Trabajos biology degree en Fort Lauderdale, FloridaCrear alertas

Complexity of Work: Requires critical thinking skills, effective communications skills, decisive judgment and the ability to work with minimal supervision. Extensive knowledge of clinical trial operations, research methodologies, and regulatory compliance in clinical research. Must be able to work in a stressful environment and take appropriate action. Required Work Experience: Five (5) years of health care work experience and two (2) years' supervisory experience required. Clinical training as part of post-secondary education preferred. Proven experience in leading and managing clinical research programs and teams in an academic, healthcare, or industry setting. Other Information: Additional Education Info: Master's degree in research, biology, chemistry, physical sciences, social sciences, public health, health sciences, math, statistics or related field of study. Education Equivalency: Bachelor's with, at least, seven (7) years of related experience in research, biology, chemistry, physical sciences, social sciences, public health, health sciences, math, statistics or related field of study. Memorial Healthcare System is a community of caregivers dedicated to delivering quality patient- and family-centered care. This passion for caring extends to our teammates, who support one another and create heartfelt connections that last a lifetime. We are one family at the heart of exceptional care. Join us as we elevate the well-being of everyone we touch. #teamMHSflorida

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. As we continue to grow, as one QuidelOrtho we are seeking a Scientist I to support our Immunohematology products. This person will be responsible for testing raw materials, in process bulk testing on Immunohematology products. This person will assure compliance with company standards and applicable regulatory agencies. You will be responsible to participate in failure investigations to help determine root cause, track and trend data, identify and suggest process improvements to improve business measures. This is an onsite position located in Pompano Beach Florida. Work Schedule: First Shift/ Flexible : * This will be a First shift position with flexibility to work weekends, over time and fluctuation on start time (a couple of hours earlier or later) to accommodate business needs. Strong preference for candidates demonstrating flexibility in working any shift (day and night shifts plus weekends), over time and fluctuation on start time to accommodate business needs. * Organizes and performs product release, stability and raw material testing under direct supervision. * Performs testing within established timelines and in accordance with current specifications. * Documents results clearly and accurately. Interprets results by complying to appropriate specification requirements. * Perform data trending of critical product, process information and release test results to be used in SPC/ trend analysis. * Maintains sufficient inventories off reagents and supplies. * Assures compliance to company procedures, GMP, FDA, Safety and ISO regulations in all functions. * Participate in laboratory investigations, technology transfer, validation and R&D projects. * Performs additional work-related duties as assigned. * Bachelor's degree in Medical Technology, Clinical laboratory Science, Biology, Chemistry or related field of study. * Associates in Medical Technology is acceptable. * Knowledge and experience with Good Manufacturing Practices (GMP) * Proficiency with Microsoft Office Suite of products * Knowledge and experience with Good Documentation Practices (GDP) * Pipetting * Perform Indirect Antiglobulin Testing (IAT) * Perform Direct Antiglobulin Testing (DAT) * Grading Blood Bank reactions * Perform Instrument maintenance * Perform titrations * Quality Control * Reverse Blood grouping * Blood Bank Tube Testing * Blood Bank Instrument Testing * Internal Partners: Strong working relationships with the site's Material Management, Quality, Upstream Formulation, EHS, Facilities, Engineering, Product Support are necessary to drive effective prioritization and collaboration to meet the needs of the business * External Partners: Suppliers The work environment characteristics are representative of an office, laboratory and manufacturing environment. Flexible work hours to meet project deadlines and support of operational goals. Position requires ability to flexibly spend time on the desk, analyzing data, in meetings as well as hand-on product testing as needed. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Position requires use of Personal Protective Equipment as posted. Manual dexterity to handle instruments, complete repetitive motions, and stand for long periods of time is required. Including sitting, standing, walking, bending, squatting, balancing (Maintaining body equilibrium to prevent falling when walking, standing or crouching on narrow, slippery or erratically moving surfaces. Amount and kind of balancing exceeds that needed for ordinary locomotion and maintenance of body equilibrium), and ability to lift up to 30lbs. QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at ___. #LI-SP1

