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Job DescriptionDescription: Scope of Function: The Bioprocess Specialist position reports to the Upstream Manufacturing, Manager. Prior experience in GMP manufacturing, operation of GMP process equipment and aseptic technique are prerequisites. This role is responsible for supporting the overall Upstream GMP process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase 1/11/111 and commercial GMP manufacturing. Specific Duties: • Operates pharmaceutical manufacturing equipment such as: incubators, wave reactors, single-use and stainless-steel bioreactors, single use mixers, depth filtration skids, TFF skids, chromatography skids and in process testing equipment., • Executes all Upstream Clinical Manufacturing and Development operations, including but not limited to work functions in cell culture, cell banking, media optimization, seed train preparation, bioreactor operations, harvest/clarification, and technology transfer to manufacturing., • Demonstrates, understands, and adheres to Goodwin Biotechnology policies, GMP standards and safety procedures., • Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulation., • Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulations., • Supports the development of batch records, SOP’s and protocols as required., • Supports other manufacturing processes teams and other GBI groups as necessary to achieve manufacturing goals. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice. Requirements: Education and Experience Required: • BS degree in Science or Engineering., • Associate degree in science or engineering, or related field and minimum of 3 years of experience with biologic production processes under GMP compliance. Downstream experience preferred., • Minimum of High School Diploma or equivalent and 3 years of experience with biologic production processes under GMP compliance. Upstream experience preferred., • Excellent documentation skills including comprehension and review & establishing batch production records.

Job DescriptionDescription: Scope of Function: The Maintenance Technician maintains and repairs equipment, systems, and facilities within a regulated environment to ensure compliance with Good Manufacturing Practices (GMP). Key responsibilities include performing preventive maintenance, troubleshooting mechanical, electrical, and HVAC issues, meticulously documenting activities, adhering to safety and hygiene protocols, and collaborating with Quality and Operations teams to guarantee the safety, quality, and efficacy of products Specific Duties: · Conduct daily facility walk-throughs to verify the operational condition of critical areas and equipment. · Undertake PMs in accordance with the monthly PM plan for facilities, equipment, HVAC, and utility systems. · Undertake unplanned maintenance in accordance with issued work orders for equipment and utility systems. · Manage external contractor(s) to undertake unplanned maintenance in accordance with issued work orders for equipment, utility, and HVAC systems (where work cannot be undertaken in house). · Ensure materials, consumables and spare parts are prepared in advance to allow PMs to be undertaken in accordance with the monthly PM plan and the annual shutdown plan. · Ensure all documentation (including but not limited to PM, annual shutdown, work order, and investigations) is complete in a timely manner and uploaded to our Quality Management System (QMS) in accordance with the requirements. · Upload documentation, populate relevant fields and close activities in our Quality Management System (QMS). · Assist in equipment, utility, and HVAC system investigations / corrective actions and ensure completion of documentation in accordance with the requirements of the Quality Management System. · Maintain training in accordance with the Quality Management System. · Ensure all mechanical spaces, mezzanines and ceiling spaces are appropriately finished, dust free, neat, and organized with no unauthorized / improper storage of equipment, materials, consumables and / or spare parts. · Support facility construction activities. · Work as a member of the emergency response team addressing equipment malfunctions, alarms generated by the environmental monitoring system and assisting in hurricane readiness activities. · Ability to lift up to 55Lbs. Other duties as assigned. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice. Requirements: · High School Diploma. Associate Degree in Engineering is preferred. · A minimum of seven (7) years of experience in GMP Pharmaceutical/Biotech environment required. · Must have experience working in a cleanroom environment · Sufficient computer skills including experience with a Quality Management System (QMS) and Computerized Maintenance Management System (CMMS) · Good mechanical, hands-on, and excellent documentation skills. · Experienced with various Control Systems (BAS/BMS, PLC, HMI) Technical certification (EPA 608 or other HVAC certifications or CEST or CMRT or NCCER)

Job Description We are seeking a detail-oriented and proactive Bilingual Shipping Clerk to join our logistics team. This role plays a critical part in coordinating shipments, ensuring accurate documentation, and supporting smooth warehouse and transportation operations. The ideal candidate will be bilingual, have experience in logistics or supply chain management, and thrive in a fast-paced manufacturing environment. Minimum Qualifications * High school diploma or GED required; coursework or training in supply chain, operations, or logistics preferred * Experience in inventory management or warehouse logistics * Proficient in Microsoft Office, especially Excel and Word; experience with databases a plus * Strong communication and interpersonal skills * Excellent organizational and administrative capabilities * Strong attention to detail and analytical skills * Customer service-oriented mindset * Bilingual (English and Spanish) required * Background in a regulated industry such as pharmaceuticals, engineering, or healthcare is a plus Key Responsibilities * Coordinate daily shipments with brokers and transportation providers to ensure timely delivery * Communicate closely with internal and external customers to align shipment pick-up schedules * Prepare and generate accurate packing lists and shipping documentation in accordance with customer specifications * Track shipments and resolve inventory or shipping discrepancies as needed * Ensure compliance with quality standards and shipping requirements * Maintain accurate records of inventory movements and support audits * Collaborate with the logistics, sales, and manufacturing teams to fulfill orders correctly and efficiently * Respond promptly to customer and internal inquiries, providing timely updates on shipment status * Support continuous improvement efforts to enhance operational efficiency and reduce costs * Perform additional duties as assigned by the supervisor What We Offer * A team-oriented work environment in a growing pharmaceutical company * Opportunities for cross-departmental collaboration and skill development

Job Description We are seeking a detail-oriented and proactive Shipping Clerk to join our logistics team. This role plays a critical part in coordinating shipments, ensuring accurate documentation, and supporting smooth warehouse and transportation operations. The ideal candidate will be bilingual, have experience in logistics or supply chain management, and thrive in a fast-paced manufacturing environment. Minimum Qualifications * High school diploma or GED required; coursework or training in supply chain, operations, or logistics preferred * Experience in inventory management or warehouse logistics * Proficient in Microsoft Office, especially Excel and Word; experience with databases a plus * Strong communication and interpersonal skills * Excellent organizational and administrative capabilities * Strong attention to detail and analytical skills * Customer service-oriented mindset * Bilingual (English and Spanish) required * Background in a regulated industry such as pharmaceuticals, engineering, or healthcare is a plus Key Responsibilities * Coordinate daily shipments with brokers and transportation providers to ensure timely delivery * Communicate closely with internal and external customers to align shipment pick-up schedules * Prepare and generate accurate packing lists and shipping documentation in accordance with customer specifications * Track shipments and resolve inventory or shipping discrepancies as needed * Ensure compliance with quality standards and shipping requirements * Maintain accurate records of inventory movements and support audits * Collaborate with the logistics, sales, and manufacturing teams to fulfill orders correctly and efficiently * Respond promptly to customer and internal inquiries, providing timely updates on shipment status * Support continuous improvement efforts to enhance operational efficiency and reduce costs * Perform additional duties as assigned by the supervisor What We Offer * A team-oriented work environment in a growing pharmaceutical company * Opportunities for cross-departmental collaboration and skill development

Job Description Job Title: Maintenance Mechanic Company Description: Our client, a leading nutraceutical pharmaceutical manufacturer, is seeking a skilled and innovative Production Maintenance Mechanic to play a key role in optimizing manufacturing processes and ensuring product quality. • Responds to service requests as needed utilizing resources to effectively repair and ensure the safety and availability of the company systems and equipment., • Performs the job function in compliance with safety, health, environmental, and governmental regulations., • Supports Production with machine setups as needed to accomplish daily goals., • Ensures the plant is clean and free of debris or clutter., • Operates, adjusts, and performs maintenance on packaging equipment, such as: tablet counters, conveyors, printers, cartoners and other equipment to ensure compliance with established guidelines and procedures., • Performs record keeping functions (CMMS) such as documenting maintenance work performed, recording unusual operating conditions., • Performs various types of tests on mechanical and electrical equipment (Amperage, Volts, resistance)., • Contributes to the efficiency of the department by offering suggestions and participating as an active member of the team to accomplish team unit goals, objectives, and activities., • Understands and learns SOPs, GMP, safety guidelines and have the ability to complete all required documentation., • Evaluates equipment and machine operations. Removes and repairs various equipment and components., • Supports installation of new equipment, • Repairs hydraulic and pneumatic assemblies., • High school diploma or general education degree (GED) required (associate degree, Trade School Certificate and/or Military Technical Training, a plus) Equivalent work experience may be substituted for technical/vocational experience (preferred)., • College or formal technical school education with demonstrated aptitude and skills in mechanical, electrical, pneumatic, and welding techniques. One to two years in a food manufacturing environment (preferred)., • 1-2 years of experience in the maintenance industry, preferably in GMP environment., • Must be Bilingual English/Spanish., • Must have legible handwriting, and the ability to perform accurate documentation., • Must have good basic math skills such as adding, subtracting, multiplying, and dividing., • Strong organizational skills, capable of following instructions, and multitasking., • Familiar with safety protocols associated with lock out/tag out., • Ability to work without close supervision and to set one's own priorities., • Proficient with computer systems.

Job Description Job Title: Industrial Maintenance Mechanic Job Description: We are seeking a skilled and experienced Industrial Maintenance Mechanic to join our pharmaceutical manufacturing team. As an integral member of our maintenance department, you will play a key role in ensuring the continuous operation and efficiency of our industrial machinery. The ideal candidate should have specific experience in industrial maintenance within the pharmaceutical manufacturing sector and possess strong mechanical aptitude. Responsibilities: • Perform routine maintenance and repairs on industrial machinery to ensure optimal functionality., • Conduct preventive maintenance tasks on equipment to minimize downtime and extend machinery lifespan., • Diagnose and troubleshoot mechanical issues in a timely and efficient manner., • Collaborate with the maintenance team to execute planned equipment upgrades and modifications., • Maintain accurate records of maintenance activities, including repairs and replacements., • Ensure compliance with safety standards and regulations during all maintenance procedures., • Monitor and order necessary spare parts and materials for equipment maintenance., • Provide support during equipment installations and commissioning., • Respond promptly to machinery breakdowns and implement effective solutions., • Proven experience as an Industrial Maintenance Mechanic in a pharmaceutical manufacturing setting., • Strong mechanical aptitude with the ability to troubleshoot and repair industrial machinery., • Proficiency in English, both written and verbal., • Understanding of industry-specific regulations and safety protocols., • Ability to work independently and as part of a collaborative maintenance team., • Excellent problem-solving skills and attention to detail., • Physical fitness and ability to lift heavy objects.

