experienced computational biologist to serve as Scientist / Lead, Translational Data Platforms for the MMRF Virtual Lab, our cloud-native translational research platform accelerating discoveries for the global multiple myeloma research community. This is a unique opportunity for a computational scientist who is passionate about translating complex biological questions into scalable technology solutions that empower researchers around the world. The successful candidate will combine expertise in computational biology, cancer genomics, and scientific analysis with product leadership, stakeholder engagement, and program management to drive the continued evolution of one of the world's leading myeloma-focused multi-omic research platforms. Working closely with the Director of Translational Research, you will assume day-to-day ownership of the Virtual Lab product roadmap, helping define the future direction of a next-generation computational research platform at the intersection of translational science, cloud technologies, artificial intelligence, and product innovation. You will work collaboratively with computational biologists, software engineers, clinicians, cloud architects, academic collaborators, technology partners, and scientific leadership to translate research priorities into innovative platform capabilities that accelerate biomedical discovery. This role is specifically designed for a computational scientist who wishes to remain actively engaged in scientific research while leading the development and evolution of research software products. You will continue contributing to computational analyses, development of bioinformatics workflows, translational research, scientific publications, and conference presentations, ensuring that scientific discovery remains central to your role while serving as the scientific owner of the platform. As Scientist / Lead, Translational Data Platforms, you will play a pivotal role in shaping how researchers interact with complex clinical and multi-omic datasets, influencing platform strategy, developing innovative analytical capabilities, and helping build technologies that enable the next generation of discoveries in multiple myeloma. This position is ideal for an experienced computational biologist who is ready to expand into scientific product leadership without stepping away from the science, offering the opportunity to contribute to the continued evolution and development of the platform with global impact while remaining at the forefront of translational cancer research. Primary Responsibilities: Scientific Product Leadership: • Serve as the scientific product owner for the MMRF Virtual Lab and primary scientific liaison for platform users and collaborators., • Define, maintain, and execute the platform product roadmap in partnership with scientific leadership., • Translate scientific priorities into clear technical requirements and product specifications., • Prioritize new capabilities based on researcher needs, organizational objectives, and strategic opportunities., • Coordinate feature planning, testing, release management, and continuous platform improvement., • Ensure platform development consistently delivers meaningful scientific value while maintaining an exceptional user experience., • Drive long-term evolution of the platform through continuous engagement with internal and external stakeholders. Computational Biology & Scientific Innovation: • Perform computational biology and bioinformatics analyses supporting translational research initiatives., • Develop, prototype, and validate analytical workflows for future incorporation into the MMRF Virtual Lab., • Collaborate with multidisciplinary teams to translate biological questions into scalable computational solutions and platform capabilities., • Evaluate emerging computational methodologies and AI-enabled technologies for integration into future platform capabilities., • Actively participate in collaborative analyses of patient data including clinical variable, tumor cell gene expression and DNA abnormalities as well as single-cell and spatial RNA sequencing data., • Contribute to peer-reviewed publications, conference abstracts and presentations., • Support biological interpretation of complex multi-omic datasets. Scientific Leadership & External Engagement: • Support biological interpretation of complex multi-omic datasets., • Coordinate cross-functional platform development activities across scientific, engineering, and external partner teams., • Represent the MMRF and the Virtual Lab at scientific meetings, workshops, and collaborative initiatives., • Manage relationships with external software development partners, cloud providers, academic collaborators, and technology vendors to support successful platform delivery., • Develop scientific documentation, demonstrations, and educational materials supporting platform adoption and user engagement. Qualifications & Experience: Required Qualifications: • PhD in Computational Biology, Bioinformatics, Cancer Genomics, Computer Science, Biomedical Informatics, or a related quantitative discipline., • Demonstrated experience applying computational approaches to biological or clinical research., • Expertise analyzing large-scale genomic cancer datasets including tumor gene expression and DNA abnormalities and scRNAseq of tumor and the immune microenvironment., • Strong scientific publication record demonstrating contributions to computational biology, bioinformatics, genomics, or related fields., • Experience developing computational analyses, bioinformatics workflows, analytical software, or research tools., • Experience leading or coordinating multidisciplinary scientific or technical initiatives involving multiple stakeholders., • Strong understanding of modern software development practices and the ability to work effectively with software engineering teams., • Excellent written, verbal, and interpersonal communication skills, with the ability to communicate effectively across scientific, technical, and executive audiences., • Strong organizational and project management skills, with the ability to manage multiple complex initiatives simultaneously. Desired Qualifications: • Experience serving as a scientific product owner, scientific product lead, technical lead, or similar role supporting the development of research software or computational platforms., • Experience managing external software development partners, technology vendors, or multi-institution scientific collaborations., • Background in cancer genomics, precision oncology, translational research, or biomedical data science., • Experience working with cloud-based computational research environments, particularly AWS., • Familiarity with biomedical data commons, FAIR data principles, or platforms such as Gen3., • Experience developing scalable bioinformatics workflows, computational pipelines, or analytical platforms., • A passion for building innovative technologies that accelerate biomedical discovery and improve outcomes for patients. EEO Statement: The Multiple Myeloma Research Foundation (MMRF) is an equal opportunity employer and does not discriminate against any candidate based on race, religious creed, color, national origin, ancestry, physical disability, mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, age, military and veteran status, sexual orientation, or any other factor protected by federal, state, or local law. The MMRF does not sponsor/facilitate any type of work authorization for this role. All applicants must currently have original valid unrestricted authorization to accept new employment in any role in the U.S. with any employer. There is also no future employer-provided sponsorship for this role to obtain or extend authorization to work in the U.S.