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. As we continue to grow as QuidelOrtho, we are seeking a Scientist III, Quality Control. The Scientist III will be responsible for performing a variety of tests in support of testing and release of raw materials, intermediates and finished product. Works to achieve operational targets with significant impact on departmental results. Responsible for making improvements of processes, systems or products to enhance performance of technical job area. This position is in Pompano Beach Florida. * Perform in-process, final product, stability and raw material testing using both automated and manual testing methods. * Understands how this testing directly impact our customers and patients. * Trains employees. * Performs data/documentation reviews. * Will lead key quality system activities for the lab as assigned (e.g. stability and/or standards programs, equipment calibration, track and trending of quality data, etc.). * Perform other work-related duties as assigned. Required: * Bachelor of Science degree in Medical Technology, Biology, Chemistry or related field of study and minimum 5-yrs experience * Manual dexterity to handle instruments, repetitive motions and standing for long periods of time. * Excellent oral and written communication skills. * Basic knowledge of Microsoft Office suite of products (Excel, Word, Outlook). * Ability to prioritize and handle multiple tasks and challenges at the same time. * Work independently and within a team environment. Preferred: * Knowledge of Immunohematology theory and practice. * Familiarity with FDA, OSHA, ISO, cGMP * Strong preference for candidates demonstrating flexibility in working any shift (day and night shifts plus weekends) Internal: Manufacturing, Formulations, Microbiology, Quality Assurance, Quality Engineering, Product Support External: Instrument/laboratory equipment support/personnel * Weekends and Overtime may be required * FDA licensed biologics manufacturing facility. * Works primarily in laboratory setting. * Manual dexterity to handle instruments, repetitive motions and standing for long periods of time. Must be able to lift a maximum of 35 lbs. QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at ______. #LI-SP1

Job Description Ready to Make a Difference in Fitness? Do you thrive on discovering cutting-edge technology and techniques? Are you driven by a passion for fitness and empowering others to reach their goals? If so, we want YOU to join our team! The Exercise Coach – Davie is looking for a part-time Personal Trainer / Fitness Instructor to provide one-on-one and small group exercise sessions. This is your chance to inspire clients, help them transform their lives, and grow with a forward-thinking fitness studio. Your responsibilities will include: * Conducting initial consultations and fitness assessments. * Guiding clients through personalized exercise sessions. * Tracking and celebrating client progress. * Delivering upbeat, motivating support to keep clients engaged. * Converting prospects into clients by selling monthly and package sessions. * Reaching out to potential clients to bring them into the studio. What You Bring – Required Skills & Qualities To succeed in this role, you must already possess: * A genuine passion for health and wellness. * A dedication to creating exceptional customer experiences. * A people-first mindset—positive, patient, and energized. You LOVE working with others, building lasting connections, and bringing enthusiasm to every session. * Strong communication skills—confident in-person and on the phone, professional, and able to give clear, effective instructions. * A solid understanding of exercise science and human biology. * A valid CPR/AED certification from a nationally recognized provider (hands-on, in-person training required). Don’t have one yet? You’ll need to get certified before starting. * Availability to work Saturday mornings (7 AM – 1 PM). * Legal eligibility to work in the USA. Stand Out with These – Preferred Skills & Qualities These extras could boost your application: * Experience in sales. * A college degree in Kinesiology, Sports Science, or Nutrition. * Certification in personal training or group fitness instruction. * Background working with older adults or clients with varying limitations. * Fluency in Spanish. * Basic computer proficiency. * Flexibility to work early mornings (6 AM – 12 PM) and/or evenings (4 PM – 8 PM) Monday through Friday. Why Join Us? All team members receive comprehensive training in The Exercise Coach’s unique methods and technology before starting. Plus, you’ll enjoy a steady paycheck—compensation is never commission-based, so you’re paid for your time, whether you’re training clients or not. Ready to turn your passion into a rewarding career? Apply today and let’s help people thrive together! Company DescriptionThe Exercise Coach is a fast-growing fitness franchise with over 200 locations across the U.S. and Japan, specializing in efficient, technology-driven personal training. Using proprietary Exerbotics equipment, we deliver personalized 20-minute workouts twice a week. Our innovative methods, supportive team culture, and strong client retention set us apart, earning top rankings like Entrepreneur’s Franchise 500.The Exercise Coach is a fast-growing fitness franchise with over 200 locations across the U.S. and Japan, specializing in efficient, technology-driven personal training. Using proprietary Exerbotics equipment, we deliver personalized 20-minute workouts twice a week. Our innovative methods, supportive team culture, and strong client retention set us apart, earning top rankings like Entrepreneur’s Franchise 500.

