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Job Description Job Title: Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance / Regulatory Affairs Employment Type: Monday - Friday 8:30am - 5pm $20/ HR We are currently seeking a Quality Control Document Specialist with a strong background in microbiology to support our Quality Control Department. This position plays a key role in ensuring compliance with regulatory standards and maintaining a clean, safe, and efficient laboratory environment. MUST BE BILINGUAL ENGLISH/SPANISH Minimum Qualifications: • Bachelor’s degree in Microbiology, Biology, Biomedical Science, or a related field required; Master’s degree preferred, • Minimum of 1 year of experience in a microbiology laboratory within a cGMP-regulated manufacturing environment, • Solid understanding of microbial techniques and methodologies to monitor bacteria, fungi, and other microorganisms, • Follow all procedures and processes to ensure compliance with current Good Manufacturing Practices (cGMP), • Conduct daily monitoring of microbial cultures in the microbiology laboratory, • Perform laboratory testing and analyses as assigned, including testing of raw materials, finished products, and water samples, • Review analytical assay data for accuracy and compliance; determine acceptability of results, • Inspect manufacturing equipment and personnel for potential sources of contamination, • Support root cause analysis and investigations for out-of-specification (OOS) results, • Maintain clear, organized, and accurate documentation of lab procedures and test results, • Ensure that all work meets established timelines and client or regulatory requirements, • Collaborate with other departments to identify and resolve technical issues, • Contribute to the development and maintenance of safety and compliance standards within the lab, • Strong attention to detail and documentation accuracy, • Effective communication and collaboration skills, • Ability to work independently and prioritize tasks in a fast-paced environment, • Proficient in Microsoft Office and laboratory data systems

Advance your career with Mindlance! We have been connecting talented professionals with world-class companies since 1999. Mindlance is here to help you to find the perfect fit with just the right company. Currently, we are seeking a Histotechnician I for an exciting career growth opportunity. Make your next big career move with the kind of position that will allow you to be genuinely passionate about the work you do! Our recruiters and team will work closely with you to help you get the edge over the competition. Let Mindlance advocate for you – apply today! Job Title: Histotechnologist I. Job Location: Pompano Beach FL 33069 Pay Rate Range: $42/hr. to $55/hr. on W2. Duration: 3+ months (As of now it is only a Temp assignment for 04 Plus months and will be hired full time perm too.) 40 hours a week. Weekdays. Opening 1) 5:00 AM to 1:30 PM (Early morning) Opening 2) 8:00 PM to 4:30 AM (Night) *Must have Florida CLP license and ASCP HT or HLT certification Duties: • Perform routine and non-routine activities involved in the preparation of slides for microscopic evaluation by pathologist(s), according to policies and procedures., • Capable of performing all of the duties/responsibilities of a Histotechnician I and II., • Ensure proper accessioning and labeling of all tissue samples., • Process paperwork associated with accessioning and reporting., • Ensure proper tissue processing., • Embed processed tissue in paraffin., • Perform microtomy of embedded tissue., • Prepare slides for routine Hematoxylin and Eosin staining., • Perform coverslipping of stained slides either manually or automated., • Prepare solutions and reagents for special stain procedures., • Obtain and validate tissue used in special stains., • Perform all special stain procedures., • May prepare solutions and reagents for IHC procedures., • May obtain and validate control material used in IHC procedures., • May perform IHC testing. Perform filing of finished blocks and slides., • Perform routine maintenance and cleaning of equipment and troubleshoot minor equipment failures., • Document remedial actions such as repairs or repeated tests., • Provide training and guidance to Histotechnicians, students and lab aides., • Adhere to laboratoryýýs quality control policies and document all quality control activities., • Ensure all corporate safety, quality control and quality assurance standards are met., • Ensure compliance with all local, federal, CLIA and CAP regulations., • Maintain a clean and well-organized work area., • Other duties, as assigned by supervisor., • BS, ASCP HT Required Work Experience: • 1 year Previous histotech background required., • Routine embedding and microtomy needed., • Must have Florida CLP license and ASCP HT or HLT certification Education: BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990. Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). United States educated candidates must provide a detailed original transcript. EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

Our client is dedicated to providing innovative and affordable solutions for healthier lives. Our ultimate goal is to provide innovative and affordable solutions to help the millions of people living with diabetes enjoy a better quality of life. We have become a leading developer, manufacturer and marketer of advanced performance products including a broad portfolio of blood glucose monitoring supplies and technologies. We currently seek a Senior Director of Regulatory Affairs to support the strategic direction and lead the day-to-day execution of global regulatory activities. This role will be responsible for preparing high-quality regulatory submissions, supporting interactions with the FDA and other international regulatory bodies, and ensuring compliance with global requirements related to market authorizations, post-market surveillance, and regulatory reporting. SCOPE OF WORK SUMMARY • Be responsible for all matters related to regulatory affairs and FDA compliance., • Coordinate and facilitate US regulatory submissions and international (Outside US or OUS) regulatory registrations., • File for and maintain CLIA waivers when needed., • Approve product labeling, ensuring compliance with requirements., • Participate in review, approval, and implementation of product changes., • Provide guidance on regulatory requirements for business partners and internal customers., • Provides advice and strategy planning with regards to compliance issues related to the FDA and OUS regulatory requirements, particularly in the USA, UK, EU, Canada, Mexico, Brazil, Australia, and Japan., • Be responsible for US Medical Device Reporting and global vigilance reporting., • Serve as European Person Responsible for Regulatory Compliance., • Collaborate to support inter-company projects, • Provide guidance on regulatory requirements for business partners and internal customers. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. • This is an on-site position. Remote work is not suitable for this position., • Write, update, and file US regulatory submissions including 510(k)’s, CLIA submissions and FDA correspondence relating to issues as required, • File and update international regulatory submissions and product registrations/licensing, • Develop the timeline for US-FDA and international submissions based on the marketing and sales strategic plans, • Work with colleagues to outline data submission requirements as required, • As part of the Project Team, coordinate the collection of technical data to support submissions, • Provide global regulatory strategies for new and modified products, • Provide guidance on regulatory requirements for business partners and internal customers, • Interface with executive management regarding applicable regulations and ensure regulatory compliance, • Interface with all functional areas to advise on and assist with any compliance matters, • Provide direction and guidance in the interpretation of the FDA Medical Device Reporting, UKCA, EU Medical Device Vigilance Reporting (and other markets as required) related to product incidents and potential adverse events, • Company representative for all product/quality system regulatory agencies and Ministries of Health, to include FDA, European Notified Body, UKCA, ISO Registrar and Competent Authorities of the European Union. Remain current on regulatory requirements within these main markets., • Maintain product technical files / technical documentation / declarations of conformity as required within the EU, UK, Australia, etc., • Maintain registrations in foreign countries and ensure that shipments of products are not sent to non-registered countries., • Company representative for all quality system auditors regarding regulatory affairs compliance, • Adhere to all workplace safety laws, regulations, standards and practices, • Remain current and compliant with all training requirements, • Oversee the Customer Care functions responsible for monitoring and managing the daily activities of end user complaint handling for fielded products., • Note – this position is not responsible for compliance with import/export laws, tariffs, patents, intellectual property, REACH, RoHs, or fraud/abuse laws. SUPERVISORY RESPONSIBILITY • Manage subordinate supervisors and employees in Regulatory Affairs and Customer Care, • Be responsible for the overall direction, coordination, and evaluation of this functional area, • Carry out supervisory responsibilities in accordance with organization's policies and applicable laws, • Be responsible for interviewing, hiring, and training employees in regulatory affairs, • Plan, assign, and direct work, • Appraise performance, reward and discipline employees, • Addressing complaints and resolving problems EDUCATION and/or EXPERIENCE • Bachelor of Science in Chemistry, Biology, Medical Technology, Engineering, or related area from an accredited four-year college or university, • Fifteen years related experience with in vitro diagnostics (IVDs) or equivalent combination of education and experience. Experience with medical devices may be able to substitute for some of the qualifications., • Clinical laboratory experience highly desired., • RAC certification preferred, • Strong scientifically based background MATHEMATICAL SKILLS • Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. While this level may not be required, it is desirable when reviewing scientific documents from the R&D group. The ability to understand the concepts is more valuable than the application. LANGUAGE SKILLS • Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents., • Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community., • Ability to write speeches and articles for publication that conform to prescribed style and format., • Ability to effectively present information to senior management, and/or public groups. Because there is no higher local regulatory position in this company, level and skills exceeding the above may be required from time to time. REASONING ABILITY • Ability to define problems, collect data, establish facts, and draw valid conclusions, • Ability to interpret an extensive variety of technical instructions in mathematicalor diagram form and deal with several abstract and concrete variables, • Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems, • Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.,) in its most difficult phases, • Ability to deal with a variety of abstract and concrete variables, • Again, not required but desirable because this knowledge assists with review of both internal and external technical documentation.

