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Territory: Miami North, FL - Multi-Specialty Target city for territory is Miami - will consider candidates who live within 40 miles of territory boundaries with access to a major airport. Territory boundaries include: Doral to Hollywood/Hallandale Beach and up to Pembroke Pines, Miami Beach and Hallandale Beach. SUMMARY: Are you a results-driven biopharmaceutical sales professional looking to be part of an organization that values being curious, adaptable, and accountable? Lundbeck is a global biopharmaceutical company focusing exclusively on brain health. With more than 70 years of experience in neuroscience, we are committed to improving the lives of people with neurological and psychiatric diseases. Lundbeck employees are inspired and driven by our purpose to advance brain health and transform lives. Join us on our journey of growth! We are seeking a dynamic and results-driven sales professional with a proven track record of success who is looking to grow with LundbeckOur ideal candidate will have the ability to be a specialty product expert with an understanding of requisite market complexities in order to be successful promoting our products to stakeholders in the primary care and neurology settings. As an Account Manager, you lead the promotion of our psychiatry portfolio, executing sales and marketing strategies with comprehensive clinical knowledge to drive sales performance. Our Account Managers are adept at executing against the toughest commercialization challenges in today’s rapidly changing environment and must demonstrate strong capability in the following areas: ESSENTIAL FUNCTIONS: Business Planning & Account Leadership - Ability to use digital tools and apply data-based insights to create opportunities, develop strategy & tactics, allocate resources to enhance sales execution, monitor progress and adjust direction to maximize sales performance. Selling - Deliver messages in a clear and compelling way to customers, effectively probe customer needs to handle objections, and close every call with a commitment to action to drive changes in behavior. Customer Development - Build and maintain productive internal and external relationships based on customer needs and organizational goals, incorporating “total office” account management where applicable. Local Market & Therapeutic Area Expertise - Gather and validate key trends and dynamics in the market, map account linkages, and apply comprehensive therapeutic knowledge to uncover and prioritize unique opportunities. Reimbursement - Consistently demonstrate the ability to stay informed on reimbursement dynamics, anticipate and effectively address payer access issues (IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources. Pharmaceutical Environment/Compliance - Apply knowledge of pharmaceutical and regulatory environment, including accountability and adherence to Lundbeck policies and procedures and FDA regulations regarding the promotion of pharmaceutical and medical products. REQUIRED EDUCATION, EXPERIENCE and SKILLS: • Bachelor of Arts or Bachelor of Sciences degree from an accredited college or university., • 2-5 years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience., • Must demonstrate the intellectual capacity to score highly on disease and product training exams, including being certified on product knowledge annually., • Self-starter, with a strong work ethic, tenacity, and outstanding communication skills., • Adaptability: Ability to embrace change and work collaboratively in a fast-paced team environment., • Problem-Solving: Proven analytical skills to identify solutions and overcome obstacles., • Data Analysis: Strong computer and technical skills used in analyzing data to develop both short- and long-term goals aligned with business objectives., • Must live within 40 miles of territory boundaries., • Driving is an essential duty of this job; must have a valid driver’s license with a safe driving record that meets company requirements., • Meeting and complying with reasonable industry-standard credentialing requirements of healthcare providers / customer facilities is required for continued employment with Lundbeck ., • Ability to lift, bend, push, pull and move items including, but not limited to equipment, pharmaceutical samples, and any other work-related materials up to 25 lbs. with or without reasonable accommodation. PREFERRED EDUCATION, EXPERIENCE AND SKILLS: • Recent documented successful experience selling to general practitioners (GPs) and primary care centers., • Prior experience promoting and detailing products specific to CNS/neuroscience., • Previous experience working with alliance partners (i.e., co-promotions). TRAVEL: • Willingness/Ability to travel up to 30% - 40% domestically to (a) regularly meet/interact with customer base and internal personnel within assigned territory; and (b) typically attend 4-8 internal/external conferences and meetings spanning locations within the United States. Travel must be able to be completed in a timely manner. The range displayed is a national range, and if selected for this role, may vary based on various factors such as the candidate’s geographical location, qualifications, skills, competencies, and proficiency for the role. Salary Pay Range $110,000 to $126,000 and eligibility for a sales incentive target of $39,000. Benefits for this position include flexible paid time off (PTO), health benefits to include Medical, Dental and Vision, company match 401k and company car. Additional benefits information can be found on our ___. Applications accepted on an ongoing basis. Why Lundbeck Lundbeck offers a robust and comprehensive benefits package to help employees live well and protect their health, family, and everyday life. Information regarding our benefit offering can be found on the ___. Lundbeck is committed to working with and providing reasonable accommodations to disabled veterans and other individuals with disabilities during our employment application process. If, because of a disability, you need a reasonable accommodation for any part of the application process, please visit the ___. Lundbeck is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, and any other characteristic protected by law, rule, or regulation. Lundbeck participates in ___.