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.

Founding AI Scientist - Pathology Foundation Models Remote (Must be US Based) The Role You will lead the strategy and development of pathology foundation models, shaping how they are designed, trained, evaluated, and deployed into clinical and pharmaceutical applications. This is a highly cross-functional role spanning research and production. You will define how foundation models integrate with biological context, multimodal data, and downstream decision-making systems moving beyond isolated model improvements to building end-to-end, real-world solutions. As an early-stage hire, you will play a key role in shaping both the technical direction and the organisation itself. Required Experience • Strong publication record in machine learning, including multiple first-author papers at leading conferences or journals, • Deep understanding of modern ML architectures (e.g. transformers, attention mechanisms, state-space models, mixture-of-experts), • Experience working with GPU clusters and large-scale ML infrastructure (e.g. Kubernetes, SLURM, or similar), • Solid software engineering skills and ability to build production-grade systems, • Excellent communication skills, with the ability to convey complex ideas to both technical and scientific audiences Preferred Background • Experience in oncology, cancer biology, or drug development, • Exposure to biomedical or healthcare foundation models, • Experience with multimodal and cross-modal learning systems, • Familiarity with healthcare regulatory frameworks (e.g. FDA, HIPAA), • Contributions to open-source ML ecosystems, • Experience working with distributed or community-driven research groups, • Previous experience in a startup or early-stage environment To apply please reach out to Sam Shinner at Discover International

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.

Provides technical information about wild turkey biology and management to agencies, partners, and members; contributes to Turkey Call magazine/television, the National Website, and NWTF state newsletters, webinars, and podcasts. Assists in the development and review of research project proposals fo

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

The editor will handle primarily Perspectives in biology. The editor works with the Visuals and Media teams to create striking explanatory graphics and multimedia, while ensuring excellent customer service to our authors. At least five years of experience as a commissioning editor with proven abilit