Job Description Ready to Make a Difference in Fitness? Do you thrive on discovering cutting-edge technology and techniques? Are you driven by a passion for fitness and empowering others to reach their goals? If so, we want YOU to join our team! The Exercise Coach – Davie is looking for a part-time Personal Trainer / Fitness Instructor to provide one-on-one and small group exercise sessions. This is your chance to inspire clients, help them transform their lives, and grow with a forward-thinking fitness studio. Your responsibilities will include: * Conducting initial consultations and fitness assessments. * Guiding clients through personalized exercise sessions. * Tracking and celebrating client progress. * Delivering upbeat, motivating support to keep clients engaged. * Converting prospects into clients by selling monthly and package sessions. * Reaching out to potential clients to bring them into the studio. What You Bring – Required Skills & Qualities To succeed in this role, you must already possess: * A genuine passion for health and wellness. * A dedication to creating exceptional customer experiences. * A people-first mindset—positive, patient, and energized. You LOVE working with others, building lasting connections, and bringing enthusiasm to every session. * Strong communication skills—confident in-person and on the phone, professional, and able to give clear, effective instructions. * A solid understanding of exercise science and human biology. * A valid CPR/AED certification from a nationally recognized provider (hands-on, in-person training required). Don’t have one yet? You’ll need to get certified before starting. * Availability to work Saturday mornings (7 AM – 1 PM). * Legal eligibility to work in the USA. Stand Out with These – Preferred Skills & Qualities These extras could boost your application: * Experience in sales. * A college degree in Kinesiology, Sports Science, or Nutrition. * Certification in personal training or group fitness instruction. * Background working with older adults or clients with varying limitations. * Fluency in Spanish. * Basic computer proficiency. * Flexibility to work early mornings (6 AM – 12 PM) and/or evenings (4 PM – 8 PM) Monday through Friday. Why Join Us? All team members receive comprehensive training in The Exercise Coach’s unique methods and technology before starting. Plus, you’ll enjoy a steady paycheck—compensation is never commission-based, so you’re paid for your time, whether you’re training clients or not. Ready to turn your passion into a rewarding career? Apply today and let’s help people thrive together! Company DescriptionThe Exercise Coach is a fast-growing fitness franchise with over 200 locations across the U.S. and Japan, specializing in efficient, technology-driven personal training. Using proprietary Exerbotics equipment, we deliver personalized 20-minute workouts twice a week. Our innovative methods, supportive team culture, and strong client retention set us apart, earning top rankings like Entrepreneur’s Franchise 500.The Exercise Coach is a fast-growing fitness franchise with over 200 locations across the U.S. and Japan, specializing in efficient, technology-driven personal training. Using proprietary Exerbotics equipment, we deliver personalized 20-minute workouts twice a week. Our innovative methods, supportive team culture, and strong client retention set us apart, earning top rankings like Entrepreneur’s Franchise 500.

Job Description We are seeking an experienced Bilingual Senior Formulator to lead product development initiatives within a fast-paced nutraceutical/pharmaceutical manufacturing environment. This role is responsible for developing new formulations, improving existing products, and guiding a small team through the full formulation and production lifecycle. The ideal candidate is a hands-on leader with strong technical expertise in flavor systems, tablets, and nutraceutical product development. Key Responsibilities • Lead the creation, design, and optimization of flavor formulations, tablets, and other nutraceutical products., • Oversee the formulation team, providing guidance, training, and technical support., • Manage end-to-end product development, from concept through scale-up and production., • Conduct research on ingredients, raw materials, and innovative technologies to improve product performance and compliance., • Collaborate with cross-functional teams including Quality, Production, R&D, and Regulatory., • Ensure all formulations meet GMP, quality, and industry regulatory standards., • Prepare technical documentation, SOPs, and formulation records., • Bachelor's degree in a scientific field (Chemistry, Biology, Food Science, Pharmaceutical Sciences, or related)., • 5+ years of experience in nutraceutical or pharmaceutical formulation, specifically with flavors and tablets., • Proven experience developing new products and improving existing formulations., • Previous team lead or supervisory experience., • Strong understanding of GMP regulations and manufacturing standards., • Bilingual English–Spanish (required)., • Experience with supplement development, powder blends, gummies, or capsules., • Knowledge of raw material selection, stability studies, and sensory evaluation., • Project management experience.