Job Description Job Title: Maintenance Mechanic Company Description: Our client, a leading nutraceutical pharmaceutical manufacturer, is seeking a skilled and innovative Production Maintenance Mechanic to play a key role in optimizing manufacturing processes and ensuring product quality. Fulltime Monday - Friday 6am - 2:30pm • Responds to service requests as needed utilizing resources to effectively repair and ensure the safety and availability of the company systems and equipment., • Performs the job function in compliance with safety, health, environmental, and governmental regulations., • Supports Production with machine setups as needed to accomplish daily goals., • Ensures the plant is clean and free of debris or clutter., • Operates, adjusts, and performs maintenance on packaging equipment, such as: tablet counters, conveyors, printers, cartoners and other equipment to ensure compliance with established guidelines and procedures., • Performs record keeping functions (CMMS) such as documenting maintenance work performed, recording unusual operating conditions., • Performs various types of tests on mechanical and electrical equipment (Amperage, Volts, resistance)., • Contributes to the efficiency of the department by offering suggestions and participating as an active member of the team to accomplish team unit goals, objectives, and activities., • Understands and learns SOPs, GMP, safety guidelines and have the ability to complete all required documentation., • Evaluates equipment and machine operations. Removes and repairs various equipment and components., • Supports installation of new equipment, • Repairs hydraulic and pneumatic assemblies., • High school diploma or general education degree (GED) required (associate degree, Trade School Certificate and/or Military Technical Training, a plus) Equivalent work experience may be substituted for technical/vocational experience (preferred)., • College or formal technical school education with demonstrated aptitude and skills in mechanical, electrical, pneumatic, and welding techniques. One to two years in a food manufacturing environment (preferred)., • 1-2 years of experience in the maintenance industry, preferably in GMP environment., • Must be Bilingual English/Spanish., • Must have legible handwriting, and the ability to perform accurate documentation., • Must have good basic math skills such as adding, subtracting, multiplying, and dividing., • Strong organizational skills, capable of following instructions, and multitasking., • Familiar with safety protocols associated with lock out/tag out., • Ability to work without close supervision and to set one’s own priorities., • Proficient with computer systems.

Job DescriptionMaintenance Technician – GMP Environment Plantation Florida | Full-Time Permanent | No Sponsorship AvailableWe are seeking an experienced Maintenance Technician to join a regulated GMP pharmaceutical/biotech environment. The successful candidate will maintain and repair equipment, systems, and facilities while ensuring compliance with Good Manufacturing Practices (GMP).This role is hands-on, highly technical, and critical to supporting facility operations, quality, and product safety.Key Responsibilities • Perform daily facility walk-throughs to verify operational condition of critical areas and equipment., • Execute preventive maintenance (PMs) on facilities, equipment, HVAC, and utility systems per monthly schedules., • Troubleshoot and perform unplanned maintenance for mechanical, electrical, HVAC, and utility systems., • Manage external contractors for maintenance and repairs when required., • Prepare spare parts, consumables, and materials for PM and shutdown activities., • Complete and upload documentation into the Quality Management System (QMS) and CMMS in a timely manner., • Participate in equipment/utility/HVAC investigations and corrective actions., • Maintain compliance with training requirements within the QMS., • Support facility construction activities and serve on the emergency response team (equipment malfunctions, alarms, hurricane readiness, etc.)., • Ensure mechanical spaces and cleanroom environments are dust-free, organized, and GMP-compliant.Qualifications, • High School Diploma required; Associate Degree in Engineering preferred., • Minimum 7 years’ experience in a GMP Pharmaceutical/Biotech environment., • Direct experience working in a cleanroom environment., • Strong mechanical skills, hands-on troubleshooting ability, and excellent documentation practices., • Proficiency with QMS, CMMS, and computer-based systems., • Experience with control systems (BAS/BMS, PLC, HMI)., • Technical certifications preferred: EPA 608, HVAC, CEST, CMRT, or NCCER., • Ability to lift up to 55 lbs.

Job Description Job Title: Maintenance Mechanic Company Description: Our client, a leading nutraceutical pharmaceutical manufacturer, is seeking a skilled and innovative Production Maintenance Mechanic to play a key role in optimizing manufacturing processes and ensuring product quality. Fulltime Monday - Friday 6am - 2:30pm • Responds to service requests as needed utilizing resources to effectively repair and ensure the safety and availability of the company systems and equipment., • Performs the job function in compliance with safety, health, environmental, and governmental regulations., • Supports Production with machine setups as needed to accomplish daily goals., • Ensures the plant is clean and free of debris or clutter., • Operates, adjusts, and performs maintenance on packaging equipment, such as: tablet counters, conveyors, printers, cartoners and other equipment to ensure compliance with established guidelines and procedures., • Performs record keeping functions (CMMS) such as documenting maintenance work performed, recording unusual operating conditions., • Performs various types of tests on mechanical and electrical equipment (Amperage, Volts, resistance)., • Contributes to the efficiency of the department by offering suggestions and participating as an active member of the team to accomplish team unit goals, objectives, and activities., • Understands and learns SOPs, GMP, safety guidelines and have the ability to complete all required documentation., • Evaluates equipment and machine operations. Removes and repairs various equipment and components., • Supports installation of new equipment, • Repairs hydraulic and pneumatic assemblies., • High school diploma or general education degree (GED) required (associate degree, Trade School Certificate and/or Military Technical Training, a plus) Equivalent work experience may be substituted for technical/vocational experience (preferred)., • College or formal technical school education with demonstrated aptitude and skills in mechanical, electrical, pneumatic, and welding techniques. One to two years in a food manufacturing environment (preferred)., • 1-2 years of experience in the maintenance industry, preferably in GMP environment., • Must be Bilingual English/Spanish., • Must have legible handwriting, and the ability to perform accurate documentation., • Must have good basic math skills such as adding, subtracting, multiplying, and dividing., • Strong organizational skills, capable of following instructions, and multitasking., • Familiar with safety protocols associated with lock out/tag out., • Ability to work without close supervision and to set one’s own priorities., • Proficient with computer systems.

Job Description We are seeking an experienced Maintenance Technician to join our team and support the maintenance and repair of industrial production and packaging equipment. The ideal candidate will bring a strong mechanical and electrical background, with hands-on experience in troubleshooting, repairing, and maintaining pharmaceutical or packaging machinery. This role requires someone who is proactive, resourceful, and able to work both independently and in a team environment. MUST BE BILINGUAL ENGLISH AND SPANISH. Location: Davie, FL Schedule: Monday – Friday, 10:00 PM – 5:45 AM (Overnight Shift) Salary: $28.00 per hour Key Responsibilities • Perform minor electrical duties including voltage checks, continuity checks, and replacement of electrical components., • Disassemble, repair, and replace malfunctioning components of machinery and equipment., • Conduct troubleshooting, repairs, and preventive maintenance on industrial production and processing machinery., • Maintain and document preventive maintenance schedules for all machinery and equipment., • Troubleshoot, repair, and replace conveyor belts, bearings, and electrical motors., • Assemble and reassemble machinery and equipment using hand tools and pneumatic power tools., • Request necessary parts and electrical components to keep equipment operational., • Interpret and follow mechanical diagrams, blueprints, and schematic drawings., • High School Diploma or equivalent required., • 5+ years of experience as a maintenance mechanic/technician in a packaging or industrial environment (pharmaceutical experience preferred)., • Strong knowledge of mechanical, electrical, pneumatic, hydraulic, and welding systems., • Hands-on experience with A/DC motors, PLC electronic systems, and machinery installations., • Skilled in reading and interpreting diagrams, blueprints, and schematics., • Forklift operation experience required., • Experience repairing industrial pharmaceutical equipment., • Bilingual (English/Spanish)., • Must be highly resourceful, responsible, and hardworking with the ability to work independently.

Job Description Salary: $15 - $18/hour We Are Hiring Pharmaceutical Machine Operators For a company in the pharmaceutical/nutraceutical industry. The ideal candidate will have experience operating machinery in the manufacturing of vitamins and supplements. Responsibilities: • Set up machines for production, • Feed the machine with the appropriate powder, • Verify proper release of capsules, • Monitor weight variations and recover powder from vacuum systems, • Supply raw materials (powder and capsules) as needed, • Complete batch records accurately and on time, • Keep the work area clean and in compliance with safety standardsRequirements:, • High school diploma or equivalent, • Attention to detail and basic math skills, • Previous experience in pharmaceutical/nutraceutical manufacturing (preferred), • Bilingual (English and Spanish) preferred, • Ability to stand, bend, lift, push, and move drums weighing 50 to 100 kg with assistance, • Able to use ladders when necessary

Job DescriptionAbout Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. • Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs, • Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Key Responsibilities: • Handle initial outreach and inquiries from potential clients via phone, email, and other channels., • Collect and document detailed client information and needs., • Accurately input and update client data in the company CRM in a timely manner., • Qualify leads and refer them to Client Service and Account Managers for follow-up., • Maintain clear and timely communication with clients throughout the intake process., • Collaborate with sales and marketing teams to align outreach efforts., • Provide administrative support related to client management activities., • Excellent command of English; Spanish language skills are a plus., • Up to 1-2 years of experience in sales, customer service, or commercial support roles., • Strong communication skills and a customer-oriented mindset., • Detail-oriented with strong accuracy in data entry and management., • Ability to work effectively in a team and manage priorities in a fast-paced environment., • Interest in pharmaceutical or healthcare industries is desirable but not required., • Availability to work 44 hours per week, Monday through Friday, onsite. This is a full-time position, working 44 hours per week, Monday through Friday This is a 100% onsite role; remote or hybrid work is not available Pay Range$60,000—$70,000 USD Benefits: • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.

Job Description Essential Functions and Responsibilities: • Set the machine (operator with the most experience), • Refill or supply the machine with raw material powder as necessary, • Fill out all the different formats, based on the time established, • Keep the work area clean., • Follow established SOPs for position and comply with GMPs, • High School diploma or equivalent, • Detail oriented, • Manufacturing or pharmaceutical/nutraceutical experience preferred Requires frequently standing, bending, lifting, 50lbs and pushing, pulling, 100 kg drums with powder; using ladders. Typical Work Conditions: • Person will be subject to food and nutritional bulk ingredients, which may affect the respiratory system or the skin, including an environment subject to odors, dust or airborne allergens., • Person will be working in a dry and low moisture environment and will have exposure to normal work hazards, including a variety of physical conditions such as a proximity to moving mechanical parts.