Job Type: Flexible Contract (Remote) Job Summary: We are hiring experienced clinical and research scientists, including clinical laboratory scientists, translational researchers, assay development scientists, postdoctoral researchers, and advanced doctoral candidates, for a contract project that tests whether frontier AI agents can carry out real work in clinical and translational science. You will design research-grade tasks drawn from your own laboratory practice that a leading AI model cannot solve, then review how and why the model fails. We are especially interested in scientists with hands-on flow cytometry experience in clinical or research settings. What you will do: • Design self-contained tasks drawn from the practice of clinical and translational science, such as interpreting a multi-color immunophenotyping dataset from a hematologic oncology case, gating raw FCS files to identify an abnormal cell population, evaluating whether an assay validation meets its acceptance criteria, identifying the flaw in a translational study design, and reconciling a laboratory result that conflicts with the clinical picture., • Assemble the materials each task needs, including data files, protocols, case context, and reference ranges, write a reference solution, and define clear criteria or automated checks that determine whether a solution is correct. Because laboratory data is noisy and interpretation involves judgment, criteria need to be precise or use well-justified tolerances., • Run your task against a frontier AI agent, review its attempt with the same rigor you would apply to a case sign-out or a manuscript under peer review, and refine the task until the failure reflects a real gap in the model's scientific capability rather than ambiguity or trick wording., • Work with reviewers to bring each task to acceptance. Who we are looking for: • A PhD in biochemistry, immunology, cell biology, molecular biology, pharmacology, clinical laboratory science, or a closely related field. Advanced doctoral candidates with substantial hands-on laboratory experience are also encouraged to apply., • Hands-on experience in both clinical and research settings, such as work in a CAP or CLIA-accredited laboratory alongside academic, biotech, or pharmaceutical research., • Hands-on experience in at least one of the following areas: clinical flow cytometry and immunophenotyping, assay development and validation, cell-based and immunological assays, clinical chemistry, molecular diagnostics, biomarker analysis, or translational research supporting therapeutic development., • For flow cytometry candidates: experience analyzing raw data yourself, ideally including FCS files and FlowJo or comparable analysis software, rather than only overseeing analysis., • Working knowledge of Python or R for data analysis. Familiarity with the command line and Git is a plus., • Experience in assay validation, training or mentoring other scientists, peer review, or designing course assignments and assessments is a strong advantage, because the work draws on the same skills. Why Cobalt AI: • Advance frontier AI where it counts. Apply your scientific expertise to the data that frontier labs cannot obtain any other way, where your reasoning directly shapes how the next generation of models works through clinical and experimental problems., • Grow professionally. Expand your influence through evaluation projects, advisory roles, and research collaborations, while deepening your understanding of how frontier models are trained and assessed., • Work with a top-tier network. Collaborate with scientists from leading institutions, biotech companies, and clinical laboratories on high-impact, flexible work., • Set your own schedule. Flexible 10 to 40 hour weeks that fit around your research position and your life., • Competitive pay. Rates vary by project and are determined by a number of factors, including scope, skillset, and experience.

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.

We are seeking Biology tutors and teachers in Cary.

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.

Position Summary Our partner recruitment agency specializes in early-to-growth-stage biotechnology startups to build the scientific and executive teams driving the next generation of therapeutics, platform technologies, and life science innovations. They are seeking an ambitious Scientific Recruiter holding a Ph.D. in the Life Sciences to join the team. Because clients rely on deep technical comprehension to assess key hires, your doctoral background will allow you to evaluate complex scientific capabilities, engage high-caliber research talent peer-to-peer, and act as a trusted strategic advisor to venture capital founders and startup leadership. Key Responsibilities • Technical Talent Sourcing: Leverage your scientific background to identify, engage, and recruit top-tier researchers, technical directors, and C-suite leadership for venture-backed biotech startups., • Full-Cycle Recruitment: Oversee the candidate journey end-to-end, from initial technical screening and scientific alignment through to panel interviews, offer negotiation, and placement., • Peer-to-Peer Screening: Conduct deep technical evaluations of candidate publications, research backgrounds, domain expertise (e.g., cell/gene therapy, RNA therapeutics, synthetic biology, computational biology), and cultural fit for fast-moving startup environments., • Startup Client Advisory: Work directly with biotech founders, executives, and venture partners to define headcount requirements, translate complex technical needs into compelling job profiles, and calibrate market talent availability., • Market & Scientific Intelligence: Stay current on emerging biotechnology trends, scientific breakthroughs, funding rounds, and competitive landscapes to build active talent pipelines., • ATS & Pipeline Management: Track recruitment metrics, candidate communications, and referral networks systematically within our agency ATS. Qualifications & Requirements • Education (Required): Ph.D. in Molecular Biology, Biochemistry, Biomedical Engineering, Genetics, Computational Biology, or a related Life Sciences discipline., • Industry Acumen: Understanding of early-stage biotech operations, seed-to-Series B funding dynamics, and the drug discovery/development lifecycle., • Communication & Influence: Exceptional interpersonal, oral, and written communication skills with the ability to convey complex technical concepts to non-scientific stakeholders and pitch startup opportunities persuasively., • Drive & Adaptability: High autonomy, resilience, and comfort operating in a goal-oriented, fast-paced agency environment., • Recruitment Experience (Preferred): Prior agency recruitment, executive search, or internal talent acquisition experience within life sciences is a strong plus, though post-doc or industry candidates with exceptional commercial acumen will be considered.