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 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. In addition to brewing its own award-winning beers, Funky Buddha now proudly produces its own THC-infused beverages and provides co-packing services for other beverage brands. This continued expansion underscores Funky Buddha’s reputation as an innovative and fast-growing beverage producer—the first production brewery in the greater Fort Lauderdale area and the largest brewery in South Florida. “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 steps required to achieve a consistent final product ready for packaging. This includes beer, THC beverages, and co-packed products for partner brands. The Cellar Operator must be a hard-working, responsible, and self-motivated individual with a passion for craft beverages and a desire to continue learning and growing within the industry. The position requires strong mechanical aptitude, attention to detail, and the ability to multitask through different processes in a fast-paced and constantly evolving environment. EXAMPLE OF DUTIES: ESSENTIAL FUNCTIONS • Perform cellaring duties including fermentation management for beer, THC beverages, and co-packed products., • Assistance with yeast handling and management., • Execute CIP (clean-in-place) of brewing, fermentation, and beverage processing tanks and equipment., • Operate centrifuge and plate filter for product clarification., • Carefully execute treatment and conditioning plans for specialty and infused beverages., • Maintain accurate records from fermentation through finishing and packaging stages., • Follow SOPs for all products, ensuring consistent quality across Funky Buddha and co-packed brands., • Operate flash pasteurizer and related processing systems., • Maintain sanitary practices in all aspects of beverage processing., • Perform preventive maintenance on brewhouse and cellar equipment., • Assist with lab testing, sensory panels, and quality assurance activities., • Prepare, fill, and transfer beer and other beverages to and from barrels and tanks as needed., • Support cross-departmental production needs, including THC production and co-packing runs. 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. 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 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 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. 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.

Job Description We are seeking an experienced Bilingual Senior Formulator to lead product development initiatives within a fast-paced nutraceutical/pharmaceutical manufacturing environment. This role is responsible for developing new formulations, improving existing products, and guiding a small team through the full formulation and production lifecycle. The ideal candidate is a hands-on leader with strong technical expertise in flavor systems, tablets, and nutraceutical product development. Key Responsibilities • Lead the creation, design, and optimization of flavor formulations, tablets, and other nutraceutical products., • Oversee the formulation team, providing guidance, training, and technical support., • Manage end-to-end product development, from concept through scale-up and production., • Conduct research on ingredients, raw materials, and innovative technologies to improve product performance and compliance., • Collaborate with cross-functional teams including Quality, Production, R&D, and Regulatory., • Ensure all formulations meet GMP, quality, and industry regulatory standards., • Prepare technical documentation, SOPs, and formulation records., • Troubleshoot production issues and propose corrective actions.Minimum Qualifications, • Bachelor’s degree in a scientific field (Chemistry, Biology, Food Science, Pharmaceutical Sciences, or related)., • 5+ years of experience in nutraceutical or pharmaceutical formulation, specifically with flavors and tablets., • Proven experience developing new products and improving existing formulations., • Previous team lead or supervisory experience., • Strong understanding of GMP regulations and manufacturing standards., • Bilingual English–Spanish (required)., • Excellent analytical, organizational, and communication skills.Preferred Skills, • Experience with supplement development, powder blends, gummies, or capsules., • Knowledge of raw material selection, stability studies, and sensory evaluation.

Job Description Instructors are responsible for leveraging their expertise to deliver education services to students through: • Planning and organizing instructional methods and resources, • Programmatic accreditation (if applicable), • Facilitating student engagement in the classroom/learning environment, • Working one-on-one with students, • Assessing students and providing developmental feedback Position Requirements: • 2+ years of professional experience, • Master's Degree in Biology

Job Description Core Duties and Responsibilities: · Deliver accurate and continually updated information regarding Life Extension products, disease protocols, disorders, and magazine articles to LE customers. · Answer questions regarding specific product information, including product ingredients, recommended dosages and usage to Life Extension customers by phone. · Research and convey complex health-related (and scientific) information in an educated, reassuring, and professional manner while in a real-time environment. · Accept and quickly apply coaching and feedback in order to improve individual performance and customer experience. · Actively listen to our callers, utilize effective and insightful probing questions to isolate needs, while simultaneously navigating internal systems, providing accurate and complete information and documenting information for future discussions. · Periodically review basic lab results with customers making appropriate product suggestions based on the organization’s core beliefs. · Demonstrate reliability and punctuality in reporting for scheduled work. · Demonstrate flexibility as needed to meet the fluctuating business needs (i.e. overtime, delayed lunches and/or breaks). · Regular onsite attendance is an essential function of this position. · Additional duties as assigned. Position Requirements: · Bachelor's degree with a focus on Science/Health, such as Biology, Chemistry, Nutrition, Nursing, Public Health, Health Promotion or Dietary field strongly preferred · Knowledge of vitamins & supplements preferred · Advanced knowledge of online researching tools such as PubMed, Internet Explorer, etc. · Proven ability to navigate through and extract information from internal and external sites · Advanced multitasking capabilities · Requires ability to sit for prolonged periods of time