Post-Doctoral Research Associate Location: Fort Lauderdale-Davie, FL Salary: $51,500 Category: Exempt | Full-time | 3-year grant funding availability About the Role Nova Southeastern University is seeking a Post-Doctoral Research Associate to join our innovative research team advancing cancer biology and immuno-oncology. In this role, you will work closely with senior faculty and research personnel, contributing as a skilled researcher on projects focused on in vivo and in vitro characterization of novel anti-melanoma leads. This position is ideal for early-career scientists eager to deepen their expertise, publish impactful findings, and collaborate on cutting-edge studies that have the potential to shape the future of cancer therapeutics. Key Responsibilities • Conduct high-level independent and collaborative research in cancer biology and immunotherapy., • Design and apply scientific and numerical models; develop protocols and instrumentation for data collection., • Perform and oversee laboratory experiments, including advanced techniques and procedures involving radioactive materials., • Analyze data and contribute to manuscripts, abstracts, and publications; present findings at professional meetings., • Collaborate with senior researchers on long-term research strategies and grant initiatives., • Provide guidance to junior researchers, staff, or fellows, supporting the daily operations of the lab., • Contribute to committees, program development, and curriculum enrichment where appropriate. Qualifications Required Education & Experience: • Doctoral or terminal degree in Biochemistry, Cancer Biology/Immunology, Molecular Biology, Pharmacology, Cell Biology, or a related field., • 0–2 years of experience in an academic or laboratory research environment., • Previous research experience in immune-oncology or cancer immunotherapy. Preferred Experience: • Background in melanoma biology., • Experience with spatial proteomics/transcriptomics., • Hands-on experience with in vivo studies. Skills & Competencies • Strong knowledge of chemistry, mathematics, and scientific methodology., • Proficient in critical thinking, complex problem solving, and advanced research analysis., • Excellent written and verbal communication skills for collaboration and publication., • Ability to manage multiple research initiatives and ensure the integrity of data collection. Why Join NSU? As a Post Doctoral Research Associate at Nova Southeastern University, you’ll join a collaborative and forward-thinking research environment dedicated to innovation and discovery. With access to advanced facilities and opportunities to publish and present, this role will allow you to grow as a scientist while contributing to the fight against cancer. Apply today to be part of groundbreaking cancer research and help drive the next generation of discoveries.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Business Unit Manager (BUMa) is responsible for maintaining positive operating margin at the laboratory level and for meeting and exceeding the annual budget. Supervises all laboratory personnel and provides leadership and direction as needed. Responsible for ensuring compliance and integration of facility operation with corporate and regulatory policies and procedures. The Business Unit Manager will serve as a liaison with corporate business partners and will champion Company policies, vision, and mission. Business Unit Manager responsibilities include, but are not limited to, the following: · Lead team, schedule, and train employees · Ensure adherence to highest quality and efficiency standards in laboratory operations · Ensure coverage and performance · Foster morale and teamwork · Demonstrates and promotes the company vision · Regular attendance and punctuality · Manage the technical conduct, quality control, and related record keeping of all analytical evaluations performed · Responsible for the supervision, organization, and coordination of all technical activities of personnel within the principles of sound scientific endeavors, business economy, and the professional development of subordinate employees. · Provide the necessary planning, organization, direction, and control to meet the goals of the company. · Ensure that all pertinent company health, safety, and environmental programs are adhered to and documentation is maintained. · Establish and maintain professional business relationships with clients, industry officials, and peers. · Assist in the generation of marketing strategies, prepare comprehensive technical work proposals, and maintain an influential position in establishing business expansion plans. · Provide input toward the financial growth and development of the company. · Coordinate business activities with the Business Unit Managers from the other locations to ensure customer expectations are met without duplication of testing activities. · Responsible for the overall operational success of the laboratory, which includes, but is not limited to: budgeting, making decisions on capital expenses, managing senior staff, attending to major client needs, revenue & profit growth, and cost control. · Oversee daily operations including: laboratory, quality, logistic, and managerial duties. · Represent the laboratory in technical meetings. · Participate with the Sales/Marketing team in the preparation and quotation of major technical studies. · Propose major investments to company executives. · Ensure that the laboratory expenses are on track with the annual budget. · Approve major expenses and control the costs of the laboratory within established company guidelines. · Analyze monthly laboratory indicators (operating and labor costs, turnaround time, productivity, etc.). · Verify that company employment policies and procedures are followed correctly. · Perform annual performance reviews for direct reporting personnel. Coordinate and review annual reviews of other lab personnel. · Handle employee relation issues as per company guidelines and with the support of Human Resources. · Coordinate the interaction between the different laboratory departments. · Understand and follow each Quality System document relevant to employment responsibilities, e.g., methods, SOPs, etc. Propose changes to documents and approve documents when required · Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Education: · Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) · MS Experience: · At least 10 years of supervisory experience · At least 10 years professional experience in laboratory operations with a minimum of 5 years of laboratory operations or large/multi-department/team leadership with profit/loss accountability - $5M+ Net Sales or equivalent size operation. Demonstrated success in improving operational, profit, quality and safety performance. · Familiarity with laboratory operations and services · Familiarity with EPA, DOT, OSHA, and DOL regulations · Excellent verbal and written skills · Strong customer relations skills · Ability to manage a business at a profit/loss responsibility level · Ability to control operating budgets · Ability to develop and enforce policies and operating practices · Ability to prioritize and delegate responsibilities · Ability to successfully handle contract and other negotiations · Strong decision-making abilities · Problem-solving abilities Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Additional Information We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years. We do not offer Visa Sponsorship for this role. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Are you a passionate Research Scientist with a background in hematology and regenerative medicine? Do you want to take your career to the next level in a fast-paced and innovative environment? Biofyl Scientific Research, a leader in regenerative medicine for over 20 years, is seeking a talented and driven scientist to join our team. We specialize in hematology and autologous biologics research, providing expert scientific services for regulatory, marketing, and R&D purposes. If you are a technical expert who thrives on high-level lab work and enjoys method development, we want to hear from you. This is a unique opportunity that requires relocation to the Fort Myers, Florida area. Qualified applicants will receive a signing bonus after a probationary period. What You'll Do: Key Responsibilities: As a key member of our laboratory team, you will play a crucial role in the execution of our research projects and daily operations. Your expertise will be essential in: • Handling and Analyzing Samples: You will work extensively with blood and bone marrow samples, performing advanced lab techniques such as Optical aggregometry, ELISA, Flow cytometry, Cell culture, and Microscopy., • Conducting and Managing Research: Efficiently perform investigational studies following established SOPs while ensuring the accuracy of all test results before reporting., • Maintaining Lab Excellence: Contribute to the day-to-day operations of the lab, including instrument maintenance, quality control, method setup, and troubleshooting. Non-Negotiable Qualifications: • A Bachelor of Science degree in Biotechnology, Cell Biology, Molecular Biology, or a closely related field., • A minimum of two years of hands-on experience in a lab scientist or similar role., • A Master's or Ph.D. in a relevant field.