Position Purpose: A staff pharmacist in a hospital setting prepares and dispenses medications, reviews patient charts, monitors therapy and collaborates with other healthcare professionals to optimize medication use and patient care. What you will do: Full Time Pharmacist: Week-Ends (3-12hr nights): Friday-Saturday-Sunday (7pm-7:30am) $10,000 Sign on Bonus · Medication Dispensing and Preparation: Accurately preparing, compounding, and dispensing medications and other pharmaceutical supplies to fill prescriptions. · Patient Care: Reviewing patient charts, monitoring and adjusting medication therapy, and counseling patients on the correct use of medications and potential side effects. · Collaboration: Working closely with physicians, nurses, and other healthcare providers to make informed medication decisions and ensure optimal patient outcomes. · Pharmacy Management: Contributing to the hospital's formulary (list of approved drugs), managing medication inventory, and overseeing support staff. · Compliance and Safety: Adhering to regulations, maintaining required aseptic procedures in sterile product preparation areas, and ensuring drug quality and safety. Minimum Qualifications: • Graduate of an accredited School of Pharmacy with a minimum of a Bachelor's degree; Pharm D is preferred. • Previous experience as a Pharmacist in a hospital setting is preferred. Licensure: • Current Florida Pharmacy License Position Highlights and Benefits • Comprehensive benefit packages available, including medical, dental, vision, paid time off, 403B, and education assistance., • We serve together in the spirit of the Gospel as a compassionate and transforming healing presence within our communities., • We live and breathe our guiding behaviors: we support each other in serving, we communicate openly, honestly, respectfully, and directly, we are fully present, we are all accountable, we trust and assume goodness in intentions. Ministry/Facility Information: • Holy Cross Hospital in Fort Lauderdale, Florida is a full-service, non-profit Catholic hospital, sponsored by the sisters of Mercy and a member of Trinity Health., • We are committed to providing compassionate and holistic person-centered care., • We are the only Catholic hospital in Broward and Palm Beach counties and are not for profit. We are part of Trinity Health, one of the largest multi-institutional Catholic health care delivery systems in the nation. Together, we serve people and communities in 21 states from coast to coast, providing nearly 2.8 million visits annually., • Comprehensive benefits that start on your first day of work, • Retirement savings program with employer matching Legal Info We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

Essential Functions and Responsibilities: • Evaluates the chemical and physical properties of various substances, • Follows the instructions and pre-established guidelines to perform the functions of the job, • Responsible for routine chemical analysis work and reviewing involving pharmaceutical raw materials, process intermediates and finished products following GMPs, • Prepare volumetric test solutions and mobile phases, • Utilize knowledge of High-Performance Liquid Chromatography (HPLC), Inductively Coupled Plasma (ICP), and titration techniques., • Maintains appropriate documentation (records and lab notebooks) as required by SOP’s and cGLP’s, • Audits raw data results and laboratory documentation, • Calculates, interprets and review test results. Prepare test reports and review lab notebooks, • Performs OOS investigations as described in the SOPs to establish integrity of data Phase I & Pase II), • Operates, maintains, calibrates and qualifies equipment in assigned areas, • Able to write and execute protocols with minimum supervision and SOPs, • Assist in investigations, development and validation to method development., • Disposes waste according to Environmental Protection Agency (EPA) regulations and transfer of gas cylinders, • Follows laboratory safety rules, • Assists in the process of methods development, • Other duties as assigned by the immediate Supervisor Qualifications: • Bachelor’s degree in Chemist or Science discipline and/or equivalent work experience, • 1 - 3 years experience, • Bilingual (English and Spanish) preferred, • Basic use of Excel, Word and quality management systems., • Knowledge of lab equipment (HPLC, ICP-MS, GC, UV, FT NIR), • Experience and knowledge in Methods Validation, • Knowledge in GMP regulations and safety practices, • Knowledge of GLP practices.

About the Company: Celltrion USA is Celltrion’s U.S. subsidiary established in 2018. Headquartered in New Jersey, Celltrion USA is committed to expanding access to biologics to improve care for U.S. patients. Celltrion USA will continue to leverage Celltrion’s unique heritage in biotechnology, supply chain excellence, and best-in-class sales capabilities to improve access to high-quality biopharmaceuticals for U.S. patients. Celltrion Healthcare, which suggested a new growth model in the Korean biopharmaceutical industry through biosimilars, is now advancing to new challenges to become a global pharmaceutical provider. Just as it has overcome many obstacles in the past, Celltrion Healthcare will successfully pave the path for global direct selling, which has never been achieved yet by Korean biopharmaceutical companies. As it continues to surpass its current success, Celltrion Healthcare will take a leap forward to become a leading global biopharmaceutical company. Celltrion Healthcare provides biosimilar and innovative biopharmaceutical medications to help increase patient access to advanced therapies around the world. POSITION SUMMARY Reporting to the ISL Immunology Sales Lead, the Celltrion Immunology Specialist (CIS) is responsible for achieving the sales objectives and revenue target for their territory. They accomplish this through engaging Healthcare Professionals (HCPs) in field interactions to promote assigned product(s), maximizing the product(s)’ selling potential and meeting program objectives. The CIS achieves this by developing and maintaining relationships with HCPs, key decision makers and achieving sales goals. The CIS achieves this by educating HCPs about product features, benefits, safety profile, and approved indications to ensure appropriate patient use. The CIS utilizes approved tools for product and program promotion and maintains a competent level of product, program, and customer activity knowledge. Covering Fort Lauderdale, Florida territory. KEY ROLES AND RESPONSIBILITIES • Implement sales strategy. Drive growth of business through a concrete understanding of the assigned territory and a strategic approach to building an effective territory plan. Achieve key goals and maximize the achievement of sales objectives through proactive and strategic sales., • Create and implement territory business plans to achieve territory and business sales goals. Ensure alignment with market insights and feedback. Prepare reports for Management as needed., • Engage customers in an effective and compliant way that reflects understanding of their environment and provides insight relevant to their practice., • Demonstrate subject matter expertise with customers using effective selling, listening and negotiation skills, and approved messaging, and effectively use approved promotional aids., • Listen and respond appropriately to customer needs and questions, • Manage daily sales activity and performance according to defined expectations and complete required daily data entry of call activity in CRM., • Represent Celltrion USA with the highest level of credibility to sustain a positive impression with customers., • Participate in national, regional and district meetings, training sessions and represent Celltrion USA at national and/or local conventions when applicable., • Good understanding of and full compliance with all laws, regulations, Celltrion Code of Conduct, all privacy and data guidelines, relevant state and federal laws and regulations, and terms and conditions prescribed in the Sample Administrative Agreements and PDMA Guidelines. WORK EXPERIENCE • A minimum of 5 years of pharmaceutical sales experience required., • Immunology experience required. Track record of sales success and existing relationships with customers in immunology (specifically gastroenterology and rheumatology), • Biologics experience strongly preferred, along with working knowledge of patient HUBs, assistance programs, and specialty pharmacy. QUALIFICATIONS • High level selling, persuasion, presentation, and closing skills. Elevated levels of initiative, resilience, and drive for results. Sound decision making skills and intellectual curiosity. Top business planning skills with a winning mindset., • Ability to comprehend and communicate complex technical/medical terminology and to maintain the required technical expertise including competitive product knowledge., • Effective collaboration skills; able to work independently and as a team member., • Flexibility to embrace challenges and ability to handle multiple tasks simultaneously., • Must be 18 years of age or older with valid US driver’s license and a safe driving record., • Willingness to travel within the assigned territory and to work related meetings and functions (including overnight and/or weekends). EDUCATION Bachelor’s degree from an accredited university or college required. CORE COMPETENCIES • Communication - clear, concise, and ability to motivate; ability to articulate about the company and products, • Knowledge - understanding of product portfolio, • Collaboration - ability to communicate across functions and at all levels in the organization, • Compliance – understands industry regulations to maintain compliance Celltrion USA is an equal opportunity employer. It is our policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. #LI-DD

Inizio Engage has a long-standing partnership with Boehringer Ingelheim Pharmaceuticals to offer support for an expanding product portfolio in primary care. We are seeking a performance driven Pharmaceutical Field Sales Representative with strategic problem- solving skills, that can collaborate with multiple stakeholders. The Ideal candidate will demonstrate a track record of sales success or related experience, regardless of industry background. Pharmaceutical experience is not required. We are seeking individuals who can quickly make a meaningful impact, leveraging their proven ability to deliver results, build relationships and adapt in a dynamic environment. The Pharmaceutical Field Sales Representative will achieve sales and activity targets on assigned territories across primary care customers and meet all relevant standards as set by Inizio and Boehringer Ingelheim Pharmaceuticals leadership. This is your opportunity to join Inizio Engage and represent Boehringer Ingelheim Pharmaceuticals! What’s in it for you? * Competitive compensation * Excellent Benefits – accrued time off, medical, dental, vision, 401k, disability & life insurance, paid maternity and paternity leave benefits, employee discounts/promotions * Employee discounts & exclusive promotions * Recognition programs, contests, and company-wide awards * Exceptional, collaborative culture * Best Places to Work in BioPharma (2022, 2023, & 2024) * Certified Great Place to Work (2022, 2023, 2025) What will you be doing? * Driving demand through clinical selling and education to targeted Physicians * Establish, maintain and develop strong relationships with HCPs (includes physicians, Nurses, NP, PA, MA, etc.) * Deliver sales messaging, patient and product information to targeted HCP offices * Achieve or exceed activity targets as set by the company * Complete administrative items daily * Comply with all Boehringer Ingelheim Pharmaceuticals and Inizio policies, including compliance and ethics requirements, and trainings * Effective time management and coordination of: * Routing plans * Daily/weekly call activities * Demonstrate persistence towards accomplishing defined sales objectives * Must have a dependable automobile with insurance coverage in compliance with company guidelines. * Collaborate with geographic partners What do you need for this position? * Bachelor’s degree * Business to Business sales experience preferred * Comfort with Technology/Virtual Engagements * Ability to travel up to 20% of time as required (some territories could be more than 20%) * Overnight Travel Required * Valid driver’s license and clean driving record About Inizio Engage Inizio Engage is a strategic, commercial, and creative engagement partner that specializes in healthcare. Our passionate, global workforce augments local expertise and diverse mix of skills with data, science, and technology to deliver bespoke engagement solutions that help clients reimagine how they engage with their patients, payers, people and providers to improve treatment outcomes. Our mission is to partner with our clients, improving lives by helping healthcare professionals and patients get the medicines, knowledge and support they need. We believe in our values: We empower everyone/We rise to the challenge/We work as one/We ask what if/We do the right thing, and we will ask you how your personal values align to them. To learn more about Inizio Engage, visit us at: ___ Inizio Engage is proud to be an equal opportunity employer. Individuals seeking employment at Inizio are considered without regards to age, ancestry, color, gender, gender identity or expression, genetic information, marital status, medical condition (including pregnancy, childbirth, or related medical conditions), mental or physical disability, national origin, protected family care or medical leave status, race, religion (including beliefs and practices or the absence thereof), sexual orientation, military or veteran status, or any other characteristic protected by federal, state, or local laws. Further, pursuant to applicable local ordinances, Inizio will consider for employment qualified applicants with arrest and conviction records. Inizio Engage is an equal opportunity employer M/F/V/D. We appreciate your interest in our company, however, only qualified candidates will be considered.