Job Description Build What Matters Most—Families, Futures, and Your Career Enjoy meaningful work while contributing to an organization that changes lives every day. US Fertility, the nation’s leading partnership of physician-led fertility practices, is redefining what it means to build a career in reproductive medicine. Our team members choose to build their career home at US Fertility because of the hope we inspire in our patients, the lives we help bring into the world, and the culture of excellence we foster across our organization. We share a deep commitment to continuously improving the patient experience and advancing research and development in one of the most dynamic and impactful fields of medicine. Through our national network of premier fertility centers—including IVF Florida—we combine clinical expertise, scientific innovation, and compassionate care. The work we do building families offers purpose, challenge, and personal reward—and we’re just getting started. Opportunity Overview We have an immediate opening for a Laboratory Administrative Assistant-Embryology to join our team at IVF Florida in Margate, Florida. In this role, the Laboratory Administrative Assistant-Embryology will: • Handle the shipping, receiving and disposition of samples, • Order and receive lab supplies, • Perform administrative duties as necessary, • Maintain a customer service oriented environment, • Make suggestions on how to reduce lab supply cost, • Maintain supply inventory by checking stock to determine inventory level, • Identify improvement opportunities and participate in resolving problems that are identified, • Attend meetings, • Communicate in an open, assertive manner at all times, • Document all patient care accurately and completely to assure communication with all members of the healthcare team We’re looking for professionals who bring both technical skill and a deep sense of responsibility to the care experience—individuals who thrive in environments where excellence, empathy, and accountability matter. Qualifications and Skills Include: • Must be locally based in South Florida, • Bachelors degree in Biology preferred, • Bilingual/Spanish speaking preferred, • Strong attention to detail, • Ability to communicate accurately and concisely, • Excellent oral and written communication, • Demonstrate motivation and flexibility What We Offer US Fertility is proud to provide a competitive, comprehensive benefits package designed to support our team members—professionally and personally—across all employment types. Full-Time Employees (30+ hours/week) • Medical, dental, and vision insurance, • 401(k) with company match, • Tuition assistance and professional development support, • Performance-based bonus opportunities, • Generous paid time off, paid holidays, and paid parental leave, • Life and disability benefits, • Fertility Discount Program, • 401(k) with company match, • Performance-based bonus opportunities, • 401(k) with company match US Fertility and its network partners believe that a diverse workforce is essential to fulfilling our mission of expanding patient access to the highest standards of fertility care. We are committed to equitable and inclusive hiring practices that ensure our clinical and operational teams reflect and support the diverse communities and patients we serve. Across our national footprint, US Fertility is a leader in offering clinical, administrative, and operational career opportunities at locations throughout the United States. We are equally committed to developing individual strengths, promoting from within, and supporting long-term career growth. This is a moment of growth, innovation, and impact. Take the next step in your career with US Fertility—and help shape the future of fertility care.

