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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.

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 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 About Massive Bio Every cancer patient deserves access to treatment options. Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access clinical trials by eliminating the barriers of geography, financial constraints, and information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact globally by powering operations across multiple countries and bringing innovative cancer treatment options to a rapidly growing and diverse population of patients. Through our proprietary AI platform, we connect individuals to clinical trials worldwide and partner with leading pharmaceutical companies, contract research organizations (CROs), and healthcare systems to accelerate drug development and expand equitable access to cutting-edge therapies. We're recognized as a leader in health-tech innovation. Massive Bio was featured as #4 in Fast Company's Startup 100 list for Turkey and has raised $24M total funding from impact-driven investors including Revo Capital, the International Finance Corporation, and Cavendish Impact Foundation, validating both our business model and our mission-driven approach. About the Role As the primary owner of sponsor and biopharma client relationships, you’ll play a key part in shaping customer experience and driving delivery. You’ll lead client meetings, translate asks into actionable plans, and work cross-functionally to ensure commitments are met on time and with quality. This is a highly visible, client-facing position that demands strong presence, responsiveness, and sound judgment. You’ll embody best-in-class Customer Success and Account Management—where executive presence, fluent English, real-time handling of challenging questions, and thorough follow-up set the standard. Key Responsibilities * Manage a portfolio of sponsor and client accounts, leading recurring calls, business reviews, and ad-hoc engagements. Keep agendas, notes, and action items clear and up to date. * Drive responsiveness and service levels for sponsor requests, communicating with accuracy and awareness of business risks. Escalate, defer, or act decisively to ensure satisfaction. * Translate customer objectives into internal workstreams, collaborating across functions like Marketing, Provider Engagement, and Clinical Operations. Ensure deliverables are tracked to completion. * Maintain reliable data in CRM and operational systems, reporting on account status and key metrics. Prepare customer-facing reports and dashboards for regular reviews. * Develop presentations, progress decks, and documentation to support sponsors and partners. Ensure all materials are audit-ready and professionally presented. * Partner with Clinical Operations to collect and surface quality signals impacting client satisfaction. Identify and advocate for improvements that enhance sponsor experience. * Support account renewals and expansion by demonstrating value delivered, meeting key milestones, and highlighting business impact. Qualifications & Requirements * Bachelor’s degree required; life sciences (Medicine, Nursing, Biology, Pharmacology, Engineering) preferred. Business or analytics backgrounds welcome with relevant healthcare knowledge. * 3–7 years’ experience in Customer Success, Account Management, Clinical Operations, Sponsor Relations, or similar roles in health-tech, CRO, pharma/biotech, or healthcare services. * Demonstrated ability in leading client meetings, crafting precise follow-ups, and driving multi-disciplinary collaboration. * Executive presence and outstanding communication, including fluent English and real-time Q&A skills. * High sense of ownership, responsiveness, organization, and attention to detail. * Familiarity with the oncology trial process and privacy regulations like HIPAA/GDPR is a plus. * Comfortable using CRM and productivity tools; strong reporting skills in Excel/Slides. * No travel restrictions; able to travel occasionally for client engagements or industry events. Powered by JazzHR hsXNg296nS