Position Purpose: A staff pharmacist in a hospital setting prepares and dispenses medications, reviews patient charts, monitors therapy and collaborates with other healthcare professionals to optimize medication use and patient care. What you will do: Full Time Pharmacist: 4–10-hour shifts (Mixed Shifts) Primary Shift: 12:30pm – 11:00pm. May include every other weekend. $10,000 Sign on Bonus · Medication Dispensing and Preparation: Accurately preparing, compounding, and dispensing medications and other pharmaceutical supplies to fill prescriptions. · Patient Care: Reviewing patient charts, monitoring and adjusting medication therapy, and counseling patients on the correct use of medications and potential side effects. · Collaboration: Working closely with physicians, nurses, and other healthcare providers to make informed medication decisions and ensure optimal patient outcomes. · Pharmacy Management: Contributing to the hospital's formulary (list of approved drugs), managing medication inventory, and overseeing support staff. · Compliance and Safety: Adhering to regulations, maintaining required aseptic procedures in sterile product preparation areas, and ensuring drug quality and safety. Minimum Qualifications: • Graduate of an accredited School of Pharmacy with a minimum of a Bachelor's degree; Pharm D is preferred. • Previous experience as a Pharmacist in a hospital setting is preferred. Licensure: • Current Florida Pharmacy License Position Highlights and Benefits • Comprehensive benefit packages available, including medical, dental, vision, paid time off, 403B, and education assistance., • We serve together in the spirit of the Gospel as a compassionate and transforming healing presence within our communities., • We live and breathe our guiding behaviors: we support each other in serving, we communicate openly, honestly, respectfully, and directly, we are fully present, we are all accountable, we trust and assume goodness in intentions. Ministry/Facility Information: • Holy Cross Hospital in Fort Lauderdale, Florida is a full-service, non-profit Catholic hospital, sponsored by the sisters of Mercy and a member of Trinity Health., • We are committed to providing compassionate and holistic person-centered care., • We are the only Catholic hospital in Broward and Palm Beach counties and are not for profit. We are part of Trinity Health, one of the largest multi-institutional Catholic health care delivery systems in the nation. Together, we serve people and communities in 21 states from coast to coast, providing nearly 2.8 million visits annually., • Comprehensive benefits that start on your first day of work, • Retirement savings program with employer matching Legal Info We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

Job Description Overview PharMerica is seeking a highly capable and motivated individual to join our team. PharMerica is a non-retail pharmacy that focuses on providing exceptional customer service and meeting the pharmacy needs for hospitals, rehabilitation facilities, long-term acute care centers, and other specialized care centers nationwide. This position will provide the opportunity to grow your pharmaceutical skills under the direct guidance of a state licensed pharmacist while providing essential care to our patients in our closed-door pharmacy. Our organization is in high growth mode, which can provide opportunities for advancement for individuals looking for career progression! Schedule: Monday - Friday 8am - 5pm • Pharmacy tech license (if required by state), • National certification preferred, • Previous pharmacy experience preferred Our Benefits Include: • Competitive pay, • Shift differential, • Health, dental, & vision, • Company paid STD & LTD, • Paid Time Off, • Flexible Schedules, • Tuition Reimbursement, • 401k, • Employee Discount Program Pharmacy Technician License Fees, we’ve got your covered! New hire and current employees are eligible re reimbursement for license fees (as required). If your passion is service excellence and top-quality care, come join our team! *Position will be posted for a minimum of 7 business days Responsibilities • Fills prescription items, as permitted by the State Board of Pharmacy, packaging medications for dispensing and for delivery, meeting the accuracy and productivity standards of the pharmacy, • Labels products appropriately, including cautionary or auxiliary labels, • Participates in the periodic inventory of the pharmacy, • May check in drugs and supplies, stock shelves and remove out-of-date items from the inventory, • Prepares medications including emulsions, liquids, powders and ointments, which may include non-sterile compounding, • Communicates with internal and external customers in a pleasant and professional manner, • May process returned medications from the facility for credit or destruction, • Assists in the training of new employees, • Also performs at least one of the following:, • Works in the Controlled Drugs (Narcotics) Room;, • Works with automated machine to prepack drugs;, • Manages inventory functions such as monitoring pharmaceutical levels and identify expired medications, managing to the pharmacy standard for Days on Hand;, • Inputs patient data and medication orders into a computer system to produce labels (data entry);, • Mixes/packages IV medications, sanitizes IV room, equipment and hood, • Services facility-based medication dispensing machines (e.g., RxNow), • Performs other tasks as assigned Qualifications • Required: High School diploma or equivalent. Experience in a pharmacy setting and with medical terminology. Ability to operate a computer; ability to recognize and identify medications. Detail oriented; goal oriented, team player, effective oral communication. Pharmacy Technician license (as required by state)., • Desired: Long Term Care pharmacy experience & National Pharmacy Technician License.

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 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 Essential Functions and Responsibilities: • Evaluates the chemical and physical properties of various substances, • Follows the instructions and pre-established guidelines to perform the functions of the job, • Responsible for routine chemical analysis work and reviewing involving pharmaceutical raw materials, semi-finished goods, and finished goods according to defined specifications, • Performs a variety of laboratory techniques including sample weighing and recording preparation of standard solutions, buffers, sample preparation requiring extractions, filtration, centrifugation, pipetting, etc., • Audits raw data results and laboratory documentation, • Calculates, interprets, and reviews test results. Prepares test reports and reviews lab notebooks, • Performs OOS investigations as described in the SOPs to establish integrity of data, • Operates, maintains, calibrates and qualifies equipment in assigned areas, • Ability to write and execute protocols with minimum supervision and SOPs, • Follows laboratory safety rules, • Assists in the process of methods development, • Bachelor’s degree in Chemistry or related, • 1 - 3 years’ experience as Industrial Chemist, • Bilingual (English and Spanish), • Knowledge in lab equipment (HPLC, ICP/MS, UV, IR), • Knowledge in GMP and GLP regulations

Job Description Job Title: Industrial Chemist (2nd Shift) Location: Davie, FL Schedule: Monday to Friday, 4:15 PM – 12:45 AM Position Summary: We are seeking a motivated Industrial Chemist to join our pharmaceutical manufacturing team on the 2nd shift. The ideal candidate will have a strong background in analytical chemistry and experience working in a GMP-regulated environment. This role is responsible for performing chemical analyses on raw materials, intermediates, and finished products to ensure quality and compliance. Essential Functions & Responsibilities: • Evaluate the chemical and physical properties of various substances using analytical techniques, • Perform routine chemical analysis of pharmaceutical raw materials, intermediates, and finished products in compliance with GMP standards, • Follow pre-established protocols and SOPs to carry out lab functions accurately, • Audit raw data, results, and laboratory documentation for accuracy and completeness, • Calculate, interpret, and review test results; prepare reports and maintain detailed lab notebooks, • Conduct Out-of-Specification (OOS) investigations per SOPs to ensure data integrity, • Operate, maintain, calibrate, and qualify laboratory instruments in assigned areas, • Assist with method development and protocol execution with minimal supervision, • Adhere to all laboratory safety protocols and company policiesQualifications:, • Bachelor’s degree in Chemistry or related field, • 1–3 years of experience in a pharmaceutical manufacturing or analytical lab setting, • Bilingual in English and Spanish (preferred), • Hands-on experience with lab instruments such as HPLC, GC, UV, and IR, • Solid understanding of GMP regulations and quality systems

Job Description Location: Miramar, FL Industry: Pharmaceutical Schedule: Monday – Friday | 8:30 AM – 5:00 PM Type: Full-Time Very Attractive Opportunity! Job Description (English): We are currently seeking a detail-oriented and motivated Bilingual Purchasing Clerk to join a well-established pharmaceutical company located in Miramar, FL. This is a very attractive, full-time opportunity with a consistent Monday through Friday schedule and a professional, fast-paced work environment. Key Responsibilities: • Process purchase orders and maintain accurate purchasing records, • Communicate with suppliers to confirm order status, pricing, and delivery timelines, • Coordinate with internal departments to fulfill supply needs, • Ensure inventory levels meet production demands, • Assist in managing supplier relationships and resolving order discrepancies, • Support purchasing manager with daily administrative tasks, • Fluent in both English and Spanish (written and verbal), • 1–2 years of purchasing, procurement, or related experience (pharmaceutical or manufacturing preferred), • Strong attention to detail and organizational skills, • Proficiency in Microsoft Office (Excel, Word), • Excellent communication and negotiation skills, • Ability to work independently and as part of a team