Job Description Who we are: Cosmetic Solutions is a leader in the development and manufacturing of scientifically proven, innovative personal care products. With a focus on, face, body, hair, OTC, and professional use formulations, we create some of the most cost effective, high quality and powerful products on the market. Providing world class services to up and coming businesses, large established brands, physicians, estheticians and other skin care professionals; we specialize in research & development, custom formulization, graphic design, manufacturing, packaging and delivery. Job Title: Quality Assurance Specialist Company Overview: We are a leading manufacturing company dedicated to delivering high-quality products to our customers. Our commitment to excellence drives everything we do, and we are seeking a Quality Assurance Specialist to join our team and uphold our standards of quality and compliance. Position Overview: As a Quality Assurance Specialist, you will play a critical role in ensuring that our manufacturing processes meet regulatory requirements and adhere to our company's quality standards. You will be responsible for overseeing various aspects of quality assurance, including Good Manufacturing Practices (GMP), quality systems, Corrective and Preventive Actions (CAPAs), deviations, document control, and Standard Operating Procedures (SOPs). Key Responsibilities: • Good Manufacturing Practices (GMP):, • Ensure compliance with GMP regulations throughout the manufacturing process., • Conduct regular audits and inspections to verify adherence to GMP standards., • Develop and implement strategies to continuously improve GMP compliance., • Quality Systems Management:, • Maintain and improve the company's quality management system (QMS)., • Identify areas for process improvement and implement effective quality control measures., • Collaborate with cross-functional teams to ensure alignment with quality objectives., • Corrective and Preventive Actions (CAPAs):, • Lead investigations into quality issues and non-conformances., • Develop CAPA plans to address root causes and prevent recurrence of quality issues., • Monitor and track the implementation of CAPAs to ensure effectiveness., • Deviations Management:, • Investigate deviations from established procedures and specifications., • Document deviations and assess their impact on product quality., • Develop and implement corrective actions to address deviations and prevent recurrence., • Document Control:, • Establish and maintain document control procedures for quality documents., • Ensure the accuracy, completeness, and integrity of quality-related documentation., • Manage document change control processes and maintain document repositories., • Standard Operating Procedures (SOPs):, • Develop, review, and update SOPs to reflect current best practices and regulatory requirements., • Ensure SOPs are followed consistently throughout the organization., • Provide training and support to employees on SOPs and quality processes. Qualifications: • Bachelor's degree in a related field preferred (e.g., Quality Assurance, Chemistry, Biology, Engineering)., • Previous experience working in a manufacturing environment, preferably in a regulated industry (e.g., pharmaceuticals, medical devices, food)., • Strong understanding of Good Manufacturing Practices (GMP) and regulatory requirements (e.g., FDA, ISO)., • Experience with quality systems management, CAPAs, deviations, document control, and SOPs., • Excellent analytical and problem-solving skills., • Effective communication and collaboration abilities. Must be able to read, write, and speak in English. Bilingual preferred. Cosmetic Solutions LLC. is committed to equal employment opportunity for all employees and applicants for employment without regard to age, color, creed, disability status, gender, national origin, race, religion, sexual orientation or veteran status, or any other legally protected status.

Job Description * Who we are: Cosmetic Solutions is a leading manufacturer of cosmetic and OTC products, committed to innovation, quality, and continuous improvement. Our Quality Control team plays a vital role in ensuring our products meet the highest standards of safety, efficacy, and compliance. • We are seeking a detail-oriented and proactive Quality Control Technician to join our Raw Materials team. This role is essential to maintaining product integrity and regulatory compliance through rigorous testing and documentation practices., • Quality Control Lab Technician Major Responsibilities • Sample all incoming raw material for Quality control testing, • Conduct daily quality control testing, • Water, • Maintain the raw material standards library, • Conduct routine and non-routine testing of raw materials, in-process items, and finished goods., • Maintain retained sample inventory and storage area., • Calibrate and maintain lab equipment (pH meter, viscometer, balances)., • Review and follow SOPs, specifications, and related documentation., • Compile, interpret, and report analytical data., • Troubleshoot instruments and initiate investigations for anomalies and deviations., • Ensure compliance with GLP, GMP, and SOPs., • Document test results accurately in lab notebooks and databases., • Collaborate with cross-functional teams to resolve quality issues and implement corrective actions., • Participate in writing SOPs, OOS reports, deviations, CAPAs, and investigations., • Support sample testing, data entry, and coordination with external labs/vendors., • Promote and demonstrate company core values and participate in 6S lean initiatives., • Maintain a clean and organized lab environment., • Perform other duties as assigned by management., • Support the daily execution of the Quality Management System QUALIFICATIONS: • Written/oral communication skills required., • 2-3 years of experience in the Cosmetic or pharmaceutical industry preferred., • Experience in cosmetics, pharmaceuticals, or other FDA-regulated industries., • Strong knowledge of GLP, GMP, and regulatory standards., • Experience in a regulated laboratory environment., • Excellent attention to detail and organizational skills., • Strong problem-solving and analytical abilities., • Effective communication and teamwork skills., • Proficiency in Microsoft Office and laboratory data systems., • Ability to work independently and manage multiple priorities. Cosmetic Solutions LLC. is committed to equal employment opportunity for all employees and applicants for employment without regard to age, color, creed, disability status, gender, national origin, race, religion, sexual orientation or veteran status, or any other legally protected status.

Job DescriptionSalary: Job Summary: AirQuest is seeking a Certified Industrial Hygienist candidate to support our industrial hygiene services at military installations and government entities across the United States. The candidate will work out of our Fort Lauderdale, Florida location. Specific Responsibilities: • Perform a full range of occupational and environmental health engineering duties, including:, • Conduct industrial hygiene breathing zone and general area time weighted average (TWA) or short term exposure limit (STEL) air sampling., • Conduct ventilation surveys., • Conduct noise dosimetry., • Conduct indoor air quality (IAQ) evaluations., • Conduct ergonomic evaluations., • Conduct indoor firing range evaluations., • Perform industrial hygiene annual and periodic follow-ups to meet regulatory and/or client requirements, • Conduct health hazard evaluation of work areas while hazardous materials are being managed or during planned abatement activities, • Conduct detailed risk assessments, with special emphasis on occupational health-risk assessments of occupational exposures., • Input data as required into Defense Occupational and Environmental Health Readiness System (DOEHRS) MIS., • Perform and manage various tasks, including performing material surveys and maintaining databases (including DOEHRS) for industrial hygiene and environmental health surveillance., • Analyze the results of sampling and measurement, and recommending corrective action or mitigation to reduce health risk to the building occupants or workers performing tasks where hazardous materials are encountered., • Assess the use of respiratory protection, conduct fit-testing and training for tight-fitting and loose fitting respiratory protection., • Train industrial personnel on work place hazards., • Develops and implements industrial hygiene/environmental health and safety programs and procedures in assigned area of specialization such as respiratory protection, occupational noise, indoor air quality, asbestos, lead, and local exhaust ventilation., • A Bachelors degree in science or engineering that included courses in any combination of chemistry, physics, engineering, environmental science, biology, or industrial hygiene or a related field from an ABET-accredited institution., • 3 years of relevant work experience in the industrial hygiene, safety profession, or one of its specialties., • Must be able to read, understand, speak, and write English proficiently to effectively communicate with all clients, management, staff and administrative personnel., • Ability to analyze the data acquired, predict probable effects of exposures on the health and well-being of workers, and select and recommend appropriate controls, including management procedures, medical issues and evaluations, engineering controls, education or training needs, and personal protective equipment that may be required or recommended., • Must be able to use standard office equipment, such as computers, typewriters, copiers, fax machines, and telephone systems., • Must have excellent communications and customer service skills and use of occupational and environmental health and safety terminology., • Must be a Certified Industrial Hygienist, • Masters degree that is ABET-accredited in a job-relevant program of study (e.g., industrial hygiene, occupational health, or environmental health), • Five or more years of experience in or with the U.S. Air Force Bioenvironmental Engineering career field or a closely related Department of Defense (DOD) program or civilian equivalent is desired, • Familiarity with Bioenvironmental Engineer concepts, practices, and procedures., • Possess an active security clearance or able to obtain one, • Basic experience with DOEHRS., • Knowledge of OSHA, NIOSH, ANSI and ACGIH standards, • Knowledge of asbestos, lead/lead-based paint and fungal management programs, • Knowledge of ventilation systems, • Experience conducting exposure assessments, • Experience recognizing hazards, • Experience addressing environmental health and safety concerns, • Experience preparing technical reports, • Ability to perform environmental and industrial hygiene surveys, including sampling and monitoring, • Ability to operate various industrial hygiene monitoring equipment, • Ability to diplomatically explain and interpret environmental health and safety principles., • Ability to work with people of all ages and diverse constituencies., • Thorough knowledge of applicable environmental health and safety regulations, • Thorough knowledge and demonstration of industrial hygiene principles and practices, • Excellent computer skills including MS Office applications, • Effective communication skills, • Excellent writing skills, • Capable of managing multiple projects and the technicians that may be involved in projects, • Strong training and interpersonal skills, • Valid drivers license, • Ability to pass a background check, • Ability to pass a drug test, • Ability to work long hours when necessary, • Frequent out of town travel, • Must be able to wear personal protective equipment such as, hard hats, hearing protection, safety glasses, respirators, protective footwear and other safety devices such as fall protection harnesses and others as necessary, • Must be able to walk on uneven surfaces, carry and climb ladders and stand for extended periods of time, • Must be able to work in an outdoor environment All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.