Drug Discovery Scientist Position: Drug Discovery Scientist Type: Hourly Contract Compensation: $60–$90/hour Location: Remote About the Opportunity This opportunity is for experienced Drug Discovery Scientists to contribute to an advanced AI research and evaluation project focused on pharmaceutical research and development. You'll apply your scientific expertise to design realistic, evidence-driven drug discovery problems that require AI models to reason through incomplete, indirect, and potentially misleading scientific evidence. You'll create research prompts, build supporting data rooms using real source-grounded information, develop rigorous grading frameworks, and validate the resulting tasks. The role is ideal for experts who can distinguish genuine scientific reasoning from pattern matching and confidently evaluate the quality of complex research conclusions. Responsibilities • Design challenging, realistic drug discovery research problems based on authentic scientific workflows., • Develop research scenarios where the correct conclusion must be derived from multiple pieces of evidence rather than directly stated., • Build comprehensive data rooms using real, source-grounded scientific data and documentation., • Ensure every decisive scientific value and piece of evidence can be traced back to a reliable source., • Create detailed grading documents and evaluation rubrics that assess scientific reasoning and substantive conclusions., • Evaluate AI-generated research outputs for scientific accuracy, logical consistency, and defensibility., • Run verification and calibration processes to ensure tasks are reproducible, appropriately difficult, and objectively scorable., • Identify weaknesses in task design, evidence, or evaluation criteria and revise them accordingly., • Provide expert judgment on scientific questions, task difficulty, and the quality of AI reasoning., • Collaborate with project reviewers and other domain experts to refine research tasks. Required Qualifications • Professional expertise in one or more of the following areas:, • Mechanistic enzymology, • Structure-guided peptide design, • Structure-guided antibody design, • Fragment-based drug discovery, • Structure-based medicinal chemistry, • PhD or equivalent industry experience in drug discovery, medicinal chemistry, chemical biology, biochemistry, or a closely related field., • Strong understanding of drug discovery research methodologies and scientific evidence evaluation., • Ability to construct complex scientific problems with defensible conclusions., • Strong analytical and critical-thinking skills., • Ability to evaluate scientific reasoning quality, not simply final answers., • Strong scientific writing and documentation skills., • Comfortable working independently in a remote research environment., • Ability to commit at least 20 hours per week. Preferred Qualifications • Experience designing or evaluating drug discovery research strategies., • Strong background in structure-based drug design, protein–ligand interactions, enzymology, or molecular discovery., • Experience working with scientific literature, experimental datasets, structural data, and research documentation., • Experience developing research assessments, scientific benchmarks, or evaluation frameworks., • Familiarity with open-source scientific tooling and computational research workflows., • Experience evaluating AI-generated scientific research or technical outputs is a plus., • Strong ability to distinguish defensible scientific conclusions from unsupported assumptions or superficial reasoning. Compensation • Competitive compensation of $60–$90/hour., • Hourly contract engagement., • Fully remote., • Minimum commitment: 20 hours/week., • Up to 40 hours/week available., • Claude Max subscription required for the project and fully reimbursed., • Work conducted through a browser-based research studio and Claude Code. Application Process • Apply to the role, • Complete the required screening questions, • Provide details about your drug discovery and scientific research experience, • Complete the relevant scientific assessment, • Participate in the evaluation/interview stage, • Complete onboarding and tooling setup, • Begin designing and evaluating drug discovery research tasks

Courses: Life Science, Physical Science and Earth & Space Science (grades 5–8), Biology (grade 9) and Chemistry (grade 10). In the first line of your application, please state the role (Math, ELA or Science), the US state you live in, and the state that issued your teaching license. Maevious, a li

Advanced degree in biology, immunology, cell biology, biochemistry, or a closely related life sciences field. 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 e