Job DescriptionSalary: $45K-$55K Title: Mid-Market Account Executive About the Role After completing our 3-6 month training program with our Sales Trainer, you will take complete ownership of building your own book with new and or existing shipper partners. You will represent TransLoop as the main point of contact. The definitive goals in this position are to build trust, leverage TransLoops technology, carrier network and top talent to identify opportunities for new and continued partnerships with shippers, nationwide. This position will take a well-organized self-starter and all-around sales beast. We are on a mission to build the most elite sales team in the logistics industry and are always interested in bringing on top talent. This is a high-impact role for TransLoop. The success of this role will have a material impact on our business and the future growth of TransLoop. What You'll Do * Develop new and grow existing customer relationships lead generation and prospective * Build deep pipeline and qualify them as leads * Identify opportunities to improve our offerings, value proposition, and sales cadence * Leverage our leading tech platform * Design/Implement selling proposition to onboard new customers * Identify and build new sales processes * Give exceptional customer service every day What You'll Need * Relevant supply chain, sales or customer service experience * Logistics experience preferred, but not required * Exemplify a proven track record of high performance * Strong writing and speaking skills Bonus Points * Supply chain, logistics or sales-related degree * You have experience selling in 3PL, Transportation, or Tech * Experience in pharmaceutical, professional sports or any other sales role Enjoy the good life: TransLoop wants you to love where you work so we offer * Competitive compensation * Uncapped pay & competitive salaries * Medical, dental, and vision coverage (50% paid by TransLoop) * Personal financial advisor * Wellness Days About TransLoop Imagine working at a logistics company where all team members were supportive, had industry experience and the technology offerings did not look like an excel sheet Imagine having free rein on all shippers in the country and not being tied down because your company saturated the entire market Imagine carriers and shippers actually wanting to work with you Imagine all drivers tracking in real-time, eliminating annoying check calls and issues like finding out a carrier isnt going to pick up a load because he did not answer his phone. Welcome to TransLoop, a much better logistics company TransLoop is a modern digital freight network revolutionizing logistics for shippers and carriers of all sizes. The team pairs cutting-edge technology with white-glove service to deliver unparalleled transparency, industry-leading reliability, constant innovation, and real-time collaboration with every shipment. Transloop is proud to be an Equal Employment Opportunity and Affirmative Action employer. We prohibit discrimination and or/harassment of any type, including but not limited to discrimination and or harassment based upon race, religion, religious creed, color, national origin, ancestry, citizenship, sex, sexual orientation, gender, gender identity, gender expression, age, pregnancy or relation medical conditions, childbirth, breastfeeding, parental status, veteran and/or military statue, disability (physical or mental) medical condition, genetic information or characteristics, political affiliation, domestic violence survivor status, marital status, or other characteristics prohibited by federal, state, or local law. Additionally, Transloop participates in the E-Verify program in all locations. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Job Description We are seeking a detail-oriented and highly organized Regulatory Technician to join our team. This role is responsible for ensuring compliance with FDA regulations and maintaining regulatory documentation related to manufacturing, packaging, labeling, and holding operations for dietary supplements. The ideal candidate should have strong technical writing skills, regulatory knowledge, and experience in a cGMP-controlled environment. Minimum Qualifications: • Strong technical writing and verbal communication skills., • Ability to manage multiple tasks and meet deadlines., • Proficiency in MS Office (Word, Excel, PowerPoint) and ERP systems. Key Responsibilities: • Ensure compliance with FDA regulations (21 CFR Part 111) for manufacturing, packaging, labeling, and holding of dietary supplements., • Manage accreditations, certifications, licenses, and permits from federal and international agencies., • Review and determine regulatory compliance for all labeling and packaging components., • Serve as Regulatory Intelligence by staying up to date on FDA regulations and industry practices., • Prepare and maintain customer quality questionnaires., • Keep management informed of new FDA regulations and industry developments., • Work with department managers to coordinate updates to procedures and documentation., • Maintain and ensure the safe storage and inventory of labels., • Control the issuance and return of labels within the packaging department., • Coordinate and implement GMP training programs and conduct sessions when necessary., • Maintain all training documentation in accordance with company policies., • Prepare technical submissions for international product registration., • Oversee the status and maintenance of trademarks, registrations, and patents., • Perform other duties as assigned by the immediate supervisor.

Job DescriptionAbout Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. • Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs, • Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes About the Role The Pharmacy Hub (TPH) is seeking a detail-oriented Pre-PV1 Pharmacy Technician to support intake, data entry, and clinic outreach functions. As part of the verification support team, you will prepare prescriptions for PV1 pharmacist review by ensuring accuracy, resolving discrepancies, and coordinating directly with clinics for clinical edits. This role is key to maintaining efficiency, compliance, and patient safety in a high-volume mail-order environment. Responsibilities • Accurately perform dual data entry of prescription information, ensuring consistency across systems., • Identify missing, incomplete, or unclear prescription details requiring resolution before PV1., • Document communications and edits per SOPs for audit trail and compliance., • Collaborate with pharmacists, interns, and fulfillment staff to support smooth queue progression., • Active Pharmacy Technician license (CPhT preferred)., • Minimum 1 year of pharmacy experience (retail, mail-order, or telepharmacy preferred)., • Strong attention to detail with proven accuracy in data entry., • Excellent communication skills, especially in professional clinic interactions., • Familiarity with pharmacy workflow systems (DispensePro, SureScripts, or equivalent) preferred., • Competitive pay structure., • Flexible scheduling options., • Growth opportunities in a rapidly expanding telepharmacy model., • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.

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 DescriptionAbout Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. • Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs, • Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Job Summary The Financial Analyst (FP&A) supports data-informed decision-making and enhances financial performance by providing actionable insights and analysis across the organization. This role ensures the delivery of impactful analysis, forecasts, financial modeling, and monthly reporting by combining financial expertise with a deep understanding of business operations. Key responsibilities include enhancing operational efficiency, supporting financial goals, and contributing to the company's long-term success. The Financial Analyst (FP&A) collaborates with Operations, Finance, IT, and company leadership to maximize efficiency and minimize costs in alignment with strategic objectives. Key Responsibilities • Develop, maintain, and improve financial models to support forecasting, budgeting, and long-term planning., • Prepare monthly, quarterly, and annual financial reports and variance analyses for management review., • Partner with Operations, IT, and Finance to identify opportunities for cost savings, efficiency improvements, and revenue growth., • Monitor key performance indicators (KPIs) and provide actionable recommendations to support strategic decision-making., • Conduct scenario analyses and sensitivity testing to evaluate financial risks and opportunities., • Support the annual budget and reforecasting processes, ensuring alignment with strategic goals., • Assist in the preparation of presentations and reports for executive leadership and stakeholders., • Ensure accuracy, consistency, and clarity in financial reporting and data analysis. Qualifications • Bachelor's degree in Finance, Accounting, or a related field required; MBA or CPA/CFA a plus., • 2–4 years of experience in FP&A, corporate finance, or related field., • Strong financial modeling and Excel skills; experience with BI/reporting tools (e.g., Power BI, Tableau, or similar) preferred., • Knowledge of ERP systems (NetSuite, SAP, Oracle, or similar) is an advantage., • Excellent analytical, problem-solving, and critical thinking skills., • Strong written and verbal communication skills with the ability to present complex information clearly., • Ability to work independently as well as collaboratively across multiple departments., • High attention to detail and organizational skills in a fast-paced environment. Core Competencies • Business and financial acumen, • Analytical thinking and problem solving, • Collaboration and teamwork, • Initiative and adaptability, • Effective communication Benefits: • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.

Job Description We're currently hiring Production coordinators who will be responsible for coordinating and developing production schedules on a daily basis to meet goals. They take stock of inventory levels and facilitate providing necessary materials and components. Full time Monday - Friday $20 - $25 Apply in person at 8040 Peters Road, Suite H-100, Plantation, FL 33324 (954)397-0778 QUALIFICATIONS: • Bachelor's degree in Industrial Engineering, • 5 + years related experience in Manufacturing, • Experience in Pharmaceutical/Nutraceutical industry preferred, • Strong verbal and written communication skills, • Excellent Planning and Time Management, • Excellent computer skills, including Microsoft Office Suite and internet literate. Advanced Excel proficiency preferred, • Ability to safely and successfully perform essential job functions consistent with ADA, FMLA and other federal, state and local standards, including meeting qualitative and quantitative productivity standards., • Ability to maintain reasonably regular attendance consistent with the ADA, FMLA and other federal, state and local standards., • Creates production schedules to maximize efficiency to Picking, Pharmacy, Blending., • Compression, Encapsulation, Coating, Inspection and Packaging operations, • Performs tracking to ensure all customer orders are filled on time, • Communicates with Purchasing department to coordinate deliveries of raw materials, and packaging components., • Communicates with sales departments to update status of orders daily or as needed and required by sales., • Evaluates feedback from Research and Development and Production supervisors to create more efficiencies during production., • Coordinates with IT and VP Operations for the enhancement of the planning operations., • Coordinates with Regulatory Affairs for the re-work of returns and rejected products., • Responsible for presenting the overall plan to Management, • Allocates necessary resources for completion to process orders., • Updates and provides daily production schedule to all production supervisors, • Reviews requests of new sales orders and coordinates with Management to provide the best real time delivery dates to the Customer Service department., • Gathers information regarding problems that occur during the running of a product in order to be prepared for future scheduling., • Performs other functions as requested by the immediate Supervisor

Job Description We are seeking a bilingual (English/Spanish) Research and Development Specialist to join our growing nutraceutical company. The ideal candidate will have a strong background in product formulation, quality standards, and regulatory compliance within the nutraceutical, pharmaceutical, or food science industries. This role plays a key part in developing innovative health and wellness products, ensuring both quality and compliance. Location: Miramar, FL Schedule: Monday – Friday, 8:30 AM – 5:00 PM Salary: $28/HR Full-time Responsibilities: * Develop and reformulate nutraceutical products, including vitamins, supplements, and powders. * Conduct research to support product innovation, ingredient selection, and formulation improvements. * Perform product testing, stability studies, and documentation of results. * Ensure compliance with FDA, GMP, and industry standards. * Collaborate with Quality, Production, and Marketing teams to bring new products to market. * Maintain accurate records, technical documentation, and standard operating procedures (SOPs). * Provide bilingual communication and documentation (English/Spanish) as needed for cross-functional teams. Qualifications: * Bilingual in English and Spanish (required). * Bachelor's degree in Chemistry, Biology, Food Science, Pharmaceutical Sciences, or related field. * Experience in nutraceutical, pharmaceutical, or food manufacturing preferred. * Knowledge of GMP regulations and product development processes. * Strong analytical, problem-solving, and documentation skills. * Ability to work independently and collaboratively in a team environment.