Job Description Part-Time (Temporary/Seasonal) Lab Technician Location: Miami Plant Are you looking for an opportunity to join an established and stable industry leader that is rapidly growing and where employees are our number one asset? Do you want a role where your contributions support important environmental operations and compliance? If so, we are looking for you! Cliff Berry, Inc. has an exceptional part-time (temporary/seasonal) opportunity for a qualified Lab Technician at our Miami plant. The Lab Technician will support laboratory operations by preparing chemical solutions, conducting wet chemistry testing on incoming waste and finished products, and ensuring compliance with quality assurance and regulatory requirements. This position provides critical support to maintain plant quality standards while gaining valuable industry experience. Essential Functions Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. • Follow all health and safety policies and procedures, ensuring safety is the number one priority., • Collect, analyze, and record data on incoming and outgoing products, water, and waste streams., • Perform sampling and testing per ASTM standards., • Accurately maintain records, logs, and compliance documentation., • Enter analytical data into SAP and maintain trackers for incoming loads., • Assist in ordering and organizing laboratory supplies., • Calibrate, maintain, and perform basic preventive maintenance on lab equipment., • Interpret test results, ensuring compliance with all local, state, and federal regulations., • Safely handle and store chemicals, reagents, and solutions while maintaining inventory., • Support R&D testing and evaluation as directed by the Lab Manager., • Bachelor’s degree in Science with a concentration in Chemistry or Biology and 1 year of wet-lab experience; or, • Associate degree in Chemistry or Biology with at least 2 years of QA/QC laboratory experience., • Prior environmental industry experience., • Ability to work in a fast-paced environment and manage multiple tasks., • Strong attention to detail and accuracy., • Effective communication and teamwork skills., • Ability to lift 20 pounds consistently., • Ability to stand, sit, or walk for up to 4 hours at a time. This position requires working in a laboratory and plant environment with possible exposure to extreme temperatures, humidity, and both hazardous and non-hazardous chemicals. Compliance with all company, federal, state, and local safety regulations is mandatory. Cliff Berry, Inc. is an Equal Employment Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, national origin, ancestry, sex (including pregnancy), sexual orientation, gender identity, age, physical or mental disability, veteran status, genetic information, ethnicity, citizenship, or any other characteristic protected by law.

Job Description We are seeking a detail-oriented and proactive Formulator Assistant to join our Product Development team. This role is ideal for someone with a background in Chemistry, Biology, Food Science, or a related field, and at least one year of experience in a regulated industry such as nutraceuticals, pharmaceuticals, or food. Qualifications: • Bachelor’s degree in Chemistry, Biology, Food Science, or related field., • At least 1 year of experience in a laboratory, formulation, R&D, or regulatory role within an FDA-regulated industry (nutraceutical, pharmaceutical, food, medical devices, personal care, etc.)., • Ability to perform basic calculations (percentages, concentrations, unit conversions, pricing)., • Draft formulations for quotes, lab batches, pilots, and testing during product development., • Troubleshoot formulations based on lab, pilot, testing outcomes, and pricing adjustments., • Conduct basic physical and organoleptic testing (e.g., weighing, particle size measurement)., • Review regulatory documentation to ensure compliance in formulation., • Log and track new raw materials for assigned projects., • Maintain accurate formulation records and track development progress., • Write change controls and deviation documents related to formulations., • Communicate project updates to the R&D Manager regularly., • Participate in meetings with clients, suppliers, and cross-functional teams as needed.

Job Description We are currently seeking a detail-oriented and motivated Regulatory Affairs Specialist. This role is crucial in ensuring that our products comply with all regulatory requirements. If you are passionate about regulatory affairs and looking for an opportunity to grow within a dynamic company, we encourage you to apply. Responsibilities: • Prepare, review, and submit regulatory documents to ensure compliance with FDA and other regulatory authorities., • Maintain up-to-date knowledge of regulations, guidelines, and standards relevant to the pharmaceutical industry., • Assist in the preparation of regulatory submissions including New Drug Applications (NDAs), Investigational New Drug Applications (INDs), and amendments., • Coordinate with cross-functional teams to gather necessary information for regulatory submissions., • Ensure timely and accurate communication with regulatory authorities., • Monitor and track the progress of submissions and respond to any inquiries from regulatory bodies., • Assist in the development and implementation of regulatory strategies to support product approvals and lifecycle management., • Bachelor’s degree in a related field such as biology, chemistry, or pharmaceutical sciences., • Previous experience in a regulatory affairs role within the pharmaceutical industry is preferred., • Strong understanding of FDA regulations and guidelines., • Excellent organizational and time management skills., • Strong attention to detail and ability to handle multiple projects simultaneously., • Effective communication skills, both written and verbal., • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)., • Ability to work independently and as part of a team.

Advance your career with Mindlance! We have been connecting talented professionals with world-class companies since 1999. Mindlance is here to help you to find the perfect fit with just the right company. Currently, we are seeking a Medical Laboratory Scientist for an exciting career growth opportunity. Make your next big career move with the kind of position that will allow you to be genuinely passionate about the work you do! Our recruiters and team will work closely with you to help you get the edge over the competition. Let Mindlance advocate for you – apply today! Job Title: Medical Laboratory Scientist. Job Location: Shreveport LA 71104 Pay Rate Range: $35/hr. to $40/hr. on W2. Duration: 4+ months (As of now it is only a Temp assignment for 04 Plus months and will be hired full time perm too.) 40 hours a week. Mon - Fri 8am - 5pm Summary: This position is accountable for performing clinical laboratory testing, following all applicable policies and procedures. Duties and Responsibilities: OB RESPONSIBILITIES: 1. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result;, 2. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens;, 3. Analyze specimens using approved testing procedures (see department SOPs)., 4. Review and release test results., 5. Follow CLIA, HIPAA, OSHA, and safety guidelines as described in their respective guidelines., 6. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and all maintenance performed;, 7. Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance., 8. Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor., 9. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications., 10. Follow department's procedure in reporting STATS or Critical results to clients., 11. If applicable, answer questions from customers or other lab personnel., 12. Maintain complete records of all testing performed on-site., 13. Maintain general appearance of the department., 14. Make sure reagents/test kits have received dates, expiration dates, and if applicable opened dates. 15. Review/train on new procedures., 15. Attend monthly department and any additional training/educational meetings., 16. Participate in all applicable safety training sessions. Know the location and contents of the safety manual. Know the location/use of all applicable safety equipment., 17. If needed, participate in government or regulatory agency inspections., 18. Perform other duties as directed by supervisor. Required Knowledge: A solid understanding of basic laboratory testing is required for this position. The successful candidate must possess good computer skills and be able to adapt to working in multiple computer systems. Must have knowledge of QC and QA as well as knowledge of all areas of the laboratory. Required Work Experience: • 1 year Clinical experience (high complexity testing) required., • Minimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology., • National and State licensure as required. Education: BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990. Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). United States educated candidates must provide a detailed original transcript. EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