Who are we? At Bioz, we are transforming how scientists discover, evaluate, and select the products and services that power breakthrough research. Our AI-driven platform replaces slow, manual scientific search with precise, data-backed insights drawn from tens of millions of scientific publications. Built for researchers and the companies that support them, Bioz has become a trusted platform for scientific product discovery, validation, and engagement. By combining deep chemical and biological entity recognition, sentiment analysis, and patented AI technology, Bioz helps scientists make faster, more confident decisions while enabling suppliers of scientific research products to showcase real-world product usage, validation, and credibility at scale. We are looking for a Senior Business Development Representative who brings energy, discipline, curiosity, and a strong desire to win. This role is ideal for someone who thrives in a fast-paced, AI-enabled sales environment, takes pride in sharpening their outbound craft, and wants to help scale a platform that is actively accelerating global scientific discovery. What will you accomplish? • Generate qualified new business opportunities across global markets through strategic outbound prospecting, including email sequences, LinkedIn outreach, cold calling, trade shows, and other targeted channels., • Identify, prioritize, and nurture high-potential prospects within companies that supply scientific research products and services., • Understand each prospect’s business needs, challenges, and goals, and clearly communicate relevant insights to the Bioz Account Executives you partner with., • Articulate Bioz’s value proposition, AI capabilities, badges, and data solutions in a compelling way that aligns with each prospect’s specific priorities and pain points., • Maintain accurate, timely, and detailed records of prospect interactions, account insights, and next steps in the CRM., • Collaborate closely with sales, marketing, and product teams to share market feedback, improve outbound processes, and contribute to ongoing product and positioning improvements. What do we need from you? • 1+ years of experience in B2B technology prospecting, preferably in an SDR, BDR, or similar outbound prospecting role., • Proven experience building pipeline through cold calling, email outreach, LinkedIn prospecting, and other outbound sales motions., • Excellent written and verbal communication skills in English, with the ability to engage prospects clearly, confidently, and professionally. Additional language proficiency is a plus., • A collaborative mindset and openness to giving and receiving feedback as part of a team committed to improving sales and marketing processes., • High energy, resilience, curiosity, and a strong desire to continuously learn, improve, and win., • A reliable remote work setup and the discipline, accountability, and communication skills needed to thrive in a fully remote environment. What would give you an edge? • 1+ years of B2B SaaS prospecting experience, ideally in a fast-paced, outbound-focused environment., • Domain experience or an educational background in science, biotech, biology, chemistry, or a related field., • Hands-on experience with HubSpot, Apollo, LinkedIn Sales Navigator, or other CRM and sales engagement platforms., • A proven track record of exceeding quota as an SDR, BDR, or similar sales development role in a SaaS environment. What's in it for you? • Trade show opportunities: Represent Bioz at industry trade shows across the U.S., with potential opportunities to attend international events in Europe, Japan, and other key markets., • Fully remote work environment: Enjoy the flexibility to work from where you are most productive, while collaborating with a distributed, high-performing team., • Top-spec hardware: Receive a high-performance laptop and the tools you need to do your best work from day one.

Work Arrangement: Regular Location: Raleigh, NC, US, 27617 Personnel Area: DUKE HEALTH INTEGRATED PRACTIC Date: Sep 15, 2026 JOB LOCATION Duke GI-Endoscopy at Brier Creek - 10207 Cerny St JOB SUMMARY We are seeking a Clinical Operations Supervisor to directly supervise Endoscopy Surgical Technologists, Patient Care Technicians and a Supply Chain Associate's during specified shifts, facilitating staff and departmental efficiencies while monitoring the clinic's daily operations to ensure that appropriate quality and productivity levels are achieved and the appropriate supplies and equipment are ordered and maintained. Ensures compliance with infection control policies and AAMI, AORN, and Joint Commission standards. Assures compliance with infection control, sterilization and high level disinfection standards, ensuring that sterilization and high level disinfection practices and all equipment used for decontamination and sterilization meet quality standards. Assists staff with performance improvement. Supervisory responsibilities include staff selection, orientation/onboarding, performance evaluation, counseling, and staff development. JOB DUTIES AND RESPONSIBILITIES Schedules and supervises the work of assigned staff to ensure smooth workflow in the department. Schedules staff in accordance with department needs. Acts as a knowledge resource to staff in matters of department processes, technical skills, equipment, supplies and/or regulatory requirements. Selects, trains, and manages the performance of staff. Provides daily direction to staff. Sets goals for individuals and for the team. Acts as a mentor and coach and provides development and growth opportunities for staff. Coordinate and maintain departmental workflow in decontamination, the inspection of instruments/trays, cleaning, assembling, and packaging of surgical instruments, medical/surgical materials/supplies, and equipment. Monitors inventory of supplies and equipment. Coordinate procurement and stocking activities. Analyze usage patterns of supplies and recommend optimal par levels. Assists in developing goals, targets, and action plans. Facilitates the timely ordering of instrumentation and supplies. Identifies opportunities for cost reduction and expense control. Provides management with information for forecasting future instrumentation/equipment needs. Track and document lost or damaged equipment and supplies. Identifies opportunities to improve work processes and enables achievement of goals in quality, productivity, and customer satisfaction. Provides a forum for staff involvement in problem identification and resolution. Develops and implements solutions to address opportunities to improve quality, safety, efficiency, and productivity. Oversight for the cleaning, decontamination, assembly, maintenance, and preventative maintenance, and high-level disinfection of all reusable medical instrumentation. Participate in the cleaning, decontamination, assembly, and disinfection of scope trays and equipment following established tray lists and manufacturer's recommendations as needed. JOB ELIGIBILITY REQUIREMENTS Work requires a bachelor's degree in biology, physiology, psychology, or a related scientific field. Three to four years of clinical technical experience to gain expertise in the principles, theories, procedures, and equipment in the Endoscopy field. Prefer high-level disinfection experience and supervisory experience. Current certification as a Sterile Processing Technician through an accredited organization (CRCST - Certified Registered Central Service Tech, HSPA, or Certified Sterile Processing and Distribution Technician CBSPD). Good customer service skills Ability to understand and follow oral and written instructions. Working knowledge of sterile techniques, infection control procedures, and safety precautions applicable to work performed. Ability to establish and maintain effective working relationships with patients and clinic staff. Customer service skills. Ability to maintain inventory, attention to detail, and organizational skills. JOB HOURS The schedule for this position is day shifts, Monday-Friday, with no weekends or holidays. Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy related conditions), sexual orientation or military status. Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideasan exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of our community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values. Essential Physical Job Functions: Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and provision for requests for reasonable accommodation will be provided by each hiring department.