Job DescriptionSUN NUTRACEUTICALS Sun Nutraceuticals is a growing manufacturer of dietary supplements. We are seeking a reliable & motivated Quality Inspector to join our team. If you have a strong work ethic, a positive attitude, and a willingness to learn, this is an excellent opportunity to grow with a company that values hard work and promotes from within. POSITION SUMMARY The Quality Inspector is responsible for performing in-process and finished product inspections throughout the dietary supplement manufacturing facility. This role ensures all products are manufactured in compliance with current Good Manufacturing Practices (cGMP) as outlined in 21 CFR Part 111. The Quality Inspector plays a critical role in maintaining product quality, safety, and regulatory compliance. ESSENTIAL DUTIES & RESPONSIBILITIES • Conduct in-process inspections during manufacturing and packaging operations to ensure adherence to batch records and standard operating procedures (SOPs)., • Perform visual and physical inspections of incoming raw materials, in-process intermediates, and finished products for quality, and compliance with specifications., • Verify line clearances and room clearances prior to the start of each production run to prevent cross-contamination., • Review and verify batch production records, labels, and packaging materials for accuracy and completeness., • Collect and submit samples for laboratory testing, including identity, potency, purity, and microbiological analysis., • Initiate and support investigations for out-of-specification (OOS) results & deviations., • Monitor environmental conditions (temperature, humidity) and sanitation practices within production areas., • Verify that equipment calibration, cleaning, and maintenance records are current and complete., • Communicate quality issues and trends to production staff and QA management in a timely manner.QUALIFICATIONS & REQUIREMENTSEducation, • High school diploma or GED required., • Associate’s degree or coursework in a scientific discipline (Biology, Chemistry, Food Science, or related field) preferred.Experience, • 0–2 years of experience in a quality or manufacturing within a cGMP-regulated environment preferred., • Dietary supplement, pharmaceutical, or food manufacturing experience is a plus.Knowledge & Skills, • Basic understanding of cGMP regulations under 21 CFR Part 111 (training provided)., • Strong attention to detail and ability to follow written procedures accurately., • Effective written and verbal communication skills for documentation and reporting., • Ability to work independently and collaboratively in a fast-paced manufacturing environment.PHYSICAL REQUIREMENTS & WORKING CONDITIONS, • Ability to stand and walk for extended periods (up to 8 hours per shift)., • Ability to lift and carry up to 40 lbs., • Work is performed on the manufacturing floor; exposure to powders, capsules, and cleaning agents is expected., • Must be able to wear required personal protective equipment (PPE), including hairnets, gloves, safety glasses, and steel-toed shoes. 6tJZGEPZ6j

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 Description Build What Matters Most—Families, Futures, and Your Career Enjoy meaningful work while contributing to an organization that changes lives every day. US Fertility, the nation’s leading partnership of physician-led fertility practices, is redefining what it means to build a career in reproductive medicine. Our team members choose to build their career home at US Fertility because of the hope we inspire in our patients, the lives we help bring into the world, and the culture of excellence we foster across our organization. We share a deep commitment to continuously improving the patient experience and advancing research and development in one of the most dynamic and impactful fields of medicine. Through our national network of premier fertility centers—including IVF Florida—we combine clinical expertise, scientific innovation, and compassionate care. The work we do building families offers purpose, challenge, and personal reward—and we’re just getting started. Opportunity Overview We have an immediate opening for an Embryologist to join our team at IVF Florida in Margate, Florida. In this role, the Embryologist will: Clinical and Technical Standards • Perform the following aspects of Assisted Reproductive technology (ART) procedures including but not necessarily limited to: oocyte retrieval, sperm preparation for insemination, in-vitro fertilization (IVF), fertilization check, embryo evaluation, selection of embryos for transfer and vitrification, embryo vitrification, embryo thawing, embryo transfer, surgical sperm retrieval and processing, cell to tube transfer of embryo biopsy material, micromanipulation, ICSI, assisted hatching, embryo biopsy, • Prepare embryo culture dishes and solutions required for ART procedures using sterile tissue culture techniques, • Perform embryology and andrology proficiency testing required by CAP-approved agency (ABB, CAP), • Assure proper sample collection, delivery and identification, including PGT samples for release, • Perform safe handling of specimens by following the safety guidelines for biohazardous, infectious and toxic substances in the IVF laboratory, • Document quality assurance activities including description of unusual incidents, problems, and appropriate corrective action, • Perform daily/weekly quality control for procedures and equipment used in the IVF Laboratory, • Prepare semen specimens for intrauterine inseminations (IUIs), • Perform all aspects of reproductive tissue (sperm, oocyte and embryo) cryopreservation/vitrification including sample identification, inventories, checks of serology screening, freezing and thawing procedures, • Maintain laboratory records, reports, quality assurance data and assist in preparation of SART, Artworks, and Cryomodule data, • Assist in the preparation of data for clinical meetings, • Operate laboratory equipment including laminar flow hoods, microscopes, centrifuges, analytical balance, pH meter, • Set up, calibrate and clean laboratory equipment and glassware, and assure routine maintenance and repairs are performed and documented, • Attend monthly IVF laboratory meetings and periodic staff meetings, • Assist in research projects under the IVF Laboratory Director’s supervision, • Assist in training and assigning work to junior IVF support staff, • Communicate with center personnel, medical staff, patients and outside resources to ensure high quality patient care, • Assist laboratory personnel in performing laboratory services in accordance with Federal, State and local laws and guidelines to ensure laboratory maintains accreditation, • Assist as required in maintaining laboratory operations in conformity with OSHA and CLIA ‘88 regulations, • Must meet CLIA ‘88 requirements of education and experience for General Supervisor or Technical Supervisor, • Must be thoroughly familiar with Laboratory Operations Manual, • Must demonstrate skills and aptitude appropriate to the position, • Must demonstrate an ability to function effectively without direct supervision and to perform laboratory services in accord with the Laboratory Philosophy and Operating Standards We’re looking for professionals who bring both technical skill and a deep sense of responsibility to the care experience—individuals who thrive in environments where excellence, empathy, and accountability matter. Qualifications and Skills Include: • Must be a US Citizen, • Bachelor’s, Master’s, or PhD degree in biology, chemistry or the clinical laboratory/medical technology sciences from an accredited university (must have the ability to supply copies of degrees, transcripts, and references), • 1 year minimum of Embryology experience required, • Ability to access, input, and retrieve information from a computer, • Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.), • Ability to work as part of a multi-disciplinary team, • Ability to communicate accurately and concisely, • Excellent interpersonal skills What We Offer US Fertility is proud to provide a competitive, comprehensive benefits package designed to support our team members—professionally and personally—across all employment types. Full-Time Employees (30+ hours/week) • Medical, dental, and vision insurance, • 401(k) with company match, • Tuition assistance and professional development support, • Performance-based bonus opportunities, • Generous paid time off, paid holidays, and paid parental leave, • Life and disability benefits, • Fertility Discount Program, • 401(k) with company match, • Performance-based bonus opportunities, • 401(k) with company match US Fertility and its network partners believe that a diverse workforce is essential to fulfilling our mission of expanding patient access to the highest standards of fertility care. We are committed to equitable and inclusive hiring practices that ensure our clinical and operational teams reflect and support the diverse communities and patients we serve. Across our national footprint, US Fertility is a leader in offering clinical, administrative, and operational career opportunities at locations throughout the United States. We are equally committed to developing individual strengths, promoting from within, and supporting long-term career growth. This is a moment of growth, innovation, and impact. Take the next step in your career with US Fertility—and help shape the future of fertility care.