Job DescriptionActalent is Hiring a Team of Biomedical Technicians // First Shift!! Job Description The Senior Representative will be a highly proficient and quality-focused producer of Pre-Operative Plans. The role requires a focus on individual production efforts to meet team and department production targets. Responsibilities • Create cases to be completed using a proprietary case management system., • Review CT Scans for conformity to surgical protocol., • Segment CT Scans using specialized software to create 3D Anatomical Bone Models for use in Robotic Surgery., • Create Pre-Operative Surgical Plans using Digital Bone Models for robotically assisted Total Hip and Total Knee Replacement., • Review CT segmentations and Surgical Plans for accuracy of anatomical landmark selection, and implant sizing and positioning., • Upload completed Pre-plans to field-based personnel., • Document all activities according to prescribed methods and procedures., • Proficiency in biology, biological science, and biomedical science., • Data entry skills., • Proficiency in Microsoft Office Suite., • Experience with Salesforce or Materialize MIMICS., • Knowledge of Adobe Photoshop., • Proficiency in English (speaking and reading)., • Ability to view and distinguish between a variety of colors on a computer screen., • High School Diploma or equivalent., • Minimum of 2 years’ work experience or equivalent education (Associate's Degree or above)., • Certifications or related experience in Radiology (CT, X-Ray, MRI)., • Certification in Nursing or related field., • Completion of college-level anatomy courses., • Demonstrated customer service orientation., • Demonstrated interpersonal and communication skills. This is an onsite position with core hours from 7am-3:30pm, Monday through Friday. The demand continues to grow, leading to a high need for overtime, though infrequent, with potential weeks exceeding 55 hours. This is not a remote position. Pay and Benefits The pay range for this position is $20.00 - $20.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Oct 24, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Who we are: Cosmetic Solutions is a leader in the development and manufacturing of scientifically proven, innovative personal care products. With a focus on, face, body, hair, OTC, and professional use formulations, we create some of the most cost effective, high quality and powerful products on the market. Providing world class services to up and coming businesses, large established brands, physicians, estheticians and other skin care professionals; we specialize in research & development, custom formulization, graphic design, manufacturing, packaging and delivery. Senior Director Quality Assurance Job Overview Seeking an accomplished and integrity-driven quality professional offering over 20 years of Laboratory Management, Quality Systems Management (QSM), and Compliance experience in highly regulated sectors. The Senior Director of Quality will create and maintain a quality culture throughout the entire corporation. In addition, this position will develop and lead the business strategic quality plan in collaboration with the Executive Leadership Team (ELT) and other business unit senior leaders. This role provides strategic decision-making, leadership, planning, and prioritization to meet business and quality/compliance objectives. The Senior Director of Quality Assurance will focus on influencing how the functional vision and implementation plans align with the core strategic vision and business objectives. Responsibilities • Analyzes data to identify process improvement opportunities, • Documents improvement action plans for processes and projects assigning the responsibilities to the various teams, • Carries out project review meetings to ascertain progress, • Works on Client Quality requirements to identify adequate process controls, • Establishes Quality Assurance Plan for new projects, • Studies processes, documents the flow and identifies opportunities to automate, or eliminate steps leading to improved turn-around-time., • Designs dashboards for reporting, • Coordinates with various internal teams to drive actions, • Carries out Root Cause Analysis of errors to prepare action plans, • Trains, mentors and guides other members in the team on various Quality concepts, • Maintains quality assurance staff job results by coaching, counseling, and disciplining employees; planning, monitoring, and appraising job results., • Implements and acts in accordance with the organization’s information security HR and corporate policies., • Maintains quality assurance staff by recruiting, selecting, orienting, and training employees., • Protects assets from unauthorized access, disclosure, modification, destruction or interference., • Oversees the production process, ensuring compliance with industry standards, and managing quality assurance processes., • Develops and implements a comprehensive quality control plan, including procedures, processes, and guidelines to ensure that products meet quality specifications and adhere to regulatory requirements., • Heads process monitoring and improvement: Monitor production processes to identify any deviations from the established quality standards, investigate root causes, and initiate corrective actions. Continuously seek ways to improve processes to enhance product quality and reduce waste., • Quality assurance: Develop, implement, and maintain a robust quality assurance system that ensures products are consistently manufactured according to predefined specifications and in compliance with applicable regulations and standards (e.g., GMP, ISO, and FDA)., • Documentation: Create, maintain, and update all necessary quality control and quality assurance documentation, including standard operating procedures (SOPs), batch records, quality control reports, and certificates of analysis (COTraining and development., • Ensure that all personnel involved in the production process receive appropriate training in quality control procedures, equipment operation, and safety protocols. Regularly review and update training materials to keep them current and relevant., • Equipment calibration and maintenance: Ensure that all equipment used in production is properly calibrated and maintained to guarantee accurate and reliable results. Schedule and oversee regular equipment maintenance and calibration activities., • Inspection and auditing: Conduct regular internal audits and inspections to ensure adherence to quality control procedures and regulatory requirements. Prepare for and participate in external audits by regulatory agencies and clients., • Supplier management: Evaluate, select, and monitor suppliers to ensure that raw materials and components meet quality specifications and comply with industry standards. Work closely with suppliers to address any quality issues that may arise., • Investigate and address customer complaints related to product quality, initiating corrective actions as necessary to prevent similar issues from occurring in the future., • Reporting: Generate regular quality control reports to track key performance indicators (KPIs) and present findings to senior management. Communicate with cross-functional teams to ensure that quality objectives are understood and achieved., • Leading, managing, and supervising a team of quality control inspectors. This involves: Recruitment and selection: Hire and onboard new quality control inspectors as needed, ensuring they possess the necessary skills, knowledge, and experience to effectively perform their duties., • Training and development: Provide ongoing training, guidance, and support to the quality control inspectors to help them understand their roles and responsibilities, as well as keep them up to date with industry standards and best practices., • Performance management: Set performance goals and objectives for the quality control inspectors, monitor their progress, provide regular feedback, and conduct performance evaluations. Address any performance-related issues promptly and effectively., • Delegation and task assignment: Assign specific tasks and responsibilities to the quality control inspectors based on their expertise, ensuring that all aspects of the quality control process are adequately covered., • Communication and collaboration: Foster an open and transparent work environment that encourages communication and collaboration among the quality control team members. Hold regular team meetings to discuss ongoing projects, address concerns, and share updates., • Motivation and engagement: Create a positive work atmosphere by recognizing and rewarding outstanding performance, addressing team concerns, and providing opportunities for professional growth and development. Requirements Skills, Abilities, And Experience • Demonstrated success in creating and maintaining a culture of quality in a contract manufacturing organization, • Broad system, production, and supply chain experience that shows a proven track record of leading and managing quality & reliability requirements, • Knowledgeable and experienced in performing internal and external quality audits., • Site liaison, coordinator, and lead for all current and future regulatory agencies., • Knowledgeable and experienced in planning, coordinating, and leading QMS management reviews., • Knowledgeable and experienced in producing Annual Product Reviews for OTC formulas., • Root cause / corrective action expertise, • Create and communicate an overall vision for quality within the company, setting goals and recommending organizational changes to achieve these goals., • Communicate the company’s quality system to customers., • Create an environment conducive to continuous quality improvement and implement systems to nurture quality excellence., • Direct activities of company-wide quality staff and departmental activities to ensure product quality through test procedures and processes., • Lead and facilitate workshops that provide immediate improvement results., • Provide leadership and guidance to the quality and contract manufacturing teams, fostering a culture of excellence, collaboration and continuous improvement. Preferred Qualifications: • Minimum of 10 years of experience in quality assurance and quality control, • Minimum bachelor’s degree in chemistry, biology, microbiology or similar life sciences or technical field such as engineering, mathematics, etc., • Detail-oriented, analytical, and able to manage multiple tasks in a fast-paced environment., • Extensive knowledge of FDA regulated industries, • Strong facilitation, influencing, organizing, and presentation/communication skills., • Well-developed written and verbal communication skills., • Hands-on experience with all levels of manufacturing, formulation and quality assurance., • Excellent at regulations interpretation and implementation., • Skill sets include strong analytical and problem-solving abilities with a propensity for instituting rapid change in difficult situations., • Positive, team-focused approach and proven leadership track record, including people development and project management., • A demonstrated track record of process and productivity improvement and successful results with developing and implementing change initiatives., • Experience and understanding of FDA Regulations & Audits, Title 21 of CFR 700, 820, 211, ISO Standards, Organic Certification, GMP, ISO 17025:2017, • General Requirements for the Competence of Testing and Calibration Laboratories, • FL Department of Health & FL Department of Agriculture and Consumer Services, • Strong tenure in previous positions., • Experience on both sides of the audit table. Experienced third party / client auditor.