Key Responsibilities • Clinical Site Operations, • Oversee day-to-day operational performance across all clinical research sites, • Ensure operational consistency across sites including workflows, staffing models, and study execution standards., • Monitor operational KPIs including enrollment, screening, visit completion, and study timelines, • Identify operational gaps and implement process improvements to enhance site performance, • Study Execution, • Ensure clinical trials are conducted in compliance with ICH-GCP, FDA regulations, and internal SOPs, • Support site readiness for newly activated studies, • Monitor study progress including enrollment milestones and protocol adherence, • Identify operational risks and implement mitigation strategies to maintain study performance, • Enrollment & Recruitment Collaboration, • Partner with patient recruitment leadership to support enrollment success across all sites, • Monitor recruitment metrics including lead flow, screening conversion, and randomization rates, • Identify operational barriers to enrollment and implement corrective strategies, • Compliance & Quality, • Support a strong culture of regulatory compliance and operational quality across all sites, • Ensure readiness for sponsor monitoring visits, audits, and regulatory inspections, • Collaborate with regulatory and quality teams to ensure adherence to SOPs and study protocols, • Operational Infrastructure, • Develop and implement standardized operational processes across the network, • Support implementation of operational dashboards and performance reporting tools, • Help establish systems that enable scalable operations across multiple clinical sites, • People Leadership, • Provide operational oversight and support to site managers and clinical research teams, • Establish performance expectations and KPIs for operational teams, • Support staff development, training, and operational best practices, • Foster a collaborative, performance-driven culture across the research network, • Site Engagement & Operational Support, • Maintain regular presence at locations to support site teams, • Work directly with site leadership to resolve operational challenges and bottlenecks, • Support sites during study start-up phases and enrollment ramp-up, • Network Growth & Expansion, • Support operational planning for new site launches and network expansion, • Assist leadership in preparing operational infrastructure for growth initiatives, • Help ensure operational readiness for new therapeutic areas and study types, • Key Internal Partnerships, • President / CEO, • Medical Director, • Regulatory & Compliance, • Study Start-Up Team, • Patient Recruitment Leadership, • Finance, • Site Managers and Clinical Staff, • Qualifications, • Bachelor’s degree in life sciences, healthcare administration, or related field, • 8+ years of clinical research experience, preferably in site operations, • 3–5 years of leadership or management experience in clinical research or healthcare operations, • Strong understanding of ICH-GCP, FDA regulations, and clinical trial site operations, • Experience working in multi-site clinical research environments preferred, • Demonstrated ability to manage operational performance and process improvement, • Strong leadership, organizational, and communication skills, • Preferred:, • Experience in CNS clinical trials or behavioral health research, • Experience with site networks or site management organizations (SMOs)

We are seeking a skilled Chemical Engineer to design, analyze, and optimize pharmaceutical manufacturing processes. The role involves leading process improvement and development projects, resolving complex technical and operational challenges, and ensuring compliance with Good Manufacturing Practices (GMP), quality standards, and regulatory requirements. The ideal candidate will have strong technical expertise, project management experience, and a continuous improvement mindset. Shift / Working Hours • Hours: 8:00 AM – 5:00 PM Mon- Fri Key Responsibilities • Analyze, design, and optimize pharmaceutical manufacturing processes (e.g., formulation, mixing, granulation, coating, sterilization), • Lead process improvement and development projects from concept through implementation, • Apply structured problem-solving methodologies (Root Cause Analysis, 5 Whys, Fishbone, FMEA) to address deviations and operational issues, • Drive process improvement initiatives focused on yield, efficiency, robustness, and scalability, • Collaborate with Production, Quality, Validation, Engineering, Maintenance, and R&D teams, • Ensure all process changes comply with GMP, regulatory requirements, and quality standards, • Develop, review, and maintain process documentation, SOPs, batch records, and technical reports, • Support process validation, revalidation, and technology transfer activities, • Analyze process data and KPIs to drive continuous improvement and risk reduction, • Lead or support CAPA investigations related to process deviations, non-conformances, and OOS results, • Participate in internal and external audits (FDA, EMA, local authorities), • Train manufacturing and technical personnel on process changes and best practices Required & Preferred Qualifications Education • Bachelor’s degree in Chemical Engineering, • 5–10 years of experience in chemical engineering, process improvement, or pharmaceutical manufacturing, • Proven experience in process development and project execution, • Strong technical problem-solving and root cause analysis skills, • Pharmaceutical manufacturing processes and unit operations, • GMP / cGMP, FDA, EMA regulations, • Process validation, scale-up, and technology transfer, • Risk management tools (FMEA, HACCP), • Statistical analysis and process capability (Cp, Cpk), • Process data analysis tools and advanced Excel Apply now

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success. At Integer, our values are embedded in everything we do. Customer We focus on our customers' success Innovation We create better solutions Collaboration We create success together Inclusion We always interact with others respectfully Candor We are open and honest with one another Integrity We do the right things and do things right Integer is a global organization providing innovative, high-quality technologies and manufacturing to Medical Device OEM's to enhance the lives of patients worldwide and high-end niche batteries for specialized applications in the energy, military, and environmental markets. We are guided by our six Values, including focus on Customers, Innovation, Collaboration, Inclusion, Candor, and Integrity. Working at Integer means you are part of a team passionately pursuing excellence in all that we do and always reaching for the next great achievement. By joining our team, you are committing, personally and professionally, to continuously improving and developing yourself and those around you as, together, we deliver for our customers. If you are a great team member and are looking to inspire others and yourself - we want you on our team! The primary purpose of this job is to lead site Environmental, Health, Safety, and Security (EHSS) initiatives to meet and exceed site and company goals. This will be