Job Description Job Title: Medical Technologist Job Description Join our dynamic laboratory team as a Medical Technologist, where you will play a crucial role in patient care by preparing and testing patient samples. Your expertise will ensure the accuracy and reliability of laboratory results using advanced techniques and equipment. Responsibilities • Prepare patient samples for testing and determine the acceptability of specimens and results., • Repeat specimen testing as necessary to ensure accuracy., • Perform Hematology, Chemistry, and Urinalysis testing., • Conduct laboratory tests and procedures using techniques such as ELISA, RNA extraction, and flow cytometry., • Execute a variety of manual, semi-automated, and automated Biochemical, Hematological, Microbiological, and/or Blood Bank analyses on varied patient specimens., • Maintain, calibrate, operate, and troubleshoot laboratory instrumentation to ensure proper functionality., • Accurately prepare, label, and store reagents, standards, controls, and specimens for analysis., • Report accurate and timely test results to deliver quality patient care., • Participate in quality assurance and quality improvement activities., • Identify and replenish testing bench supplies as necessary., • Recognize normal, abnormal, unusual, and critical results and take appropriate action as established by laboratory policy., • Bachelor’s degree in Biology, Chemistry, Medical Technology, or other related science., • Certified Medical Technologist (MT), Medical Lab Scientist (MLS), or Clinical Laboratory Scientist (CLS). Certification must be from ASCP, NCA, AMT, or AAB., • Blood bank experience is required., • Experience working in a hospital or clinical laboratory., • Ability to interpret test results and apply them to patient care., • Proficiency in one of the following areas: hematology, clinical chemistry, coagulation, urinalysis, or microscopy. This is a Contract to Hire position based out of Deerfield Beach, FL. Pay and Benefits The pay range for this position is $38.00 - $38.00/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 Deerfield Beach,FL. Application Deadline This position is anticipated to close on Nov 21, 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 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 * 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 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 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.

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 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 Position & Client Overview: Our client -- one of the largest laboratory companies in the country -- currently seeks a histology technician to work in their busy anatomic pathology reference laboratory in the beautiful Fort Lauderdale area. This will be either a day or evening shift position. Salary Range: $40,000-85,000 This south Florida location is a beach-lovers paradise with its 24-miles of sandy beaches, but there are plenty of ways to off the beach with cultural attractions, luxurious spas, sightseeing & more. Broward County is home to 1.8 million residents in 31 cities sprawling across 1,200 square miles of landscape. With so much to explore, don't waste time; apply today! Job Summary: Perform routine specimen preparation which involves cutting various tissue types and mounting them on glass slides for examination under the microscope by the pathologist. Nationally certified histotechnician experienced in receiving, processing, and preparing patient tissue specimens for microscopic examination and analysis by the pathologist. Able to perform complex histologic procedures, recognize deviations from expected results, and analyze and correct problems using scientific principles learned from NAACLS training and 1 year of experience. Skill Requirements: • Calibrate, operate, troubleshoot and maintain the equipment, • Dexterity and good hand-eye coordination are required to collect and prepare specimens, • Lab safety and infection prevention is of paramount importance Responsibilities include but not limited to: • Remove tissue from a preservative solution, remove water from the sample, and replace it with paraffin wax, • Embed sample in a larger block of wax to prepare it for slicing before mounting it on a microtome, • Slice or section the sample then stain with special dyes and mount on a slide for viewing with a microscope Education, Certification, & Experience: • Associate or Bachelor's Degree or 60 semester hours (90 quarter hours) from a regionally accredited college/university with a combination of 12 semester hours (18 quarter hours) of biology and chemistry, • HT/L(ASCP) certification, • Or on the job trained/non certified per the lab approval, • One (1) year of experience at minimum HealthCare Connections, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, religion, national origin, disability, pregnancy, protected veteran status, sexual orientation, gender identity, genetic information or other protected status pursuant to law. #IND

Job DescriptionJob Title: QC Lab Technician - Cosmetics Job Description We are seeking a detail-oriented and reliable QC Laboratory Technician to join our manufacturing team. This role is essential to ensuring the quality and compliance of raw materials, in-process batches, and finished products. The ideal candidate will have a strong foundation in laboratory practices and a proactive approach to maintaining testing standards and equipment calibration. Responsibilities • Conduct quality control testing of raw materials, in-process, bulk, and finished product samples., • Record and manage third-party lab results related to product testing., • Calibrate in-house laboratory instruments and facility-wide scales., • Support other operational tasks as needed outside of core responsibilities.Essential Skills, • Prior laboratory experience., • Ability to work independently with minimal supervision., • Strong mathematical aptitude and ability to perform complex calculations., • Excellent time management and organizational skills.Additional Skills & Qualifications, • Associate degree (2-year) in Biology or Chemistry., • Proficiency in English (speaking, reading, writing)., • Bilingual candidates are a plus, but not required., • Math proficiency will be assessed via a skills test.Work Environment Work hours are from 7:30 AM to 4:00 PM. The work involves handling laboratory equipment and maintaining a clean and organized environment. The position requires adherence to safety standards and protocols. Job Type & Location This is a Contract position based out of Deerfield Beach, FL. Pay and Benefits The pay range for this position is $20.00 - $24.00/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 Deerfield Beach,FL. Application Deadline This position is anticipated to close on Nov 18, 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 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