Job Description American Heritage Schools of Broward County is currently accepting applications for the following specialities: • Upper Level Sciences (Marine Bio., Biology, Chemistry, Physics, Computer Science), • English (Jr. high & high school),, • Math (Jr. high & high school), • Reading Specialist, • History, • Elementary Education, • Looking for LIVE tutors (not online initially, • B.A./B.S. from an accredited institution is required

Job DescriptionSalary: Job Summary AirQuest is seeking a Bioenvironmental Engineer/Certified Industrial Hygienist candidate to support our industrial hygiene services at military installations and government entities across the United States. The candidate will work out of our Fort Lauderdale, Florida location. Specific Responsibilities • Perform a full range of occupational and environmental health engineering duties, including:, • Conduct industrial hygiene breathing zone and general area time weighted average (TWA) or short term exposure limit (STEL) air sampling., • Conduct ventilation surveys., • Conduct noise dosimetry., • Conduct indoor air quality (IAQ) evaluations., • Conduct ergonomic evaluations., • Conduct indoor firing range evaluations., • Perform industrial hygiene annual and periodic follow-ups to meet regulatory and/or client requirements, • Conduct health hazard evaluation of work areas while hazardous materials are being managed or during planned abatement activities, • Conduct detailed risk assessments, with special emphasis on occupational health-risk assessments of occupational exposures., • Input data as required into Defense Occupational and Environmental Health Readiness System (DOEHRS) MIS., • Perform and manage various tasks, including performing material surveys and maintaining databases (including DOEHRS) for industrial hygiene and environmental health surveillance., • Analyze the results of sampling and measurement, and recommending corrective action or mitigation to reduce health risk to the building occupants or workers performing tasks where hazardous materials are encountered., • Assess the use of respiratory protection, conduct fit-testing and training for tight-fitting and loose fitting respiratory protection., • Train industrial personnel on work place hazards., • Develops and implements industrial hygiene/environmental health and safety programs and procedures in assigned area of specialization such as respiratory protection, occupational noise, indoor air quality, asbestos, lead, and local exhaust ventilation., • Performs other duties as assigned. Required Skills & Qualifications: • A Bachelors degree in science or engineering that included courses in any combination of chemistry, physics, engineering, environmental science, biology, or industrial hygiene or a related field from an ABET-accredited institution., • 3 years of relevant work experience in the industrial hygiene, safety profession, or one of its specialties., • Must be able to read, understand, speak, and write English proficiently to effectively communicate with all clients, management, staff and administrative personnel., • Ability to analyze the data acquired, predict probable effects of exposures on the health and well-being of workers, and select and recommend appropriate controls, including management procedures, medical issues and evaluations, engineering controls, education or training needs, and personal protective equipment that may be required or recommended., • Must be able to use standard office equipment, such as computers, typewriters, copiers, fax machines, and telephone systems., • Must have excellent communications and customer service skills and use of occupational and environmental health and safety terminology., • Willingness to travel to client locations domestically and internationally, on an as-needed basis. Preferred Skills & Qualifications: • Certified Industrial Hygienist accreditation is desired (the ability to obtain the accreditation is required)., • Degree that is ABET-accredited in a job-relevant program of study (e.g., industrial hygiene, occupational health, or environmental health), • Five or more years of experience in or with the U.S. Air Force Bioenvironmental Engineering career field or a closely related Department of Defense (DOD) program or civilian equivalent is desired, • Familiarity with Bioenvironmental Engineer concepts, practices, and procedures., • Possess an active security clearance or able to obtain one, • Basic experience with DOEHRS., • Successful, demonstrated project and program management experience Minimum Competencies: (Skills, knowledge, and abilities.) • Knowledge of OSHA, NIOSH, ANSI and ACGIH standards, • Knowledge of asbestos, lead/lead-based paint and fungal management programs, • Knowledge of ventilation systems, • Experience conducting exposure assessments, • Experience recognizing hazards, • Experience addressing environmental health and safety concerns, • Experience preparing technical reports, • Ability to perform environmental and industrial hygiene surveys, including sampling and monitoring, • Ability to operate various industrial hygiene monitoring equipment, • Ability to diplomatically explain and interpret environmental health and safety principles., • Ability to work with people of all ages and diverse constituencies., • Thorough knowledge of applicable environmental health and safety regulations, • Thorough knowledge and demonstration of industrial hygiene principles and practices, • Excellent computer skills including MS Office applications, • Effective communication skills, • Excellent writing skills, • Capable of managing multiple projects and the technicians that may be involved in projects, • Strong training and interpersonal skills, • Exhibits positivity, integrity and responsibility Requirements: • Valid drivers license, • Ability to pass a background check, • Ability to pass a drug test, • Ability to work long hours when necessary, • Frequent out of town travel (up to 40% of the time), • Must be able to wear personal protective equipment such as, hard hats, hearing protection, safety glasses, respirators, protective footwear and other safety devices such as fall protection harnesses and others as necessary, • Must be able to walk on uneven surfaces, carry and climb ladders and stand for extended periods of time, • Must be able to work in an outdoor environment All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.