achieved by leading compliance and improvement projects focused on the development and implementation of proactive EHSS systems to ensure the health and safety of all associates and visitors. As a EHSS Manager, you will have the opportunity to work in a culture of EHSS excellence driven by associate engagement. You will make an impact by: * Adhering to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. * Providing EHSS leadership by serving as the Subject Matter Expert (SME) on EHSS matters to include review, interpretation and summarization of EHSS regulations and standards to provide guidance to associates. * Serving as the EHSS leader on the Plant Leadership Team by providing EHSS input and contributions to the overall development of annual goals and objectives. * Monitoring and evaluating the impact or new laws, regulations and industry standards with a focus on seamless implementation into the site EHSS program. * Leading cross-functional teams to continuously achieve a work environment that is safe and environmentally friendly. * Ensuring records, permits, and reports are maintained and prepared according to established guidelines by local, county, state and country agencies. * Developing and implementing training for new and existing Associates on company policies, procedures and governmental regulations. * Engaging with associates at all levels and across all functions to create an inclusive environment focused on the elimination of risk and promotion of individual safety. Defining the goals and objectives for your direct reports supporting Key Performance Indicators (metrics in Safety focused on Culture, Customer and Costs) * Leading the identification of hazardous workplace conditions by conducting documented job hazard analysis and coordinates activities to ensure corrective and preventative actions are implemented. * Responding to day-to-day Associate concerns in an appropriate and timely manner * Manages the investigation of more serious work-related injuries and near miss incidents. Documents findings, root cause analysis and corrective actions. Manages workers' compensation claims and ensures timely associate return to work. * Leading the performance of EHSS reviews, measures, audits, and reports assigned by the EHSS Manager focused on attaining and maintaining compliance with EHSS laws, regulations, company policies and best practices. * Leads and trains Emergency Response Team (ERT) to be proficient in areas necessary at the facility including hazmat, incipient fire, medical or other potential emergencies. * Liaison to government agencies, emergency responders and customers * Perform other functions as required. * **TRAVEL IS 30-40% to Pembroke Pines and Palm Harbor * Leads several elements of the EHSS program by working with site associates focused on EHSS engagement goals including safety committees/teams, ergonomics, management safety audits, recurring EHSS inspections, Behavioral Based Safety (BBS), and special skills/certifications. * Promotes associate safety engagement by encouraging submittal of observations and suggestions; and reporting near-miss incidents. * Responsible for the assessment of new equipment and chemicals coming on site. * Manages EHSS internal self-assessments. * Engaged in internal and external inspections as needed to maintain compliance with EHSS requirements. The specific measures listed below may be subject to change and are not intended to be an all-inclusive list * Safety - Achievement of Integer's engagement goals of safety awareness and active involvement in supporting the implementation and sustaining of environmental, health, safety, and security initiatives. * Delivery - Achievement of scheduled tasks and milestones for assigned projects. * Productivity - Achievement of committed results, completion of assigned projects. * Cost Improvement - Cumulative incremental savings realized as a result of your accomplishments and collaboration, particularly in support of continuous improvements. * Cost Controls - Adherence to budgets as part of the EHSS team. * Engagement - Promote Associate engagement and support each associate's Individual Development Plan. * Evidence that you learn, retain, and apply knowledge. It would be great if you could share examples of accumulated technical learnings and experiences that link directly to outlined expectations of this role. Having earned a bachelor's degree in environmental, natural, or equivalent science, engineering technology, occupational safety/industrial hygiene or fire safety - is one way to demonstrate your abilities. Other ways include sharing examples of accumulated EHSS learnings and experience over a period of 5-7 years. * Professional certifications such CSP or CIH are preferred. * Ability to collaborate with other departments to meet common goals related to overall company strategy. * Certifications preferred include First Aid, CPR and AED, Laser Safety Officer, Forklift Trainer or other relevant EHSS Certifications * A calm demeanor that transcends the high energy, constantly changing production environment * Expanded knowledge of physical properties and hazards of chemicals. * Well organized with excellent recordkeeping abilities, good interpersonal skills and ability to take work direction. * PC proficiency in Microsoft Office and electronic Safety Management Systems. * A positive, can-do attitude with an underlying belief that failure is not an option Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer's success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off. U.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.

I am partnering with a clinical research site network that is seeking a PRN Principal Investigator or Sub-Investigator to support ongoing nephrology clinical trials. The role involves working directly with research participants while overseeing study activities in accordance with GCP and regulatory standards. The Clinical Research Physician Investigator or PI is responsible for administering activities to facilitate clinical research and providing clinical support for the conduct and oversight of clinical trials. • Review and hold expert knowledge of study-related activities and protocols., • Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times., • Maintain study sponsor and clinical trial confidentiality., • Performs study related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments., • Reviews and adjudicates all lab, imaging and biopsy findings., • Assists in the preparation for study monitor visits., • Performs subject screening and recruitment. Key details: • Location: Hollywood, FL (onsite), • Schedule: ~10–15 hours per week, • Role: PRN Principal Investigator or Sub-Investigator, • Patient interaction required, including physical exams and eligibility evaluations They are specifically seeking: • MD or DO, BE/BC Nephrologist in good standing and licensed in Florida, • Ability to be credentialed with Davita and Fresenius dialysis centers, • Clinical research experience required as a Sub-I or PI, • Spanish bilingual preferred

Collaborate with Supply Chain, R&D, Quality and Regulatory Affairs to qualify new suppliers and manage ongoing supplier performance. Develop and maintain supplier quality assurance programs aligned with FDA, ISO 22716 (GMP for cosmetics), and other applicable regulations. Lead investigations into su