A rapidly growing and innovative life sciences organization is seeking a motivated Sales Representative to support business development and customer growth throughout the Southeast United States. This is an exceptional opportunity for a recent college graduate or early-career professional with a background in life sciences who is interested in building a career in technical and consultative sales. Previous sales experience is helpful, but not required. We are looking for someone who is curious, driven, highly motivated, and excited to develop relationships while learning the science and technology behind innovative laboratory and bioprocess solutions. Through a structured graduate sales program, you will receive training, coaching, and hands-on experience while working with pharmaceutical, biotechnology, CDMO, research, and laboratory organizations. • Participate in a comprehensive training and development program designed to build technical sales and business development skills., • Develop and execute a territory growth strategy across the Southeast U.S., • Prospect for new business and develop relationships with prospective customers., • Build trusted customer relationships through consultative, solution-focused selling., • Learn and communicate technical information related to laboratory and bioprocess products., • Support existing customer accounts while identifying opportunities for additional products and solutions., • Conduct customer presentations, product discussions, and sales meetings., • Collaborate with internal product, engineering, technical, and customer support teams to deliver strong customer experiences., • Identify new market opportunities and share customer insights with internal teams., • Manage sales activities, customer interactions, pipeline development, and opportunities through CRM., • Work toward achieving and exceeding territory sales objectives., • Develop the knowledge, relationships, and sales skills necessary for long-term career growth within the organization., • Bachelor's degree in Life Sciences, Biology, Chemistry, Biochemistry, Biomedical Sciences, or a related scientific field preferred., • Recent graduates and early-career professionals are encouraged to apply., • Previous sales, customer-facing, laboratory, research, or industry experience is a plus but not required., • Strong interest in developing a career in technical sales, business development, and account management., • Ability to learn and communicate scientific and technical information effectively., • Strong communication, presentation, organization, and relationship-building skills., • Comfortable initiating conversations, prospecting for new business, and developing customer relationships., • Self-motivated, competitive, curious, and willing to learn., • Ability to work independently while collaborating effectively with internal teams., • Comfortable using CRM software and other business tools, or willing to learn., • Strong time-management skills and the ability to manage multiple priorities across a large territory., • Willingness to travel approximately 5055% throughout the Southeast., • Biopharmaceutical manufacturing, • Biotechnology, • Pharmaceutical manufacturing, • Laboratory products or equipment, • Bioprocessing, • CDMOs & CMOs, • Cell & gene therapy, • Vaccine manufacturing, • Research laboratories, • Process development, • Manufacturing operations, • Join a financially strong, growth-focused organization investing in innovation., • Launch your career through a dedicated graduate sales development program., • Receive training, coaching, and mentorship from experienced sales and industry professionals., • Develop valuable expertise at the intersection of science, technology, and sales., • Represent innovative products and solutions within the growing life sciences industry., • Build relationships with leading pharmaceutical, biotechnology, CDMO, and research organizations., • Enjoy a high degree of autonomy while receiving strong leadership and team support., • Competitive base salary, uncapped incentive opportunity, comprehensive benefits, and long-term career advancement., • Significant opportunity to grow professionally as the territory and organization expand. You don't need years of sales experience to succeed in this role. We're looking for potential. If you have a scientific or life sciences background, enjoy meeting and learning from people, are motivated by goals, and want to develop a career where science meets sales, this could be an excellent opportunity to launch your career. Recent graduates and early-career professionals with a strong interest in life sciences sales are encouraged to apply.