Job DescriptionGoldson Spine Rehabilitation Center (GSRC) is a multi-disciplinary practice that has been in business for over 25 years. Our services include chiropractic, physical therapy, massage therapy, and psychotherapy with five locations across the southeastern region of Florida. We operate under the mission “To provide the most courteous and effective care and increase the well-being of every person who walks through our door”. The company is seeking a part-time Medical Scribe to assist our physicians with increasing their efficiency and productivity by managing patient information, medical histories, physician exams, treatments, and services provided. Purpose: To assist the physician as a scribe to increase the physician’s efficiency and productivity by managing patient information, medical histories, physician exams, test results, treatments, and services provided. Schedule: M-W-F 8 am-6 pm Responsibilities: • Be proficient in documenting patient information in Chiro Touch., • Consult with chiropractors and physical therapists to make sure the information is accurate., • Attend monthly and quarterly office meetings in addition to annual events., • Ensure medical reports for patients (i.e. initial, re-exam, and final) are completed and submitted to be reviewed and signed by the Chiropractors and Physical Therapists who completed that evaluation., • Responsible for obtaining all missing contents needed to complete medical reports., • Ensure patient paperwork and reports are completed in a timely manner., • Ensure that all medical request forms from attorneys are scanned in the patient’s file in Chirotouch., • Responsible for posting Diagnoses in Chirotouch if not done by the Chiropractors and Physical Therapists., • Responsible for releasing medical records and information to authorized persons (i.e. lawyers, insurance companies, and patients. via (fax, email, or mail)., • Providing medical information by answering questions and requests of patients, lawyers, insurance companies etc., • Assist with organizing and maintaining health information both in paper files and in electronic systems., • Abides by HIPAA laws regarding sharing of personal medical information., • Attends to email correspondence. Skills & Abilities: • Good written and verbal communication skills in English, and able to communicate to a diverse range of people clearly and effectively, • Good use of a computer, printer, fax, scanner, and copier machines, • Ability to work in and contribute to the team, • Ability to provide excellent customer service, • Ability to multitask while still paying attention to the details, • Good time management skills Minimum Qualifications (either degree area is preferred): Bachelor of Science in Health Education Bachelor of Science in Exercise and Sports Science Bachelor of Science in Biology Compensation: $15 - $17

Job Description Are you a Marine Biology or Environmental Sciences student eager to gain hands-on experience in the aquarium industry? Nature Aquariums, located in the heart of Broward County, Florida, is offering a 12 to 16-week unpaid internship designed to provide comprehensive exposure to both marine and freshwater aquatic life. About Us: At Nature Aquariums, we are passionate about the well-being and care of aquatic life. Our holistic approach emphasizes educating customers to ensure the best possible care for their aquatic pets. As a growing store, we offer a dynamic environment for learning and professional development. Internship Responsibilities: • Greet and assist customers in our showroom., • Support the team with aquarium and system maintenance., • Engage in hands-on projects to learn various aspects of the aquarium trade., • Develop proficiency in identifying and caring for marine and freshwater flora and fauna. What We Offer: • Close-up experience with a diverse range of marine and freshwater species, including fish, invertebrates, corals, and plants., • Real-world experience in diagnosing and correcting water chemistry and aquatic health issues., • Exposure to a retail environment, enhancing professional customer interaction skills., • Basic business experience in a for-profit setting., • Ongoing coaching and feedback throughout the internship., • Assistance in obtaining academic credit, if applicable., • A letter of recommendation upon successful completion of the program. Schedule: • Duration: 12 to 16 weeks., • Commitment: 15-25 hours per week, including Saturdays and/or Sundays, with flexibility to accommodate academic schedules. Qualifications: • Customer service experience preferred but not required., • Prior knowledge of aquarium fish keeping is advantageous but not essential., • Proficiency in additional languages, particularly Spanish, is a plus., • Ability to work effectively in a team-based environment., • Positive attitude, discipline, and a drive to succeed., • Competence in using computer and smartphone software., • A passion for animals and comfort with hands-on tasks involving water. Application Process: If you are interested in this opportunity, please contact us to receive an application and initiate the interview process. We are happy to answer any questions you may have about the program. Contact Information: • Address: 5344 N. University Drive, Lauderhill, FL 33351, • Phone: 754-223-3104 Join us at Nature Aquariums for an enriching internship experience that will enhance your knowledge and skills in the aquatic industry.

Job Description Funky Buddha Brewery, located in Oakland Park, Florida, is seeking a full-time Brewer to join its growing team. Established in 2010 at its Boca Raton brewpub, Funky Buddha is known for pushing the boundaries of traditional brewing methods with culinary-inspired recipes utilizing all-natural, food-centric ingredients. Some of its best-known beers include flagships Hop Gun IPA and Floridian Hefeweizen. This fast-growing company is the first production brewery in the greater Fort Lauderdale area and the largest brewery in South Florida and is positioned for rapid expansion over the next few years. “Where the Best Beers Are – Top 20 Brewpubs/Breweries for good beer” – USA Today“25 Breweries to Know” – Draft Magazine“10 Best Breweries to Visit in the South” – First We Feast JOB DESCRIPTION A shift brewer is responsible for all aspects of the brewing process including brewing, fermentation, cellaring, and finishing. This employee must be a hard-working, responsible, and self-motivated individual with a passion for craft beer and a desire to continue learning and growing within the industry. The candidate should also be a sociable person who is comfortable occasionally representing the brewery in public. Natural leadership, integrity, loyalty, and a good sense of humor are all factors in who we hire. Brewer tasks involve physical, mechanical, innovative, and problem-solving work so these skills are highly preferred. EXAMPLE OF DUTIES: ESSENTIAL FUNCTIONS • Operating brewhouse and producing batches from start to finish, • Following recipes and brewing process to achieve desired and consistent targets throughout batches, • Yeast handling and management, • Cellaring duties including fermentation management, • CIP (clean-in-place) of brewing and fermentation tanks, and other equipment, • Logging of all brewing related notes from brew day through fermentation, finishing, and packaging, • Following SOP (standard operating procedure) in each phase of brewing, fermentation, and packaging, • Maintaining clean brewing practices in the brewhouse and cellar, • Executing preventative maintenance on all brewhouse and cellar equipment, • Monitoring raw material inventory, • Updates job knowledge by participating in staff training opportunities In addition to performance of the essential functions, this position may be required to perform a combination of the following supportive functions, with the percentage of time performing each function to be solely determined by the supervisor based upon the particular requirements of the company. • Assist Brewery Manager with any necessary production duties., • Assist in any other special duties associated with beer production., • Assist with recipe development R&D, • Assist with Quality tasks, such as sensory evaluation of beer Near Vision Constant Far Vision Constant Hearing Constant Talking Constant Sitting Frequent Walking Frequent Computer Use Frequent Crouching, Bending, Stooping Frequent Reaching Occasional Grasping Occasional Pushing/Pulling Occasional Lifting/Carrying up to 55 lbs Occasional Climbing Stairs Occasional SAFETY REQUIREMENTS OSHA laws require the use of the following Personal Protective Equipment (PPE) when performing work duties that have the potential of risk to your health or safety: • Safety goggles when walking through the Production area, • Steel Toe rubber boots, • Safety gloves when handling industrial strength chemicals ORGANIZATIONAL RELATIONSHIPS No positions directly report to this position. SPECIFIC JOB KNOWLEDGE, SKILL AND ABILITY The individual must possess the following knowledge, skills and abilities and be able to demonstrate that he or she can perform the essential functions of the job, with or without reasonable accommodation, using some other combination of skills and abilities. • A strong passion for brewing modern American beers as well as the desire to push the boundaries of experimental brewing, • An advanced understanding of brewing aspects, including cellaring, yeast handling, CIP, and sanitization, • Strong organizational habits, a self-motivated work ethic, and good critical thinking/problem solving skills, • Flexibility in terms of hours and a willingness to work night shifts, weekends, and overtime, • Computer literate with some understanding of Microsoft Office/spreadsheet programs, • Ability to work safely with hazardous chemicals, • Ability to work safely in a wet, noisy, and non-temperature-controlled environment, • Ability to work safely in confined spaces and around complex machinery, • Ability to stoop, squat, kneel, and crawl for purposes of collecting samples, gathering data, and cleaning, • Ability to work independently on multiple projects at one time, maintaining attention to detail with each project, • Ability to meet production, quality and safety standards, • An understanding of operational structure and system variables such as pressure, temperature and flow is preferred, • Ability to problem-solve or understand mechanical failures related to brewing system EDUCATION Four-year college degree in natural sciences (e.g., microbiology, biochemistry, food science, engineering, etc.) preferred. EXPERIENCE Minimum of three years-experience in a commercial production industry, brewery or high-volume brew pub required. An understanding of quality assurance (QA) methods and techniques, laboratory operations, and basic knowledge of chemistry and biology preferred. Prior packaging, bottling, and racking experience preferred. Mechanical experience and aptitude preferred. Forklift operation or certification preferred. LICENSES OR CERTIFICATES No special licenses or certificates required. Funky Buddha Brewery is an Equal Opportunity Employer.