Job DescriptionBenefits: • Competitive salary, • Health insurance, • Ensuring full ISO 13485 quality system compliance, • Optimizing manufacturing efficiency and scalability, • Overseeing supplier qualification and global sourcing (including China and Mexico), • Leading Class I, II, and III regulatory submissions, • Serve as primary operational lead with US-based contract manufacturer, • Oversee production planning, validation, and batch consistency, • Implement KPIs for quality, efficiency, and cost control, • Lead scale-up initiatives and process optimization efforts, • Ensure manufacturing documentation and traceability systems are robust and audit-readyQuality & Compliance (ISO 13485), • Maintain and improve the Quality Management System (QMS), • Develop and refine SOPs, CAPA, change control, and risk management processes (ISO 14971), • Prepare for and support regulatory audits and inspections, • Ensure adherence to FDA and international regulatory standardsRegulatory Affairs, • Lead preparation and submission of Class I, II, and III medical device registrations, • Maintain technical documentation and regulatory files, • Ensure labeling, claims, and product documentation compliance, • Support regulatory strategy for new international marketsSupplier Sourcing & Qualification, • Identify, evaluate, and qualify global suppliers for bottles, packaging, and components, • Conduct supplier audits and establish quality agreements, • 815+ years of experience in medical device or regulated skincare manufacturing, • Strong hands-on experience with ISO 13485-certified contract manufacturers, • Demonstrated experience scaling operations in a growing company environment, • Direct involvement in regulatory submissions (Class IIII preferred), • Experience managing US-based manufacturing partnershipsTechnical Competencies, • Deep knowledge of production planning and manufacturing process optimization, • Strong understanding of Quality Control systems and regulatory compliance, • Experience implementing and improving QMS frameworks, • Familiarity with pharmaceutical-grade or wound care manufacturing processesLeadership & Personal Attributes, • Proven ability to lead cross-functional initiatives, • Strong operational and strategic thinking capabilities, • Excellent problem-solving skills and attention to detail, • Ability to build systems and processes in a scaling organization, • Comfortable working in a fast-paced, high-growth environmentEducation, • Advanced degree (MBA or Engineering Masters) is a strong advantage, • ISO 13485 Lead Auditor or Regulatory certification is a plus

Job DescriptionOperations & Manufacturing Manager Lavior Pharma is seeking an experienced Operations & Manufacturing Manager to oversee manufacturing operations, supply chain management, and regulatory coordination.This role will manage contract manufacturers (CDMOs), suppliers, and production planning while ensuring manufacturing operations comply with ISO 13485 quality standards and FDA regulatory requirements.The Operations & Manufacturing Manager will play a key role in scaling Lavior’s manufacturing capabilities while maintaining regulatory compliance and operational efficiency. This position reports directly to the CEO. Key Responsibilities:Manufacturing & CDMO ManagementServe as the primary operational liaison with contract manufacturers (CDMOs).Oversee production planning, batch scheduling, and manufacturing timelines.Monitor manufacturing performance including lead time, yield, and cost efficiency.Ensure manufacturing documentation, batch records, and traceability systems are maintained and audit-ready.Support scale-up initiatives and process improvements.Supplier & Contract Manufacturer SourcingIdentify, evaluate, and onboard new contract manufacturers, CDMOs, and production partners.Source and qualify new suppliers and vendors for manufacturing components and raw materials.Manage sourcing for production materials including: • tubes, • packaging, • boxes, • printed materials, • components and labelingConduct supplier qualification and coordinate quality agreements.Perform supplier performance reviews and maintain approved supplier lists.Supply Chain & Production PlanningDevelop production forecasts and manufacturing plans aligned with company growth.Coordinate procurement and inventory planning to ensure supply availability.Manage lead times, logistics, and supplier performance.Implement systems to improve manufacturing efficiency and supply chain reliability.Cost Optimization & Pricing SupportAnalyze manufacturing costs and identify opportunities for cost optimization.Support leadership in product pricing strategy and margin improvement.Evaluate alternative suppliers and manufacturing processes to reduce costs while maintaining quality standards.Quality & ISO 13485 ComplianceSupport and maintain manufacturing operations aligned with ISO 13485 Quality Management System requirements.Ensure CDMOs and suppliers comply with quality standards and documentation requirements.Assist in implementing SOPs, CAPA processes, and quality documentation.Support preparation for quality audits and regulatory inspections.Regulatory & FDA CoordinationCoordinate testing with FDA-compliant laboratories, including:, • biocompatibility testing, • assay validation, • stability testing, • medical device product testing, • Support regulatory activities including:, • FDA 510(k) submissions, • OTC regulatory requirements, • 21 CFR Part 211 (pharmaceutical GMP), • 510(k), • OTC compliance, • 21 CFR 211 and 820EducationBachelor’s degree in one of the following:Biomedical EngineeringChemical EngineeringIndustrial EngineeringPharmaceutical SciencesSupply Chain / Operations Management Advanced degree or ISO 13485 / regulatory certification is a strong advantage. Key SkillsManufacturing process optimizationVendor negotiation and supplier qualificationRegulatory and quality complianceProduction forecasting and planningCost optimization and margin managementCross-functional leadership Why Join LaviorWork with innovative botanical-based medical technologiesHelp scale a company entering global marketsBuild and optimize manufacturing infrastructureWork directly with executive leadership to drive operational growth