Job Description Job Title: Molecular Technologist Location: Pompano Beach, FL Salary: $25-35/hour + Benefits Position Overview Lighthouse Lab Services is partnering with a growing hybrid CRO in Boca Raton, FL to identify a Molecular Technologist to join their team. This laboratory is heavily focused on molecular diagnostics, including COVID testing, women's health, infectious disease, and cancer screening assays. Key Responsibilities • Perform and oversee high-complexity testing in accordance with CLIA, CAP, and regulatory standards Lead, train, and mentor laboratory staff, including scheduling and performance oversight * Review, verify, and release patient results with a high level of accuracy * Ensure proper quality control, calibration, and maintenance of laboratory instrumentation * Assist in assay validation, verification, and implementation of new testing platforms * Maintain compliance with all laboratory policies, procedures, and safety standards * Partner with leadership to support operational growth and process improvement initiatives Molecular & Microbiology Focus * Perform and oversee molecular diagnostic testing using PCR and real-time PCR methodologies * Support testing across infectious disease, including Respiratory Pathogen Panels (RPP), COVID, and other viral/bacterial assays * Work with women's health panels and cancer screening assays * Apply best practices in contamination control and molecular workflow design * Assist in troubleshooting complex molecular assays and resolving technical issues * Collaborate on development, validation, and optimization of molecular tests * Support microbiology workflows as needed, including specimen processing and result interpretation Instrumentation Experience (Preferred) Hands-on experience with the following platforms is highly preferred: * Abbott diagnostic systems * Roche cobas platforms * Cepheid GeneXpert systems * BioFire FilmArray systems Qualifications * Bachelor's degree in Medical Technology, Clinical Laboratory Science, Biology, or related field * Florida Clinical Laboratory Testing Personnel License * MT (ASCP), MT (AAB), or equivalent certification * Strong background in molecular diagnostics and PCR-based testing * Experience with infectious disease, women's health, and/or oncology-related testing Salary & Benefits * Competitive salary: $25-35/hour (DOE) * Health, dental, and vision insurance * 401(k) after 6 months * Paid time off and holidays About Us: At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has more than 18 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories. It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Lighthouse Lab Services will provide reasonable accommodations for qualified individuals with disabilities. Lighthouse Lab Services |?844-914-0785?|?lighthouselabservices.com #LLS2