Job DescriptionBenefits/Perks • Flexible Scheduling, • Competitive Compensation As an arborist, you will be responsible for keeping trees for public spaces and ensuring any old trees are taken down before they can fall and hurt a person or damage appropriately and for consulting with clients on their landscaping needs, planting new trees, maintaining and pruning trees, and removing dead or unwanted trees. You may also be required to monitor and maintain soil conditions, treat diseased trees, and apply pesticides. You are hard-working, a team player, and dedicated to performing quality work in all that you do. Experience as a landscaper is preferred, and a positive attitude is necessary! Responsibilities: • Meeting with clients to discuss their landscaping needs., • Assessing soil and space requirements for new trees., • Planting new trees or woody plants., • Identifying and treating diseased trees., • Trimming tree branches and pruning trees., • Testing and maintaining soil conditions., • Applying specialized tree fertilizers., • Applying pesticides if necessary., • Removing dead or unwanted trees.Qualifications:, • Certified arborist required, • Past experience as a landscaper/groundskeeper preferred, • Bachelors degree in botany, biology, or horticulture., • Proven work experience as an arborist., • Advanced knowledge of tree biology and tree anatomy., • Knowledge of soil biology and fertilizer compositions., • Familiarity with climbing equipment., • Ability to operate handsaws and mechanical devices., • Ability to work in all weather conditions and at heights., • Physically fit and able to lift heavy objects., • Good communication skills.The ideal candidate will also have additional skills, such as:, • Project Management skills, • Bi-lingualStrong problem-solving and critical-thinking skills, • Strong attention to detail Veterans are highly encouraged to apply.

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.

Location: Pompano Beach FL 33069.Duration: 3+(possible extension or conversion into permanent).ASCP certification and FL state licenseure.Routine embedding and microtomy needed.Perform routine and non-routine activities involved in the preparation of slides for microscopic evaluation by pathologist(

Possibility of extension or conversion) opportunity and a great way to start working with a top-tier healthcare organization!.Position Name: Technical Lab - Histotechnologist I.Prepare and process tissue specimens for microscopic evaluation following lab protocols.Embed tissue in paraffin, perform m

Make your impact as a BCBA at BASS ABA Therapy.Up to $40K in sign-on and relocation bonuses!.At BASS ABA Therapy, we help children with autism thrive through personalized, evidence-based care, and we know that starts with empowering our clinicians.Board Certified Behavior Analysts (BCBAs).Relocation

The ideal candidate will possess a strong background in biology, preferably with a Masters degree AND significant experience in hands on laboratory techniques. American Heritage Schools - Palm Beach Campus is seeking a passionate and knowledgeable instructor to lead its high-level Biology Honors cou

Join a dynamic structural biology group at the Wertheim UF Scripps Institute, where we push the boundaries of molecular visualization and membrane biology. The laboratory has outstanding cell biology, molecular biology, protein expression, purification, biochemistry, cryogenic electron microscopy, a

NEW Cytotechnologist Opening - Southeast Florida.A well-established healthcare provider is seeking a.This role involves screening gynecologic and non-gynecologic cytological specimens, including fine needle aspirations, and ensuring accurate diagnostic results.Responsibilities also include specimen

NEW Cytotechnologist Opening - Southeast Florida.A well-established healthcare provider is seeking a.This role involves screening gynecologic and non-gynecologic cytological specimens, including fine needle aspirations, and ensuring accurate diagnostic results.Responsibilities also include specimen

MD/PhD) in biological sciences such as immunology, molecular biology, cell biology, or biochemistry, with a strong international publication record. Degrees earned from an education institution outside of the United States are required to be evaluated by a professional credentialing service provider

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MD/PhD) in biological sciences such as immunology, molecular biology, cell biology, or biochemistry, with a strong international publication record. The Solt lab at The Herbert Wertheim UF Scripps Institute of Biomedical Innovation and Technology, Department of Immunology and Microbiology, is seekin

Bachelor's degree in Cytotechnology or related field.