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. Job Summary We are seeking a highly motivated Chemical Engineer to design, analyze, and optimize pharmaceutical manufacturing processes. The successful candidate will apply chemical engineering principles to improve process efficiency, product quality, and operational performance while ensuring full compliance with Good Manufacturing Practices (GMP), quality standards, and regulatory requirements. This role involves leading process development initiatives and resolving complex technical and operational challenges in a regulated manufacturing environment. Key Responsibilities • Analyze, design, and optimize pharmaceutical manufacturing processes, including formulation, mixing, granulation, coating, sterilization, and related unit operations., • Develop, manage, and execute process development and continuous improvement projects from concept through implementation and post-launch monitoring., • Apply structured problem-solving methodologies (e.g., Root Cause Analysis, 5 Whys, Fishbone, FMEA) to resolve process deviations and complex operational issues., • Lead process optimization initiatives focused on improving yield, efficiency, process robustness, reliability, and scalability., • Collaborate cross-functionally with Production, Quality, Validation, Engineering, Maintenance, and R&D teams to ensure seamless project execution., • Ensure all process changes and improvements comply with GMP, regulatory requirements, and internal quality standards., • Develop, review, and maintain technical documentation, including SOPs, batch records, validation protocols, and engineering reports., • Support process validation, revalidation, scale-up, and technology transfer activities., • Analyze process performance data and KPIs to identify trends, reduce variability, and mitigate operational risks., • Lead or support CAPA investigations related to process deviations, non-conformances, and out-of-specification (OOS) results., • Participate in internal and external regulatory audits and inspections (e.g., FDA, EMA, local authorities)., • Bachelor's degree in Chemical Engineering., • Minimum of 5-10 years of engineering experience in manufacturing environments, preferably within the pharmaceutical industry., • Proven experience in process development and successful project execution., • Strong background in technical problem-solving and root cause analysis., • Experience supporting process validation activities and regulatory inspections preferred., • In-depth knowledge of pharmaceutical manufacturing processes and unit operations., • Strong understanding of GMP, cGMP, and global regulatory requirements (FDA, EMA)., • Experience with process validation, scale-up, and technology transfer., • Proficiency in risk management tools such as FMEA and HACCP., • Knowledge of statistical analysis and process capability metrics (Cp, Cpk)., • Competitive salary., • Bonus program based on productivity and efficiency., • Opportunities for growth in a rapidly expanding telepharmacy practice. This is a 100% onsite role; remote or hybrid work is not available. Pay Range$85,000—$135,000 USD Benefits: • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off 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, • Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients.You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services At The Pharmacy Hub, we don't just offer jobs—we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. 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 seeking a detail-oriented Quality Control Specialist to ensure product quality, regulatory compliance, and smooth operations across our supply chain. This role works closely with vendors, purchasing, logistics, warehouse, and production teams to uphold standards and resolve issues quickly. Key Responsibilities • FSVP Program: Maintain vendor documentation and ensure FDA compliance, flagging issues to purchasing when needed., • Incoming Container QC Documentation: Track open international purchase orders, coordinate quality paperwork before arrival, and issue regular QC reports., • FDA/USDA Holds: Review release notices, update system status, and manage detained or rejected shipments to expedite resolution., • Receiving Program: Collect and inspect batch samples, complete QC and metal detector reports, and ensure accurate SAP entries for warehouse and production., • Vendor Sample Verification: Evaluate vendor samples for quality and record findings consistently., • Claims Management: Investigate customer and vendor claims, document evidence, analyze root causes, and coordinate corrective actions with stakeholders., • Documentation & Reporting: Keep accurate records, perform statistical analysis, and submit timely reports to executives., • Microbiology Oversight: Review analytical test results, assure accuracy of SOPs, assist in validation processes, and approve deviations or investigations. Operations Support: Work with colleagues to resolve quality and compliance issues, serve as backup for raw material/component release, and perform additional tasks as assigned. Qualifications • Fully bilingual: English and Spanish, • At least 2 years of experience in quality control, food safety preferred., • Experience in manufacturing and production scheduling preferred, • Strong organizational and documentation skills., • Proficiency in SAP and Excel., • Ability to collaborate across departments and with external vendors., • 75% Health care plan (medical, dental, and vision), • 5-10 Vacation Days accrued by service time, • Personal Days, • Retirement plan (401K) 3% Annual Company contribution

Job Description Bilingual Quality Assurance Internal Auditor Location: Miramar, FL Schedule: Monday to Friday, 8:30 a.m. – 5:00 p.m. Pay Rate: $20 – $25 per hour (based on experience) About the Role The Quality Assurance Internal Auditor plays a key role in ensuring that organizational processes, systems, and products comply with established quality standards and regulatory requirements. This position is responsible for conducting internal audits, identifying risks, and recommending improvements that enhance operational efficiency and product quality. The auditor works cross-functionally to promote a culture of continuous improvement, accountability, and compliance with quality management principles. Responsibilities * Plan, execute, and document internal quality assurance audits across multiple departments. * Evaluate compliance with internal policies, industry standards, and regulatory requirements. * Identify risks, non-conformances, and opportunities for process improvement, and provide actionable recommendations. * Collaborate with management and process owners to develop and monitor corrective and preventive action plans. * Prepare detailed audit reports and maintain accurate audit documentation. * Stay current with applicable quality standards, regulations, and best practices. * Support training initiatives related to quality standards and audit processes. Minimum Qualifications * Bachelor's degree in Quality Management, Engineering, Business Administration, or a related field. * Previous experience in quality assurance, internal auditing, or a similar role within a regulated industry. * Strong knowledge of quality management systems (ISO 9001 or equivalent). * Familiarity with audit methodologies, risk assessment, and corrective action processes. * Strong analytical, organizational, and communication skills. Preferred Qualifications * CIA, CQA, or similar professional certification. * Experience with FDA regulations, ISO 13485, GMP, or other industry-specific standards. * Experience using audit management software and data analysis tools. * Training in root cause analysis, Six Sigma, or Lean methodologies. * Ability to lead cross-functional audit activities and manage multiple audit projects. Skills * Strong attention to detail and analytical thinking. * Effective written and verbal communication skills. * Ability to work independently and collaboratively across departments. * Proficiency with audit tools and reporting systems.