Job Description As a Junior R&D Formulator at Sun Nutraceuticals, you will support the formulation and development of dietary supplements, with a primary focus on gummies and liquids, incorporating botanicals and functional ingredients. You will assist in creating product samples for client approval, contribute to developing appealing flavor profiles, participate in research to innovate delivery systems and optimize processes, and help with regulatory compliance. This entry-level role offers the opportunity to learn and grow in a fast-paced, collaborative environment within a small, agile team, ideal for those starting their career in nutraceutical product development. Responsibilities: • Product Formulation: Design and develop gummies, liquids, powders, and encapsulated supplements, incorporating functional ingredients to meet nutritional and sensory goals., • Flavor Development: Create and refine flavor profiles to ensure consumer appeal, masking off-notes from functional ingredients using techniques like natural flavors or cyclodextrins., • Sample Production: Prepare lab-scale product samples for client review, iterating based on feedback to ensure formulations are scalable and meet expectations., • Research & Development: Conduct R&D to innovate new product concepts, enhance ingredient delivery, and streamline manufacturing processes to reduce costs as we scale., • Regulatory Compliance: Assist with ensuring formulations comply with FDA regulations, including ingredient safety, labeling, and documentation for claims., • Process Optimization: Experiment with production techniques to improve efficiency, such as optimizing gel strength and setting time with pectin or gelatin, to support cost-effective scaling., • Education: Bachelor's degree in Food Science, Nutrition, Chemistry, Pharmaceutical Sciences, or a related field., • Experience:, • 0-2 years of experience in dietary supplement, nutraceutical, or food product development, preferably with gummies or liquids (internships or academic projects count)., • Basic exposure to formulation, flavor development, or sample creation is a plus., • Skills:, • Foundational knowledge in formulation and flavor development for dietary supplements., • Basic understanding of production processes for gummies and liquids., • Awareness of FDA regulations, cGMP, and NSF standards for dietary supplements., • Ability to assist in R&D and troubleshoot basic formulation or process challenges under supervision., • Good communication and collaboration skills for working with clients and a small team., • Preferred:, • Experience with pectin-based gummies or liquid emulsions through coursework or entry-level roles., • Familiarity with basic lab analysis techniques, such as HPLC, for raw materials and finished products., • Health Care Plan (Medical, Dental & Vision), • Paid Time Off (Vacation, Sick & Public Holidays)

Job DescriptionActalent is Hiring a Team of Analytical Scientists!!Job Description We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate documentation, and ensuring compliance with SOPs and cGMP standards. Responsibilities • Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution., • Evaluate test results and determine the acceptability of samples based on the results., • Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs., • Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards., • Review notebooks promptly and ensure compliance with SOPs., • Analyze and interpret results in both written and oral formats., • Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed., • Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.Skills & Qualifications, • Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience., • Proficiency in HPLC, UPLC, and UV-Vis techniques., • Familiarity with FDA and GMP regulations., • Ability to analyze and interpret complex data. 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 Hollywood,FL. Application Deadline This position is anticipated to close on Oct 24, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Production Coordinator – Pharmaceutical Industry Location: Miramar, FL Pay: $22.00/hour Shift: 6:00 AM – 2:00 PM (Monday to Friday) Job Summary: We are seeking a detail-oriented and bilingual Production Coordinator with experience in pharmaceutical or food manufacturing to join our team in Miramar, FL. The ideal candidate will coordinate daily production activities, ensure compliance with FDA and GMP regulations, and support overall production efficiency and quality. Key Responsibilities: * Coordinate and monitor production schedules and workflows * Ensure production goals are met while maintaining product quality standards * Communicate effectively with supervisors, operators, and quality assurance teams * Maintain accurate production records and reports * Assist in investigating and resolving production issues or deviations * Support audits and ensure ongoing compliance with FDA and GMP standards Requirements: * Minimum of 2 years of experience in pharmaceutical or food manufacturing * Bilingual (English/Spanish) – required * Strong knowledge of FDA, GMP, and safety regulations * High School Diploma or GED – required * Strong organizational and multitasking skills * Proficient in Microsoft Office (Word, Excel, Outlook) * Excellent communication and interpersonal skills * Ability to work in a fast-paced, team-oriented environment

Job DescriptionJob Summary: A leading nutraceutical/pharmaceutical manufacturer in Miramar, FL is seeking a motivated and experienced Fulfillment Manager. The ideal candidate will oversee the timely and accurate processing of orders, manage inventory levels, and ensure efficient order fulfillment, with a focus on maintaining high-quality standards. Key Responsibilities: • Oversee fulfillment operations to ensure timely and accurate order processing., • Develop and implement strategies to optimize efficiency and minimize costs while maintaining quality., • Lead, coach, and mentor a team of fulfillment associates to achieve departmental goals., • Collaborate with sales, customer service, and logistics teams to streamline processes and enhance customer satisfaction., • Monitor inventory levels and coordinate with procurement to ensure adequate stock., • Analyze data and performance metrics to identify areas for improvement and implement corrective actions.Qualifications:, • Previous experience in fulfillment or logistics, preferably in the pharmaceutical industry., • Proven leadership skills with the ability to motivate and develop a high-performing team., • Strong analytical and problem-solving abilities., • Excellent communication skills in English and Spanish (bilingual proficiency required)., • Detail-oriented with a focus on accuracy and quality.

Job Description We are seeking an experienced Manufacturing Manager to lead and oversee day-to-day operations within our nutraceutical/pharmaceutical production facility. The ideal candidate will bring proven leadership in cGMP-compliant environments and possess a strong background in managing production teams, ensuring regulatory compliance, and driving continuous improvement in quality, efficiency, and safety. Location: Miramar, FL Compensation: $30 per hour Schedule: * Standard Office Hours: 8:30 AM – 5:00 PM * Flex Shift (as needed): 10:00 AM – 7:00 PM Preferred Background: * Prior experience in nutraceutical or pharmaceutical manufacturing is highly preferred. * Strong understanding of OSHA, FDA, and cGMP regulations. * Familiarity with world-class manufacturing methods and statistical process control. Minimum Qualifications: * Bachelor's Degree (B.A. or B.S.) required. * 4–5 years of manufacturing supervisory experience in a cGMP-regulated facility. * Strong leadership and team-building skills. * Excellent verbal and written communication skills. * Proven ability to analyze production performance and implement improvements. * Working knowledge of manufacturing documentation, SOPs, and quality control practices. Key Responsibilities: * Lead and manage the manufacturing department, ensuring smooth daily operations and alignment with company goals. * Report directly to the COO while collaborating cross-functionally with QC, Sales, Operations, CEO, and CFO. * Establish and enforce production procedures to maintain high-quality standards, safety, and operational efficiency. * Ensure compliance with cGMP, SOPs, and company quality systems. * Oversee production scheduling, staffing, and shift planning—including managing overtime and additional shifts as necessary. * Monitor production runs to ensure they stay on schedule and troubleshoot any delays or issues. * Continuously evaluate and improve efficiency, machine utilization, and resource allocation. * Oversee batch record documentation, ensuring accuracy, completeness, and compliance with regulations. * Analyze finished goods (capsules and tablets) to ensure they meet specifications for potency, weight, and quality. * Provide regular training to team members on GMP practices, SOP compliance, and safety procedures. * Promote a clean, organized, and accident-free work environment by enforcing all safety protocols. * Identify areas for cost savings and implement strategies for lean manufacturing and continuous improvement. Preferred Skills & Traits: * Bilingual (English/Spanish) is a plus. * Proficient in Microsoft Office and experience with ERP systems. * Knowledge of Lean Manufacturing, Six Sigma, or similar process improvement methodologies is beneficial.

Job DescriptionFT Molecular Pathologist Job Title: Molecular Pathologist, Geriatric & Pharmacogenomics Services Location: Brooklyn, NY or Hollywood, FL Schedule: Full-Time Salary: $250,000 - $350,000 per year DOE About Infinite Medical P.C. Infinite Medical P.C. is a nationwide network of advanced practice providers and specialty clinicians committed to delivering high-quality, proactive care directly to residents in skilled nursing and long-term care facilities. Our partnership with MedElite Healthcare Management Group empowers us to focus on what matters most: providing compassionate, personalized care that meets the unique needs of each resident. Together, we champion continuous innovation and collaboration in our shared mission to redefine senior care across the country. Job Summary As the Molecular Pathologist, you will lead Infinite's molecular diagnostics and pharmacogenomics (PGx) efforts specifically tailored to residents in skilled nursing facilities (SNF), long-term care (LTC), and geriatric settings. You will be responsible for reviewing and interpreting molecular/PGx test results, integrating them into resident medication plans, working with external diagnostic labs, and helping internal clinical teams optimize treatments for an older population. Your work will support the "treat in place" model by reducing adverse drug events, minimizing hospitalizations, and improving medication‐management outcomes. Responsibilities • Review, interpret, and sign out molecular diagnostic and pharmacogenomics (PGx) reports, including germline and somatic testing relevant to older adults (e.g., drug metabolism genes, pharmacokinetic variants, etc.)., • Evaluate residents' molecular/PGx profiles to guide pharmaceutical compatibility, optimize medication regimens, reduce polypharmacy, and mitigate adverse drug reactions., • Serve as liaison to external diagnostic laboratories for referrals (sending out testing), ensuring quality, turnaround times, and appropriate assay selection., • Oversee validation and selection of molecular assays/panels relevant to LTC populations; ensure compliance with regulatory requirements (CLIA, CAP, etc.) and lab best practices., • Work collaboratively with facility medical staff, pharmacists, geriatricians, and nursing leadership to embed PGx insights into care plans., • Provide training, education, and consultative support to clinicians in SNFs/LTCs on interpreting molecular data and prescribing based on PGx., • Participate in quality assurance/performance improvement programs (QAPI), including documentation, monitoring outcomes (e.g., reduction in falls, hospitalization, ADRs), and helping facilities achieve quality metrics., • Monitor developments in molecular diagnostics, PGx guidelines (e.g., CPIC, FDA, others), and integrate evidence-based updates into MedElite's protocols., • Assist with policy, documentation, and reimbursement strategy as relevant to PGx / molecular testing in LTC settings. Requirements • MD or MD/PhD (or equivalent) with board certification or eligibility in molecular genetic pathology, genomic pathology, or comparable subspecialty., • Clinical experience interpreting molecular/PGx testing, ideally in older adult populations, or settings with high rates of polypharmacy., • Familiarity with molecular technologies (NGS panels, qPCR, variant annotation, copy number, possibly structural variation) and with bioinformatics or working with variant classification sources., • Strong clinical judgment with respect to medication safety, pharmacogenomic interaction, and resident care optimization in skilled nursing / LTC environments., • Excellent communication and collaboration skills: ability to work with facility staff (nurses, internists, pharmacists), external labs, and administrative leadership., • Experience in quality improvement/outcome monitoring, regulatory compliance in diagnostics., • Ethics, attention to detail, and ability to interpret data in the context of geriatric/older adult physiology., • Willingness to work from either Brooklyn, NY, or Hollywood, FL Benefits • Health, • Dental, • Vision, • 401K, • Paid - Subscription to Up-to-date, • Company-Sponsored Life Insurance, • Paid Time Off, • Malpractice Insurance Equal Opportunity Employer Infinite Medical P.C is an equal-opportunity employer. We acknowledge and honor the fundamental value and dignity of all individuals. We pledge ourselves to crafting and maintaining an environment that respects diverse traditions, heritages, and experiences. Infinite Medical P.C is an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based on race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. The above-noted job description is not intended to describe, in detail, the multitude of tasks that may be assigned but rather to give the applicant a general sense of the responsibilities and expectations of this position. As the nature of business demands change so, too, may the essential functions of the position. Ready to Make a Difference? Apply today and help us deliver compassionate, personalized care where it matters most.