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. Location: Miramar, FL Schedule: Monday to Friday, 8:30 AM – 5:00 PM Pay Rate: $20–$25 per hour, based on experience Qualifications: * Bachelor's degree in Chemistry, Biology, Food Science, or a related field * At least 1 year of experience in a laboratory, formulation, R&D, or regulatory role within an FDA-regulated industry (nutraceuticals, pharmaceuticals, food, medical devices, personal care, etc.) * Ability to perform basic calculations (percentages, concentrations, unit conversions, pricing) * Bilingual (English and Spanish) Essential Functions: * 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 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 Department: Manufacturing Operations Location: Weston, FL Position Summary The Technical Process and Manufacturing Specialist is responsible for the production, optimization, and quality verification of complex finished goods and specialty materials in a regulated laboratory manufacturing environment. This role supports established batch records and standard operating procedures, performs technical calculations, prepares formulations, and ensures product performance and consistency. The position involves operation and troubleshooting of analytical instrumentation, process adjustments to maintain specifications, and execution of in vitro diagnostic (IVD) manufacturing tasks. Experience with immunoassay systems, clinical analyzers, and scientific production workflows is highly desirable. . Key Responsibilities · Write, revise, review, and support controlled documentation related to manufacturing, process improvement, and quality activities · Calibrate, maintain, troubleshoot, and operate scientific instruments, including: • pH meters, • Spectrophotometers, • Dissolved oxygen meters, • Centrifuges, • Clinical chemistry analyzers, • Immunochemistry analyzers · Perform technical calculations and apply statistical methods to support process control · Work with human and animal serum, plasma, and biological materials · Operate within a biological safety cabinet using proper aseptic technique · Execute analytical laboratory and process manufacturing tasks supporting production, development, and optimization initiatives · Comply with Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP) & SOPs · Maintain accurate, compliant approved batch record documentation within controlled systems · Collaborate cross-functionally with Manufacturing, Production, Purchasing, and QA/QC teams · Participate in troubleshooting, process improvement, and cross-functional projects · Maintain laboratory cleanliness and manage biohazardous and non-biohazardous waste · Perform additional duties as required Qualifications To perform successfully in this role, the individual must: * Execute essential duties in a regulated manufacturing environment * Interpret technical and scientific documentation * Write controlled documents, SOPs, reports, and protocols in prescribed formats * Demonstrate strong attention to detail and process discipline * Possess working knowledge of Microsoft Word, Excel, and Outlook Education & Experience * Bachelor’s degree in Chemistry, Biology, Biotechnology, Biomedical Sciences, or related technical discipline preferred * Relevant laboratory, manufacturing, or diagnostic production experience may be considered in lieu of a degree * Associate degree combined with applicable industry experience will also be considered Physical Requirements * Ability to stand for extended periods * Ability to lift and/or move up to 50 pounds occasionally * Ability to work in cold storage environments at times * Ability to work with human biological samples Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Compensation & Benefits This is a full-time, exempt position. Compensation is based on qualifications, experience, and internal equity. Occasional overtime and weekend work may be required. Benefits include: Medical, dental, and vision insurance, Company Paid Life insurance, 401(k), Paid time off Work Environment The work environment characteristics described here are representative of those encountered while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. The noise level in the work environment is typically moderate. This position requires working with human biological samples. Tasks may occasionally expose the employee to extreme cold conditions. About Us Medix Biochemica is a rapidly growing in vitro diagnostics (IVD) company with Finnish roots and global operations. We operate across multiple international locations: • Espoo, Finland, • St. Louis, Missouri, • Weston, Florida, • Shanghai, China, • Besancon, France, • Konstanz, Germany We develop, produce, and supply high-quality IVD raw materials that enable customers worldwide to deliver accurate results to billions of patients. Our recent strategic acquisitions have expanded our portfolio, making us one of the most comprehensive raw material partners in the global IVD industry. With more than 250 colleagues worldwide, our values guide everything we do: We Care. We Dare. We Deliver.