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. Job Summary We are seeking a detail-oriented Quality Control Technician to support quality assurance and compliance activities within a non-sterile compounding pharmacy environment. This role supports day-to-day quality control functions, documentation accuracy, and regulatory compliance related to compounded preparations, controlled substances, and pharmacy operations. Key Responsibilities • Perform routine quality control checks in a non-sterile compounding environment, • Verify compounding documentation, batch records, logs, and labels for accuracy and completeness., • Assist with tracking deviations, errors, or quality issues related to compounded preparations., • Assist with CAPA activities by collecting data, maintaining logs, and confirming that corrective actions are completed, • Maintain accurate and organized quality and compliance records., • Assist with internal audits, inspections, and preparation of supporting documentation., • Work closely with pharmacists, compounding technicians, and compliance staff., • Follow and reinforce quality assurance and documentation standards., • Participate in quality, safety, and compounding-related training., • Collect and document quality data related to compounding operations and pharmacy workflows., • Assist in identifying trends or recurring issues and escalate concerns to the Quality team., • High School Diploma or GED., • 1-2 years of experience in pharmaceutical compounding., • Familiarity with USP <795>, FDA guidance, and state pharmacy regulations., • Hands-on experience with non-sterile compounding., • Florida Pharmacy Technician License is preferred, • Strong attention to detail and ability to follow written procedures, • Basic understanding of quality control principles and regulated workflows., • Hands-on experience with non-sterile compounding., • Competitive salary., • Bonus program based on productivity and efficiency., • Flexible scheduling options., • Opportunities for growth in a rapidly expanding telepharmacy practice., • Evening: 2:30 p.m. - 11:00 p.m This is a 100% onsite role; remote or hybrid work is not available. The hourly rate will vary based on experience Pay Range$20—$25 USD Benefits: • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off 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, • Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients.You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services At The Pharmacy Hub, we don't just offer jobs—we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. 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 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. Job Summary The Pharmacist is a critical role in ensuring accurate, timely, and regulatory-compliant verification of prescriptions processed during the shift. This position focuses on the second stage of prescription verification (PV2), providing a final review before fulfillment and shipment to patients. The PV2 Pharmacist must work efficiently in a high-volume production environment while maintaining exceptional attention to detail and adherence to state and federal pharmacy regulations. This role requires strong organizational skills, the ability to work independently, and a commitment to operational excellence to support the pharmacy's 24/7 fulfillment model. This position offers the flexibility to transition into a senior management roles based on the employee's performance and capabilities. Essential Functions and Responsibilities • Prescription Verification: perform PV2 verification of prescriptions to ensure accuracy, safety, and compliance with legal requirements, • Regulatory Compliance: Adhere to all federal, state, and local regulations, including DEA and FDA guidelines, while maintaining accurate records, • Quality Assurance: Identify and resolve discrepancies or issues in prescriptions to ensure medication safety and accuracy before fulfillment, • Collaboration: Work closely with pharmacy technicians, PV1 pharmacists, and fulfillment staff to ensure smooth operations during the shift, • Metrics Tracking: Monitor and maintain productivity metrics to align with pharmacy goals and efficiency benchmarks, • Operational Support: Assist in troubleshooting any issues related to prescription processing, verification systems, or workflow interruptions during the midnight shift, • Education: Doctor of Pharmacy (PharmD) or Bachelor of Pharmacy degree required, • Licensure: Must hold an active and unrestricted pharmacist license in Florida. Additional state licenses are a plus, • Proficiency in pharmacy software systems and verification tools, • Strong organizational and multitasking abilities, • Ability to work independently and make sound decisions under pressure This role operates in a fast-paced mail order pharmacy setting. It requires long periods of standing, working at computer stations, and occasionally lifting or moving items up to 25 lbs. The shift operates in a controlled environment designed to optimize productivity while ensuring regulatory compliance. Cognitive and Physical Demands • Cognitive: High attention to detail, strong problem-solving skills, and the ability to focus during extended shifts., • 9:00 p.m. - 06.00 a.m. This schedule requires flexibility to accommodate pharmacy operations and meet patient demands. Job Type: Full-time, 40 hours per week, from Monday to Friday, 100% On Site What We Offer • Competitive salary., • Up to $4000 quarterly bonus based on productivity and efficiency., • Flexible scheduling options (including evenings/weekends as needed)., • Opportunities for growth in a rapidly expanding telepharmacy practice., • Collaborative and innovative work environment focused on patient safety and compliance. Pay Range$50—$80 USD Benefits: • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off 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, • Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients.You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services At The Pharmacy Hub, we don't just offer jobs—we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. 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 DescriptionJob Summary: Validation Quality Engineer will serve as the subject matter expert (SME) and technical owner of the Master Validation Program for PML’s manufacturing facilities. This role is responsible for authoring, executing, and overseeing validation protocols, reports, and supporting documentation to ensure facilities, utilities, manufacturing processes and equipment are qualified and compliant with OTC drug and cosmetic manufacturing regulatory standards. The successful candidate will bring deep validation expertise, the ability to build and continuously improve systems, and a proven track record of technical problem-solving in cosmetic and OTC drug manufacturing operations. This individual will play a critical role in ensuring inspection readiness, regulatory compliance, and continuous improvement across validation programs. The ideal candidate will monitor systems, equipment and processes, often collaborating with process engineers, operations, or quality personnel, to assess processes and parameters against industry standards, establish validation