At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advance health together. Pursue your passion for caring with Duke Health Integrated Practice, which comprises more than 110 primary and specialty outpatient clinics, extending the reach of Duke Health's mission across the state of North Carolina. Job Location: Duke GI-Endoscopy at Brier Creek - 10207 Cerny St Job Summary: We are seeking a Clinical Operations Supervisor to directly supervise Endoscopy Surgical Technologists, Patient Care Technicians and a Supply Chain Associate's during specified shifts, facilitating staff and departmental efficiencies while monitoring the clinic's daily operations to ensure that appropriate quality and productivity levels are achieved and the appropriate supplies and equipment are ordered and maintained. Ensures compliance with infection control policies and AAMI, AORN, and Joint Commission standards. Assures compliance with infection control, sterilization and high level disinfection standards, ensuring that sterilization and high level disinfection practices and all equipment used for decontamination and sterilization meet quality standards. Assists staff with performance improvement. Supervisory responsibilities include staff selection, orientation/onboarding, performance evaluation, counseling, and staff development. Job Duties and Responsibilities: • Schedules and supervises the work of assigned staff to ensure smooth workflow in the department. Schedules staff in accordance with department needs. Acts as a knowledge resource to staff in matters of department processes, technical skills, equipment, supplies and/or regulatory requirements., • Selects, trains, and manages the performance of staff. Provides daily direction to staff. Sets goals for individuals and for the team. Acts as a mentor and coach and provides development and growth opportunities for staff., • Coordinate and maintain departmental workflow in decontamination, the inspection of instruments/trays, cleaning, assembling, and packaging of surgical instruments, medical/surgical materials/supplies, and equipment., • Monitors inventory of supplies and equipment. Coordinate procurement and stocking activities. Analyze usage patterns of supplies and recommend optimal par levels. Assists in developing goals, targets, and action plans., • Facilitates the timely ordering of instrumentation and supplies. Identifies opportunities for cost reduction and expense control. Provides management with information for forecasting future instrumentation/equipment needs. Track and document lost or damaged equipment and supplies., • Identifies opportunities to improve work processes and enables achievement of goals in quality, productivity, and customer satisfaction. Provides a forum for staff involvement in problem identification and resolution. Develops and implements solutions to address opportunities to improve quality, safety, efficiency, and productivity., • Oversight for the cleaning, decontamination, assembly, maintenance, and preventative maintenance, and high-level disinfection of all reusable medical instrumentation., • Participate in the cleaning, decontamination, assembly, and disinfection of scope trays and equipment following established tray lists and manufacturer's recommendations as needed. Job Eligibility Requirements: • Work requires a bachelor's degree in biology, physiology, psychology, or a related scientific field., • Three to four years of clinical technical experience to gain expertise in the principles, theories, procedures, and equipment in the Endoscopy field., • Prefer high-level disinfection experience and supervisory experience., • Current certification as a Sterile Processing Technician through an accredited organization (CRCST - Certified Registered Central Service Tech, HSPA, or Certified Sterile Processing and Distribution Technician CBSPD)., • Good customer service skills, • Ability to understand and follow oral and written instructions., • Working knowledge of sterile techniques, infection control procedures, and safety precautions applicable to work performed., • Ability to establish and maintain effective working relationships with patients and clinic staff., • Customer service skills., • Ability to maintain inventory, attention to detail, and organizational skills. Job Hours: The schedule for this position is day shifts, Monday-Friday, with no weekends or holidays. Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy related conditions), sexual orientation or military status. Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideasan exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.