Join a dynamic structural biology group at the Wertheim UF Scripps Institute, where we push the boundaries of molecular visualization and membrane biology. The laboratory has outstanding cell biology, molecular biology, protein expression, purification, biochemistry, cryogenic electron microscopy, a

The Clinical Research Coordinator is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the vision and mission of the company.The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data for the

Preference will be given to candidates with strong skills in RNA biology techniques, molecular biology, and biochemical methods. Postdoctoral Associate in RNA Chemical Biology. The Disney group is a chemical biology laboratory focused on developing rational approaches to design highly selective ther

RELOCATE TO VIRGINIA OPPORTUNITY.Join our esteemed team of healthcare professionals committed to advancing healthcare through cutting-edge research, comprehensive training, and compassionate care.UVA Health is an integrated health system with a world-class academic medical center that includes a lev

They will be responsible for running a multidisciplinary research program focused on understanding how learning and memory are encoded at the molecular level in the brain, using a variety of molecular and cellular biology techniques, vertebrate animal models, and bioinformatics tools. Must possess a

College degree, ARRT cert, FL licnese, prior experience.

MD/PhD) in biological sciences such as molecular biology, cell biology, cancer biology, or biochemistry, with a strong international publication record. MD/PhD) in biological sciences such as molecular biology, cell biology, cancer biology, or biochemistry, with a strong international publication re

Join a leading healthcare organization in Hillsboro Beach, FL as a full-time Cytotechnologist working the day shift.Bring your expertise to a dynamic hospital lab with a supportive team and enjoy a competitive sign-on bonus of up to $20,000 for qualified candidates.On-site in Hillsboro Beach, FL.Ful

Degrees earned from an education institution outside of the United States are required to be evaluated by a professional credentialing service provider approved by.

Bachelor's degree within specific subject area related to the position. Education Benefits: Tuition fee waiver at PBSC, tuition reimbursement, degree recognition award, educational leave, and more.

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Zack Group is seeking a travel Cath Lab Technologist for a travel job in Cooper City, Florida.Job Description & Requirements.Cath Lab Tech Tech’s for positions in Cooper City, Florida.The ideal candidate will possess a current state or equivalent compact license.This is a 4x10 days, 08:00:00-18:00

Host Healthcare is seeking a travel Cath Lab Technologist for a travel job in Margate, Florida.Job Description & Requirements.Host Healthcare Job ID #a1fVJ000007QlymYAC.Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determine

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Optometry Faculty – Nova Southeastern University (NSU Florida).Inspire the Next Generation of Optometric Leaders.Join Nova Southeastern University's College of Optometry and be part of one of the few universities nationwide with both M.At NSU, we believe in advancing vision science through innovat

Additional Qualifications: Bachelor's degree in Science, 3 Years of cytotechnologist experience preferred, Proficiency in Gynecologic Cytology.

Genie Healthcare is seeking a travel Cath Lab Technologist for a travel job in Davie, Florida.Job Description & Requirements.Genie Healthcare is looking for a Cardiology to work in Cath Lab Tech for a 13 weeks travel assignment located in Davie, FL for the Shift (4x10 Days-Please verify shift detail

Hybrid – 2 Onsite Days/Week | Full-Time.Are you passionate about innovation in the health and wellness space? Do you thrive at the intersection of science, formulation, and market-ready product development?.This critical role involves developing new products, qualifying cutting-edge ingredients, a

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Metabolic Research Institute is looking for a Full Time Clinical Research Coordinator for busy Clinical Research Center in West Palm Beach, FL.Research Coordinator experience 5+ years.MUST have at least 5 years of experience as a research coordinator to be considered for this role.Must have exceptio

TRS Healthcare is seeking a travel Cath Lab Technologist for a travel job in Aventura, Florida.Job Description & Requirements.TRS Healthcare Job ID #1398936.Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined.Posted job