Job Description The Regulatory Affairs Specialist oversees all regulatory matters and executes the strategy to ensure the organization complies with applicable regulations. This role involves developing processes and systems to ensure that all necessary licensing, filings, certifications, and permits are processed and monitored. The specialist establishes monitoring policies and procedures to ensure compliance with existing regulations and anticipates new or changing regulations. They coordinate with internal stakeholders to develop strategies to address changes in product, operations, or testing requirements. Additionally, the specialist investigates and addresses any reported issues of non-compliance. Duties and responsibilities: · Create and implement regulatory strategies to ensure adherence to regulations. · Preparation and submission of necessary regulatory documentation, such as licenses, certifications, 510(k) clearances, technical files, and permits. · Establish policies and procedures for continuous compliance monitoring. · Address new regulations by collaborating with internal stakeholders on strategies. · Investigate and resolve non-compliance issues. · Offer regulatory guidance to departments like product development, manufacturing, and quality assurance. · Oversees interactions with external regulatory consultants. · Act as the organization's representative in dealings with regulatory agencies and industry groups. · Functions as the Management Representative, ensuring the quality management system processes are established, implemented, and maintained. Required Qualifications: · Bachelor's degree in a related field (e.g., life sciences, engineering, regulatory affairs). · Minimum of 5-7 years of experience in regulatory affairs within the medical device, pharmaceutical, or biotechnology industries. · Strong knowledge of regulatory requirements and guidelines (e.g., FDA, EU MDR). · Excellent written and verbal communication skills. · Strong organizational and project management skills. · Ability to work effectively in a team environment and manage multiple projects simultaneously. Preferred Qualifications: · Advanced degree (e.g., Master's, PhD) in a related field. · Regulatory Affairs Certification (RAC). · Experience with international regulatory submissions and approvals. Physical / Mental Demands: · Working conditions are normal for an office environment. · Work may require weekend and evening work. · Work under stress in a fast-paced environment. · Must be alert, able to concentrate, and use good judgment. · Must be able to work under conditions that require sitting, standing, walking.

About Us Acquired by Tractor Supply Company, Allivet is a leading pet pharmacy with a dynamic presence in both retail and e-commerce. Headquartered in Miami, Florida, Allivet has one of the largest pharmacy fulfillment footprints spanning three U.S. locations. Offering a large selection of pet medications, pet health products, and veterinary supplies, the company serves pet owners, hobby farmers, and rescue organizations throughout the country. If you're driven by innovation and committed to making a positive impact on pets' lives, Allivet is the place for you. Join us in our mission to help pets live their best lives. Allivet is proud to be certified as a “Great Place to Work”, showcasing our commitment to core values and fostering an exceptional workplace environment for all employees. Purpose of the Role: The PRN Pharmacist is responsible for overseeing the dispensing of mail-order medications, providing clinical consultations, and ensuring adherence to all regulatory standards. Acting as a trusted source of pharmaceutical knowledge, the Pharmacist works to identify, resolve, and prevent medication-related issues through collaboration with veterinarians, clients, and pharmacy technicians. Key Responsibilities: • Patient Consultation: Offer guidance and counseling to patients on prescription usage, potential side effects, and drug interactions., • Clinical Oversight: Monitor medication therapies for safety and effectiveness, recommending adjustments to optimize patient outcomes., • Regulatory Compliance: Ensure all pharmacy operations align with federal, state, and local regulations, including accurate documentation and record-keeping., • Collaboration: Partner with pharmacy technicians and healthcare professionals to support patient care and improve workflow efficiency., • Continuous Education: Maintain up-to-date knowledge of pharmacy practices, new medications, and industry trends through ongoing education and training. Qualifications: • Education: Doctor of Pharmacy (Pharm.D.) degree from an accredited institution., • Licensure: Active pharmacist license in Florida; must meet all state requirements to practice., • Skills: Strong communication and interpersonal skills, with a patient-centered approach to care., • Technology: Proficiency in pharmacy management software and electronic health records (EHR). Essential Physical Demands/Work Environment: The usual and customary methods of performing the job’s functions require the following physical demands: The employee is frequently required to sit, stand, and walk for long periods of time. Why Work for Allivet? At Allivet, we're more than just a company. We are a strong community of passionate leaders dedicated to improving the lives of pets. Joining us means becoming part of a team where you can collaborate on exciting projects and truly make a difference. We offer a competitive compensation package, a comprehensive benefits package of medical, dental, vision, short-term/long-term disability, life insurance, PTO, and a 401K plan, plus company perks. Allivet is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Strong ability to troubleshoot pharmaceutical unit operations such as high shear granulation, dry granulation (slugging/roller compaction), compression, particle coating, pan/fluid bed coating, encapsulation, laser drilling, packaging, and cleaning.Ability to prepare high-quality technical documenta

Job Description We are seeking a skilled and experienced Industrial Mechanic with a strong background in electrical systems to join our pharmaceutical manufacturing team. Experience working with encapsulation machinery is highly preferred. This role is essential to maintaining production efficiency and ensuring all machinery operates safely and reliably. Location: Miramar, FL Schedule: Monday to Friday, 8:30am-5pm Hourly Rate: $22/hour Minimum Qualifications: * High School Diploma or Technical School Certification (two-year technical degree preferred) * Minimum of 5 years of experience in manufacturing and packaging environments, preferably in the pharmaceutical industry * Solid working knowledge of mechanical, electrical, pneumatic, welding, HVAC, and compressor systems * Familiarity with PLC systems and troubleshooting * Must be flexible and available to work nights and weekends if required * Ability to work well independently and collaboratively in a diverse work environment * Bilingual (English/Spanish) preferred Key Responsibilities: * Perform routine inspections, diagnostics, repairs, and maintenance on a variety of plant machinery and equipment * Troubleshoot and resolve mechanical and electrical issues, including repairs to encapsulation equipment when applicable * Conduct trial test runs and ensure machinery operates within specified parameters * Install, assemble, and test new machinery or replacement components * Adjust and calibrate machine components for optimal performance * Follow all current Good Manufacturing Practices (cGMP), safety standards, and hygiene protocols * Maintain accurate preventive and corrective maintenance records and documentation * Operate power tools and shop equipment to support repair and modification tasks * Assist with the development and implementation of preventive maintenance programs * Perform additional tasks as assigned by management This is an excellent opportunity for a reliable and knowledgeable mechanic to join a well-established company in a growing industry. If you have a strong mechanical aptitude and experience working in a regulated manufacturing environment, we encourage you to apply.

Job DescriptionDescription: JOB OVERVIEW: Physician Assistants deliver medical care alongside a physician, who oversees their work and provides medical supervision. The services that physician assistants provide may include diagnostic evaluations, therapeutic remediation, surgical assistance, and pharmaceutical prescription. ESSENTIAL FUNCTIONS INCLUDE, BUT ARE NOT LIMITED TO: • Promotes and maintains patient health by providing medical services under the supervision of a physician., • Contributes to a physician’s efficiency by identifying short-term and long-range patient care issues., • Recommends options and courses of action for patient care., • Implements physician directives., • Assesses patient health by interviewing patients and performing physical examination including obtaining, updating, and studying medical histories., • Determines abnormal conditions by administering or ordering diagnostic tests, such as X-rays and laboratory studies and interpreting test results., • Documents patient care services by charting in patient and department records., • Performs therapeutic procedures by administering injections and immunizations, suturing, and managing wounds and infections., • Instructs and counsels patients by providing normal growth and development information and providing counseling on emotional problems of daily living., • Provides community of care by developing and implementing patient-management plans., • Maintains safe and clean working environment by complying with procedures, rules, and regulations., • Protects patients and employees by adhering to infection-control policies and protocols. Complies with federal, state, and local legal and professional requirements by studying existing and new legislation; anticipating future legislation; and enforcing adherence to requirements and advising management on needed actions., • Maintains professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies. Nurse Practitioner or Physician Assistant license to practice in the State of Florida. BLS and/or ACLS required in specific areas. For Nurse Practitioners, certification by the ANCC or AANP is required and for Physician Assistants, NCCPA certification is required. EDUCATION: Physician Assistant: Must be a graduate of CAAHEP (Council on the Accreditations of Allied Health Education Programs) approved university program. NCCPA certification required. Must be licensed/certified or eligible to practice as PA in the State of Florida. Nurse Practitioner: Master's degree in Nursing required. (If licensed prior to 1998, Master's degree not required by the State of Florida.) Must have current Florida Advanced Registered Nurse Practitioner (ARNP) license or eligible to obtain Florida license. Certification by the ANCC or AANP in a specialty area required. EXPERIENCE: Minimum one year PA or APRN experience preferred but not required SKILLS: • Comfortable working in fast paced environment., • Proven work experience as a physician assistant or nurse, • Knowledge of medical guidelines and procedures regarding examination, therapy and recovery, • Familiarity with advancements in medical technology and current know-how, • Problem solving skills and ability to multi-task, • Caring and compassionate, • Excellent communication skills, both verbal and written. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential function. • Specific vision requirements include the ability to see at close range, distance vision, peripheral vision, depth perception, and the ability to adjust focus., • While performing the duties of this job, the employee is regularly required to talk and hear., • Possess the ability to fulfill any office activities normally expected in an office setting, to include, but not limited to: remaining seated for periods of time to perform computer based work, participating in filing activity, lifting and carrying office supplies (paper reams, mail, etc.), • The position walks, sits, stands, bends, lifts and moves continually during working hours., • Frequently lift and/or move over 50 pounds., • Fine hand manipulation (keyboarding)., • Travel may be required to existing or new TOI locations.