Job Description Funky Buddha Brewery, located in Oakland Park, Florida, is seeking a full-time Cellar Operator to join its growing team. Established in 2010 at its Boca Raton brewpub, Funky Buddha is known for pushing the boundaries of traditional brewing methods with culinary-inspired recipes utilizing all-natural, food-centric ingredients. Some of its best-known beers include flagships Hop Gun IPA and Floridian Hefeweizen. This fast-growing company is the first production brewery in the greater Fort Lauderdale area and the largest brewery in South Florida and is positioned for rapid expansion over the next few years. “Where the Best Beers Are – Top 20 Brewpubs/Breweries for good beer” – USA Today “25 Breweries to Know” – Draft Magazine “10 Best Breweries to Visit in the South” – First We Feast JOB DESCRIPTION The cellar operator is responsible for all aspects of processes related to fermentation, conditioning, treatment, clarification, carbonation, and any other processes required to achieve a final consistent product ready for packaging. The cellar operator must be a hard- working, responsible, and self-motivated individual with a passion for craft beer and a desire to continue learning and growing within the industry. The cellar operator should also be a sociable person who is comfortable occasionally representing the brewery in public. Cellar operator tasks involve physical, mechanical and problem-solving work so these skills are highly preferred. Also, Cellar department is responsible from most beer middle and end stage related tasks, so operator must be able to multitask through different processes in a fast-passed and fast-changing environment. EXAMPLE OF DUTIES: ESSENTIAL FUNCTIONS • Assistance with yeast handling and management, • Cellaring duties including fermentation management, • CIP (clean-in-place) of brewing and fermentation tanks, and other equipment, • Operation of centrifuge and plate filter for beer clarification, • Careful execution of treatment plans for specialty beers, • Maintain proper record keeping practices by logging product related notes from brew day through fermentation, finishing, and packaging, • Following SOP (standard operating procedure) in each phase of fermentation, clarification, carbonation and packaging, • Operation of flash pasteurizer, • Maintaining sanitary practices in all aspects of beer processing, • Executing preventative maintenance on all brewhouse and cellar equipment, • Preparation, filling, transfer of beer from liquor and wine barrels, • Assistance with lab testing and other Quality Assurance activities, • Updates job knowledge by participating in staff training opportunities, • This list is not exhaustive and job functions are subject to change to accommodate changing business needs SUPPORTIVE FUNCTIONS In addition to performance of the essential functions, this position may be required to perform a combination of the following supportive functions, with the percentage of time performing each function to be solely determined by the supervisor based upon the particular requirements of the company. • Assist Brewery Operations Manager with any necessary production duties., • Assist in any other special duties associated with beer production., • Assist any other special duties associated with quality checks., • May be asked to assist with other duties and special projects throughout the Brewery PHYSICAL REQUIREMENTS Near Vision Constant Far Vision Constant Hearing Constant Talking Constant Sitting Frequent Walking Frequent Computer Use Frequent Crouching, Bending, Stooping Frequent Reaching Occasional Grasping Occasional Pushing/Pulling Occasional Lifting/Carrying up to 55 lbs Occasional Climbing Stairs Occasional SAFETY REQUIREMENTS OSHA laws require the use of the following Personal Protective Equipment (PPE) when performing work duties that have the potential of risk to your health or safety: • Safety goggles when walking through the Production area, • Steel Toe rubber boots, • Hearing Protection in loud environments, • Safety gloves when handling industrial strength chemicals Employees will be trained in the proper use and care of assigned PPE. Funky Buddha Brewery provides the required PPE. It is your responsibility to report defective, damaged or lost PPE, or equipment that does not fit properly to your Manager. ORGANIZATIONAL RELATIONSHIPS No positions directly report to this position. SPECIFIC JOB KNOWLEDGE, SKILL AND ABILITY The individual must possess the following knowledge, skills and abilities and be able to demonstrate that he or she can perform the essential functions of the job, with or without reasonable accommodation, using some other combination of skills and abilities. • A strong passion for brewing and a desire to advance personal growth in the brewing industry, • Some understanding of brewing aspects, including cellaring, yeast handling, CIP, and sanitization, • Strong organizational habits, a self-motivated work ethic, and good critical thinking/problem solving skills, • Flexibility in terms of hours and a willingness to work night shifts, weekends, and overtime, • Computer literate with some understanding of Microsoft Office/spreadsheet programs, • Ability to work safely with hazardous chemicals, • Ability to work safely in a wet, noisy, and non-temperature-controlled environment, • Ability to work safely in confined spaces and around complex machinery, • Ability to stoop, squat, kneel, and crawl for purposes of collecting samples, gathering data, and cleaning, • Ability to work independently on multiple projects at one time, maintaining attention to detail with each project, • Ability to meet production, quality and safety standards, • An understanding of operational structure and system variables such as pressure, temperature and flow is preferred, • Ability to problem-solve or understand mechanical failures related to brewing system is preferred, • Open mind for cross-training and covering other department’s tasks related to beer production and quality QUALIFICATION STANDARDS EDUCATION Four-year college degree in natural sciences (e.g., microbiology, biochemistry, food science, engineering, etc.) preferred. EXPERIENCE Minimum of one-year experience in a commercial production on operations, brewery or high-volume brew pub required. An understanding of quality assurance (QA) methods and techniques, laboratory operations, and basic knowledge of chemistry and biology preferred. Prior packaging, bottling, and racking experience preferred. Mechanical experience and aptitude preferred. Forklift operation or certification preferred. LICENSES OR CERTIFICATES No special licenses or certificates required. GROOMING All employees must maintain a neat, clean and well-groomed appearance. Integrity, loyalty and a good sense of humor are all factors in who we hire. We are a rapidly expanding company with growth potential within. Funky Buddha Brewery is an Equal Opportunity Employer. If you think you have what it takes to join this exciting and growing company, please apply here. Calls, letters, faxes, carrier pigeon, or personal visits will not be accepted. By applying to this job, I certify that all information represented by me in this employment application is true, correct and complete to the best of my knowledge. I agree and understand that any falsification, omission or misrepresentation of information is grounds for withdrawal of an offer of employment and may result in my dismissal if discovered at a later date and I agree that Funky Buddha Brewery shall not be liable, in any respect, if any resulting employment is terminated because of misstatements or omissions made by me in this application.

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Job Description Enjoy what you do while contributing to a company that makes a difference in people’s lives. Florida Reproductive Specialists by IVF Florida is backed by one of the premier fertility centers in the United States. We continually seek experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward. We have an immediate opening for a full-time Laboratory Administrative Assistant - Embryology to join our team in Margate, FL. The schedule is working Tuesday-Saturday 7:00am-4:00pm. How You'll Contribute: We always do whatever it takes, even if it isn't specifically our "job." In general, the Laboratory Administrative Assistant - Embryology is responsible for: • Shipping, receiving and disposition of samples, • Ordering and receiving of lab supplies, • Performing administrative duties as necessary, • Assists laboratory personnel in performing lab services in accordance with Federal, State, and local laws and guidelines to ensure laboratory maintains proper accreditation, • Maintains a customer service oriented environment, • Makes suggestions on how to reduce lab supplies cost, • Maintains supply inventory by checking stock to determine inventory level, • Identifies improvement opportunities and participates in resolving problems that are identified, • Attends meetings, • Communicates in an open, assertive manner at all times, • Bachelors degree in Biology required, • Strong attention to detail, • Ability to communicate accurately and concisely, • Excellent oral and written communication, • Demonstrate motivation and flexibility What We Offer: We are proud to provide a comprehensive and competitive benefits package tailored to support the needs of our team members across all employment types: To learn more about our company and culture, visit here. How To Get Started: To have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen.

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