standards, and develop performance testing and quality control measures to ensure compliance with FDA regulations and GMP standards. This hands-on leadership role combines strategic and risk-based quality system management with operational oversight to ensure product safety, efficacy, and regulatory compliance throughout equipment, systems and process lifecycles. This position requires a detail-oriented leader who can balance operational excellence with regulatory requirements in a fast-paced, client-focused manufacturing environment. Essential Duties and Responsibilities: • Develop, implement, and maintain PML’s Master Validation Program at PML’s facilities., • Lead and support commissioning, qualification, and validation (IQ/OQ/PQ) activities for facilities, utilities, manufacturing processes and equipment, • Author, review, and execute validation documentation including protocols, reports, project plans, risk assessments, CAPAs, deviations, and change controls., • Serve as SME for validation within the change control process, providing technical oversight and guidance across cross-functional teams., • Assist in management and continuous improvement of calibration programs, ensuring adherence to schedules and regulatory requirements., • Develop and report on key metrics related to areas of responsibility, including statistical analysis as needed., • Lead and/or assist in investigations and resolution of quality issues through root cause analyses and determined corrective/preventive action (CAPA) initiatives, • Assist in developing, monitoring, and acting on process data to drive continuous improvement., • Support audit and inspection readiness by presenting validation activities to regulatory authorities and customers; lead responses and corrective actions as required., • Partner with Quality, Manufacturing, Engineering, and site leadership to resolve technical issues, support process improvements, and foster a culture of compliance., • Maintain and demonstrate expertise in applicable regulatory requirements GMP, FDA regulations (21 CFR Parts 11/210/211), and ISO 22716 for cosmetics and OTC drug products., • Develop, review, write, and implement SOPs for quality validation functions., • Drive collection, analysis and trending of validation data, reports or Quality metrics, • Aids in internal audit program, as well as regulatory and customer audit inspection readiness., • Provides training for other departments as needed., • Train and mentor cross-functional teams on validation and best practices., • Bachelor’s degree in Engineering or related field., • Minimum 3 years as a validation engineer in a regulated manufacturing environment preferred (cosmetics or OTC drugs a plus)., • Extensive experience in equipment calibration and performance testing, advanced proficiency in data analysis tools and project management software, and in-depth knowledge of production processes and standards., • Exceptional analytical and problem-solving abilities, excellent leadership, communication and technical writing skills, and strong organizational abilities, • Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/ 210 / 211), including data integrity practices., • Experience working with cross-functional technology teams and enterprise systems., • Exceptional problem-solving skills, attention to detail, and the ability to manage multiple priorities in a fast-paced environment., • Strong attention to detail and organizational skills., • Effective written and verbal communication skills., • Ability to lift and move objects weighing up to 25 pounds regularly and occasionally heavier items with assistance., • Ability to stand, walk, bend, stoop, push, and pull for extended periods during shifts., • Good understanding of safety protocols and practices., • Willingness to work flexible hours, including shifts and weekends., • Ability to work in a fast-paced environment and adapt to changing priorities. At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer. Powered by JazzHR Ra26iIs5rN

Job Description Overview OnePoint Patient Care is hiring a PRN Pharmacist in Miramar, FL! Join our closed-door pharmacy team where you’ll work in a non-retail environment, dedicated to meeting the pharmaceutical needs of hospice patients. If you’re passionate about delivering exceptional service and high-quality care, we want to hear from you. Apply today and become part of a team committed to making a difference! Schedule: On-Call Benefits and perks for You! • Medical, Dental, Vision insurance, • Health Savings & Flexible Spending Accounts (up to $5,000 for childcare), • Tuition discounts & reimbursement, • 401(k), • Company Paid Time Off, • Shift Differential, • DailyPay, • Pet Insurance, • Employee wellness and discount programs *Benefits may vary by employment status Responsibilities How YOU will benefit: • Supportive team with room to work independently, • Ongoing training and career growth, • Advancement opportunities in a growing company, • Referral bonuses As a Pharmacist you will: * • Receive and evaluate prescriptions for drug appropriateness, correct dosage, potential drug interactions, and proper route of administration., • Collaborate with physicians, nurses, and other healthcare professionals to provide clinical and technical support., • Maintain up-to-date patient profiles, including medical history, and current medications (prescription and OTC)., • Provide clinical recommendations to physicians and hospice nurses regarding medication therapy changes and optimizations., • Implement and enforce policies and procedures for the safe procurement, storage, administration, and disposal of medications., • Ensure compliance with all state and federal regulatory requirements related to pharmacy practice and medication management., • Perform specialized tasks that may include:, • Working in the Controlled Drugs (Narcotics) Room., • Supervising automated machines to prepack medications., • Supervising the preparation of IV medications., • Supporting facility-based dispensing machines (e.g., Omnicell)., • Perform other pharmacy-related tasks and responsibilities as assigned. Qualifications Qualifications: Required: • Bachelor’s Degree in Pharmacy, Pharm D preferred, • License/Certification(s): current and valid pharmacist license in the state of practice, • Knowledge of drug therapy guidelines, medication safety practices, and regulatory standards (CMS, DEA, FDA)., • Proficiency in electronic medical records and pharmacy information systems, • Strong clinical judgement, and effective written and verbal communication *Position will be posted for a minimum of 7 business day