🌎 District Sales Manager — Analytical Instrumentation 📍 Based in the Raleigh, NC, area | Regional Travel Required 🏢 Swan Analytical USA 🕒 Full-Time | Entry to Mid-Level Drive Growth. Build Relationships. Make an Impact. Swan Analytical USA is a global leader in high-precision water analysis instrumentation, and we’re looking for a District Sales Manager to join our team. This is an exciting opportunity for a technically minded sales professional who thrives at the intersection of science and business — someone who enjoys connecting technology with customer needs to deliver real-world value. What You’ll Do • Develop and execute regional sales strategies to exceed growth targets., • Build and manage a healthy sales pipeline through proactive outreach and relationship building., • Identify and convert new business opportunities while supporting existing accounts., • Collaborate with technical experts to deliver engaging demos and solutions., • Prepare persuasive presentations and proposals for customers and partners., • Negotiate contracts with a focus on mutual success., • Report on sales performance, market insights, and customer feedback., • Represent Swan Analytical at trade shows, conferences, and industry events. 🗓️ A typical week includes office days on Mondays and Fridays at your home, with most regional travel occurring from Tuesday through Thursday. What You Bring • Bachelor’s degree in Chemistry, Engineering, Biology, or related field (preferred)., • Sales experience in analytical instrumentation, water analysis, or other technical fields is a bonus., • Previous experience in water treatment, wastewater treatment, and power plant chemistry (preferred), • Excellent communication, presentation, and negotiation skills., • Self-motivated, organized, and results-oriented mindset., • Proficiency with CRM tools and Microsoft Office Suite., • Valid driver’s license and willingness to travel regionally. Why You’ll Love Working Here • 💰 Competitive base salary + commission structure, • 🎓 Comprehensive training and ongoing professional development, • 🌱 Career growth opportunities within a global organization, • 🤝 Supportive, collaborative team culture, • 🌍 Meaningful work — contribute to cleaner, safer water worldwide Ready to Take the Next Step? If you’re passionate about science, sales, and building lasting customer relationships — we’d love to meet you. 📩 Apply now or reach out directly to learn more about joining the Swan Analytical team.

Job DescriptionAre you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn. This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, 1st Edition Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs)., • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical submission documents for INDs/CTAs/NDAs/BLAs/MAAs, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity., • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data., • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents., • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports)., • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC., • Demonstrated ability to lead others to complete complex projects., • Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines., • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment., • Organizational expert within the nonclinical subject area., • Excellent written/oral communication and strong time and project management skills., • Ability to attend regular team meetings, lead client meeting and CRMs., • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars., • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP). Requirements: • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control., • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements., • 5+ years of pharmaceutical regulatory nonclinical writing experience., • Strong writing and analytical skills., • Proficiency with MS Office applications., • Hands-on experience with clinical trial and pharmaceutical development preferred., • Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process. Powered by JazzHR 7RZuzwxKjI

At least 3 years of professional experience in fields such as Cell Biology, Molecular Biology, Genetics & Genomics, Physiology, Ecology, Evolutionary Biology, Microbiology, Immunology, Biochemistry, Developmental Biology, Biotechnology, Bioinformatics & Computational Biology, Biomedical Sciences, Ag

Adjunct Instructor, Department of BiologyWilliam Peace University is continuously seeking qualified scholars for adjunct faculty positions in the Biology department who have demonstrated commitment to the promotion of interdisciplinary work, teaching excellence, diversity, and possess a collaborativ

Job Description Invaluable experience for aspiring Pre-PA, Nursing and Medical School Candidates. You have the chance to be a part of a clinical team while always being at the right hand of the physician. IMPORTANT: It is helpful for student candidates to stack classes to be able to work a weekday day shift schedule. Part-time and full-time opportunities are available. Medical Scribe Position MedScribes seeks highly motivated, customer service oriented candidates interested in a health care opportunity to work directly with physicians, patients and the clinical care team. This is a non-clinical role, for which on-site training is provided and certification is NOT required. A scribe will observe physician-patient interactions to provide real time clinical documentation in and around the Triangle area of North Carolina. Site placement is based on a strong match of client needs and staff availability to meet the goal of creating a winning partnership. Benefits to our Scribes: • Dedicated on-site training tailored to support a strong foundation for success, • Master the use of the electronic health record, medical terminology and clinical documentation through consistent shift work., • Integration on to a clinical team for direct exposure to patient-provider interactions., • Work with multiple providers within a specialty to gain breadth and depth, • Gain perspective for clinical decision making, clinical workflow, team dynamics, • Build relationships with clinicians that offer mentorship and letters of recommendation, • Connect with peers on a similar career path., • Flexible scheduling to manage classes and work, • Test prep and scrubs attire discounts, • Leadership opportunities are available Requirements for all scribe openings: • Minimum Age: 19 years old, • Commitment: Minimum 2-3 shifts per week, about 20 hours per week for 1 year, • Transportation: Valid driver’s license and reliable transportation required., • Typing skills: Minimum 60 words per minute., • Education: College-level biology, anatomy, and/or medical terminology preferred., • Experience: Exposure to clinical environment preferred, but not required., • Personality: Motivated, eager to learn, customer-oriented, flexible. Typical clinic schedule. Candidates should be available to work some weekdays: • Clinic opportunities - week day schedule with start times at 7a - 5pm, with prep time from home that is paid time. Note: These are examples and the specific schedule may vary slightly by specific department or site set up. #medscribes