Job DescriptionActalent is Hiring a Team of ChemistJob Description We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate documentation, and ensuring compliance with SOPs and cGMP standards. Responsibilities • Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution., • Evaluate test results and determine the acceptability of samples based on the results., • Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs., • Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards., • Review notebooks promptly and ensure compliance with SOPs., • Analyze and interpret results in both written and oral formats., • Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed., • Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.Skills & Qualifications, • Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience., • Proficiency in HPLC, UPLC, and UV-Vis techniques., • Familiarity with FDA and GMP regulations., • Ability to analyze and interpret complex data. 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 Oct 20, 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 DescriptionActalent is Hiring a Team of ChemistJob Description We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate documentation, and ensuring compliance with SOPs and cGMP standards. Responsibilities • Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution., • Evaluate test results and determine the acceptability of samples based on the results., • Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs., • Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards., • Review notebooks promptly and ensure compliance with SOPs., • Analyze and interpret results in both written and oral formats., • Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed., • Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.Skills & Qualifications, • Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience., • Proficiency in HPLC, UPLC, and UV-Vis techniques., • Familiarity with FDA and GMP regulations., • Ability to analyze and interpret complex data. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Oct 20, 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 Whether you are working in a Pharmacy looking for additional income, an established healthcare sales professional, or looking to break into Medical Sales, Healthcare Marketing Group, LLC is a great opportunity for you. As a Pharmacy Relationship Manager, you will help drive the growth of our company through building and retaining customer relationships. You can even change the way healthcare is delivered to Americans. Our Pharmacy Savings Card works like GoodRx and SingleCare. With savings of up to 80% off prescriptions, we provide the highest discounts in the industry! We are now seekingPharmacy Relationship Managers in your area!* What does a Pharmacy Relationship Manager do? • Educate Pharmacy Staff about how their customers can save up to 80% on prescriptions, • Provide Savings Cards by engaging with medical offices and educating Office Staff about how their patients can save up to 80% on medications What you need to qualify: • Pharmaceutical/medical sales experience is preferred but not required, • Sales skills with a proven track record, • Exceptional interpersonal skills (building strong relationships), • Excellent verbal and written communication skills, • Ability to work independently to oversee accounts and increase revenue, • Reliable transportation (this position is partially remote and you will be visiting medical professionals in your area) *We are currently hiring Pharmacy Relationship Managers in the San Antonio metropolitan area. Please only apply to one city; your desired territories will be discussed during the interview. Benefits Training and compensation: • We include comprehensive training and ongoing coaching, • Monthly Bonuses, • Great Commission!

Job DescriptionAbout Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. • Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs, • Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Job Summary The Accounts Payable Specialist is responsible for managing the full-cycle accounts payable process, including processing vendor invoices, handling purchase orders, and ensuring timely and accurate payments. This role requires strong attention to detail, organizational skills, and the ability to collaborate with vendors and internal teams. The specialist ensures the accuracy and integrity of financial records while supporting efficient accounting operations. Key Responsibilities • Review, code, and process vendor invoices and purchase orders in accordance with company policies., • Create, maintain, and reconcile purchase orders in the ERP system., • Reconcile vendor statements and resolve discrepancies in a timely manner., • Prepare and process weekly check runs, ACH, and wire transfers., • Ensure invoices and POs have proper documentation and approvals prior to payment., • Maintain accurate vendor records, including banking information and contact details., • Respond to vendor inquiries and resolve payment issues promptly., • Assist with month-end closing activities, including AP reconciliations and accruals., • Collaborate with Procurement, Operations, and Finance teams to improve workflow efficiency., • Education: High school diploma or equivalent required; associate degree or any accounting/finance coursework a plus, but not required., • Experience: 2–4 years of hands-on accounts payable experience, including handling purchase orders., • Proficiency with ERP/accounting systems (NetSuite, SAP, Oracle, QuickBooks, or similar) and Excel., • Strong understanding of basic accounting principles and AP processes., • Excellent attention to detail, organization, and time management., • Strong communication skills and ability to interact professionally with vendors and internal teams., • Accuracy and attention to detail, • Purchase order and invoice management, • Problem-solving and analytical skills, • Vendor and stakeholder communication, • Time management and organization Benefits: • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.

Job Description We are seeking experienced Manufacturing Supervisors to oversee daily operations in a GMP-regulated nutraceutical manufacturing facility. This position plays a critical role in leading production teams, ensuring regulatory compliance, and driving operational excellence. Ideal candidates will have a strong background in nutraceutical or pharmaceutical production, along with proven leadership abilities. Location: Miramar, FL Shifts Available: * First Shift: 8:30 AM – 5:30 PM * Pay Rate: $100.000/Per Year ESSENTIAL FUNCTIONS • Oversees all aspects of the day-to-day operations of the manufacturing department., • Manages the manufacturing operations under the direction of the COO to assure quality in all aspects of the operation., • Provides day-to-day leadership to the manufacturing operators and personnel and strives to meet all quality goals., • Establishes and maintains production procedures for high manufacturing, operations, product quality, reliability, and safety standards., • Coordinates the production of manufacturing goods., • Ensures the production meets cGMP guidelines & meets SOPs., • Oversees & manages plant personnel, including scheduling overtime or extra shifts if necessary., • Monitors production run to ensure it stays on schedule and corrects any problems that may arise., • Ensures effective management of performance in the department to meet company needs., • Oversees the production process, establishing manufacturing priorities., • Determines which machines will be used., • Comes up with ways to make the production process more efficient., • Monitors product standards by ensuring the finished product meets the level of quality., • Works closely with other managers (Sales, QC, Operations, CEO, and CFO) within the company., • Ensures manufacturing personnel receive proper cGMP training, as well as safety., • Maintains a safe and organized work environment., • Verifies raw material weight check sheets to ensure that the manufacturing operation follows batching procedures and the formula accuracy of raw material weights., • Analyzes all manufactured finished goods, including capsules and tablets, to ensure they meet all specifications for potency and weights., • Reviews all manufacturing, filling, and finishing batch documentation for accuracy of information., • Assures department compliance with all safety and personal protective policies to avoid occupational accidents or injuries., • Operates within budget parameters for the department, assisting in annual departmental budget preparations., • Prepare reports on production metrics every month and annually., • Prepares employee performance evaluations, communicates meaningful feedback, and assists with the replacement/selection process, ensuring all employees receive adequate training and development., • Maintains an area network for manufacturing statistics and information., • Coaches and mentors all production employees with the intent of optimizing the productivity of the department., • Provides proper personnel training to comply with all SOPs, safety, and FDA regulations., • Conduct regular inspections and audits of production output., • Analyze production costs and identify areas for improvement., • Identify and implement process improvements to enhance efficiency and reduce waste., • Collaborate with senior management to align production goals with company objectives., • Proven track record of improving production efficiency and reducing costs. MINIMUM REQUIRED QUALIFICATIONS • Must be Bilingual English/Spanish, • Must have a Bachelor of Science Degree., • Must have at least 4 to 6 years of manufacturing supervisory skills in a CGMP environment or manufacturing facility., • Must possess strong interpersonal, written, and oral communication skills., • Must demonstrate the ability to lead and motivate others effectively., • Must have strong organizational abilities and product line analysis., • Experience with OSHA and FDA regulations is required., • Experience with statistical process control., • Experience with world-class manufacturing methods., • Proficient in manufacturing software and Microsoft Office Suite., • Knowledge of lean manufacturing and continuous improvement practices., • Ability to thrive in a fast-paced environment., • Strong leadership and team management skills., • Excellent problem-solving and analytical abilities.

Job Description Are you motivated by an unlimited earnings potential? Are you looking for a career where you can earn Bonuses, UNLIMITED Commission, with a base? Are you looking for a career opportunity? Come join our growing team! Who are we: We are a Fast 55 Award Winning, industry leading pharmaceutical distributor. We supply the generic pharmaceutical needs of Pharmacies, and Healthcare providers across the United States. We have a culture that believes we are better together. What You'll Get: • If on target with expectations, which includes Base + UNLIMITED Commission + Monthly Bonuses + Monthly Team Bonuses, First Year earnings $50,000 - $60,000, • $1000 Sign On Bonus, • Leads / Prospects given, • Career Advancement opportunities, • Paid Training + Ongoing Key Learning and Mentoring Sessions, • Flexible PTO, & Paid Holidays, • 401(k) + Company Match, • Health Care Flexible Spending Account, • Medical, Vision, Dental, • Paid Short-Term & Long-Term Disability, • Paid Life Insurance with additional purchase options, • Paid Employee Assistance Programs, • Employee Referral Bonus What You'll Need: • Persistent, enthusiastic, and assertive sales mindset, focused on developing new business and maximizing opportunities to achieve sales results., • Strong relationship building skills & a determination to achieve goals., • Motivation by UNLIMITED Commission + Bonuses., • 1+ year(s) Sales experience required., • Telesales experience a plus., • Pharmaceutical Sales experience a plus., • Excellent Interpersonal skills including communication, written and verbal used in a Telesales environment., • Associates Degree or equivalent experience preferred. What you'll be doing: • Developing new sales areas, through outbound & inbound calls, referrals, and emails to Pharmacies nationwide., • Building relationships that will increase account penetration, revenue growth and customer satisfaction., • Achieve new account acquisition, account expansion, and account retention, while facilitating Customer orders and requests., • Focusing on account retention, and strong customer management., • Executing new business opportunities on behalf of the Company., • Achieve assigned monthly sales and customer objectives, while negotiating and collaborating with customers to achieve mutually beneficial outcomes. Schedule & Location: • Monday - Friday 11:00am - 7:00pm, • Fort Lauderdale, FL KeySource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Monday - Friday 11am - 7pm