Job DescriptionLogistics Coordinator Location: Hallandale Beach, FL Employment Type: Full-Time, W-2 Job Summary We are seeking a detail-oriented Logistics Coordinator to support and coordinate day-to-day logistics activities within our medical and pharmaceutical operations. This role is responsible for executing logistics processes, tracking shipments, maintaining documentation, and coordinating with internal teams and external partners to ensure timely, compliant, and cost-effective movement of goods. Key Responsibilities * Coordinate and support inbound and outbound shipments, including domestic and international transportation, ensuring timely and accurate delivery. * Schedule pickups, deliveries, and freight movements; monitor shipment status; and resolve routine issues or delays in coordination with carriers, freight forwarders, and customs brokers. * Prepare, review, and maintain logistics and shipping documentation, including invoices, packing lists, certificates, and regulatory-required materials. * Assist with inventory tracking, lot control, expiration monitoring, and logistics recordkeeping in coordination with Operations and Finance. * Support compliance with FDA, GDP, and other applicable medical and pharmaceutical logistics requirements, escalating concerns as appropriate. * Serve as a day-to-day point of contact for logistics vendors, manufacturers, warehouses, and fulfillment partners, supporting shipment execution and issue resolution. * Track logistics costs, timelines, and service metrics; prepare reports and provide operational insights to support planning, budgeting, and decision-making. * Identify opportunities for process improvements, cost efficiencies, and service enhancements, and participate in logistics-related projects as assigned. Role Scope & Decision Authority This position is primarily execution-focused and operates within established company procedures while exercising independent judgment in routine logistics matters. The Logistics Coordinator is expected to support planning activities, vendor coordination, and operational decision-making by providing recommendations, data, and logistical insight. The scope of authority may expand over time based on experience, performance, and business needs. Qualifications * Associate’s or Bachelor’s degree in Logistics, Supply Chain, Business Administration, or a related field preferred. * 2–4 years of experience in logistics coordination, shipping, or supply chain operations. * Experience in medical, pharmaceutical, or regulated industries strongly preferred. * Familiarity with FDA, GDP, or other regulated logistics environments is a plus. * Strong organizational skills and attention to detail. * Ability to manage multiple priorities and deadlines in a fast-paced environment. * Proficiency in Excel, Google Sheets, and logistics or ERP systems. * Strong written and verbal communication skills. Benefits * Company contribution of 50% toward employee health, dental, and vision insurance premiums * Supplemental health benefits, including life insurance * Comprehensive paid time off (PTO) package * Seven (7) paid company holidays

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. About the Role We are seeking an experienced and detail-oriented Compounding Pharmacist to join our dynamic 503A compounding pharmacy team. The ideal candidate will demonstrate strong knowledge of USP <795> and <800> standards, state and federal pharmacy regulations, and best practices in non-sterile compounding. This role involves overseeing the preparation, verification, and quality assurance of compounded medications while ensuring accuracy, compliance, and patient safety. The Compounding Pharmacist will collaborate closely with compounding technicians and the Quality Control (QC) team to maintain high production standards and operational efficiency within a fast-paced pharmacy environment. Responsibilities • Review and sign off on compounding records, formulations, and batch documentation to ensure accuracy, traceability, and compliance with USP <795>/<800> and state board requirements., • Oversee and verify the accurate compounding, labeling, and dispensing of customized medications in accordance with physician prescriptions and established formulations., • Verify beyond-use dating (BUD), ingredient sourcing, calculations, and final product quality prior to dispensing., • Maintain and enforce compliance with all applicable regulations including USP, DEA, FDA, HIPAA, and state pharmacy laws., • Participate in internal audits, CAPA investigations, and quality control procedures related to compounded products., • Verify ingredient integrity, lot numbers, and certificates of analysis (COAs) before use., • Ensure all documentation, logs, and records are accurate and up to date. Doctor of Pharmacy (PharmD) or Bachelor of Science in Pharmacy from an accredited institution. * Active Florida Pharmacist License in good standing with the State Board of Pharmacy. * Minimum of 2–3 years of experience in a 503A compounding pharmacy or equivalent hands-on experience in non-sterile compounding. * Thorough understanding of USP <795>, USP <800>, DEA controlled substance regulations, and state-specific compounding requirements. * Strong attention to detail, documentation accuracy, and commitment to maintaining high quality and safety standards. * Proficient in compounding software systems and pharmacy management systems. What We Offer • Competitive salary., • Up to $4000 quarterly bonus based on productivity and efficiency., • Flexible scheduling options (including evenings/weekends as needed)., • Opportunities for growth in a rapidly expanding telepharmacy practice., • Collaborative and innovative work environment focused on patient safety and compliance. This is a full-time position, working 40 hours per week, Monday through Friday This is a 100% onsite role; remote or hybrid work is not available Pay Range$55—$80 USD Benefits: • 401(k) with up to 4% matching, • Medical, dental, vision and life insurance, • Paid time off 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, • Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients.You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services At The Pharmacy Hub, we don't just offer jobs—we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. 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 a detail-oriented and proactive Formulator Assistant to join our Product Development team. This role is ideal for someone with a background in Chemistry, Biology, Food Science, or a related field, and at least one year of experience in a regulated industry such as nutraceuticals, pharmaceuticals, or food. Location: Miramar, FL Schedule: Monday to Friday, 8:30 AM – 5:00 PM Pay Rate: $20–$25 per hour, based on experience Qualifications: * Bachelor's degree in Chemistry, Biology, Food Science, or a related field * At least 1 year of experience in a laboratory, formulation, R&D, or regulatory role within an FDA-regulated industry (nutraceuticals, pharmaceuticals, food, medical devices, personal care, etc.) * Ability to perform basic calculations (percentages, concentrations, unit conversions, pricing) * Bilingual (English and Spanish) Essential Functions: * Draft formulations for quotes, lab batches, pilots, and testing during product development * Troubleshoot formulations based on lab, pilot, testing outcomes, and pricing adjustments * Conduct basic physical and organoleptic testing (e.g., weighing, particle size measurement) * Review regulatory documentation to ensure compliance in formulation * Log and track new raw materials for assigned projects * Maintain accurate formulation records and track development progress * Write change controls and deviation documents related to formulations * Communicate project updates to the R&D Manager regularly * Participate in meetings with clients, suppliers, and cross-functional teams as needed