Inteplast Group
6100 - FS Plant Office - FMSR - SR. FORMULATOR
Inteplast Group, Miramar, Florida, United States
Job Description
Posted Thursday, August 14, 2025 at 4:00 AM | Expires Saturday, August 30, 2025 at 3:59 AM TITLE:
Sr. Formulator POSITION OBJECTIVE:
Responsible for the evaluation and development of nutraceutical formulas and formulation functions throughout the entire process of manufacturing and production, by product specification, following cGMPs and Standard Operating Procedures. QUALIFICATIONS: Ensure consistent, dependable attendance and demonstrate a willingness to accommodate non-standard work hours as necessary. Capable of effectively managing job-related stress and fostering productive workplace interactions. Requires 5 years of practical experience in nutraceutical or pharmaceutical formulation, R&D, or related functions in a nutraceutical or pharmaceutical environment. Associate or bachelor’s degree in chemistry, Chemical Engineering, Pharmaceutical Science, or other closely related disciplines. Working knowledge of pharmaceutical or nutraceutical formulation and R&D processes and techniques, including formulation, sampling, testing techniques and systems, solid dosage equipment, and dosage form development. Good knowledge of math, computer literacy, strong written and oral communication skills, high organizational skills, and attention to detail. JOB RESPONSIBILITIES: Ensure compliance with company policies and safety guidelines. Report directly to the Product Development and Regulatory Director. Communicate regularly with the President and associated Supervisor/Manager, providing detailed, up-to-date reports on current and new formulations, materials, specifications, OOS items or issues to improve current products and develop new ones. Evaluate current formulas and assist in developing new formulas for current and future products. Perform data retrieval, analysis, and reporting using Information Management Systems, Quality Management Systems, or applicable internal reporting systems. Assist in evaluating new and alternative raw materials to improve and develop products. Communicate with manufacturing, production, and packaging personnel to identify and correct quality assurance issues throughout the process. Assess equipment setup and operational issues, communicating with off-shift personnel and supervisors. Communicate effectively and professionally at all organizational levels and with external contacts. Perform formulation tasks timely and accurately. Evaluate formulas, source raw materials, and seek cost-saving alternatives. Support QC with process improvement, consistency, troubleshooting, rework, prototype development, and raw material specifications. Maintain quality standards, follow cGMPs, SOPs, MSDS specifications, Sampling and Formulation Plans, and safety policies. Report any out-of-compliance issues immediately. Contribute to the improvement of current products and development of new solid dosage nutraceutical products. Work independently or in teams to meet deadlines, pass inspections, and follow up on projects. Perform operational tasks as directed by supervisors/managers. Assist in training co-workers to fill departmental needs. Identify and help resolve process flow issues, providing feedback and solutions. MACHINES, TOOLS, EQUIPMENT, ELECTRONIC DEVICES & SOFTWARE: Proficient with MS Office Suite (Word, Excel, PowerPoint, Outlook) Florida Supplement is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.
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Posted Thursday, August 14, 2025 at 4:00 AM | Expires Saturday, August 30, 2025 at 3:59 AM TITLE:
Sr. Formulator POSITION OBJECTIVE:
Responsible for the evaluation and development of nutraceutical formulas and formulation functions throughout the entire process of manufacturing and production, by product specification, following cGMPs and Standard Operating Procedures. QUALIFICATIONS: Ensure consistent, dependable attendance and demonstrate a willingness to accommodate non-standard work hours as necessary. Capable of effectively managing job-related stress and fostering productive workplace interactions. Requires 5 years of practical experience in nutraceutical or pharmaceutical formulation, R&D, or related functions in a nutraceutical or pharmaceutical environment. Associate or bachelor’s degree in chemistry, Chemical Engineering, Pharmaceutical Science, or other closely related disciplines. Working knowledge of pharmaceutical or nutraceutical formulation and R&D processes and techniques, including formulation, sampling, testing techniques and systems, solid dosage equipment, and dosage form development. Good knowledge of math, computer literacy, strong written and oral communication skills, high organizational skills, and attention to detail. JOB RESPONSIBILITIES: Ensure compliance with company policies and safety guidelines. Report directly to the Product Development and Regulatory Director. Communicate regularly with the President and associated Supervisor/Manager, providing detailed, up-to-date reports on current and new formulations, materials, specifications, OOS items or issues to improve current products and develop new ones. Evaluate current formulas and assist in developing new formulas for current and future products. Perform data retrieval, analysis, and reporting using Information Management Systems, Quality Management Systems, or applicable internal reporting systems. Assist in evaluating new and alternative raw materials to improve and develop products. Communicate with manufacturing, production, and packaging personnel to identify and correct quality assurance issues throughout the process. Assess equipment setup and operational issues, communicating with off-shift personnel and supervisors. Communicate effectively and professionally at all organizational levels and with external contacts. Perform formulation tasks timely and accurately. Evaluate formulas, source raw materials, and seek cost-saving alternatives. Support QC with process improvement, consistency, troubleshooting, rework, prototype development, and raw material specifications. Maintain quality standards, follow cGMPs, SOPs, MSDS specifications, Sampling and Formulation Plans, and safety policies. Report any out-of-compliance issues immediately. Contribute to the improvement of current products and development of new solid dosage nutraceutical products. Work independently or in teams to meet deadlines, pass inspections, and follow up on projects. Perform operational tasks as directed by supervisors/managers. Assist in training co-workers to fill departmental needs. Identify and help resolve process flow issues, providing feedback and solutions. MACHINES, TOOLS, EQUIPMENT, ELECTRONIC DEVICES & SOFTWARE: Proficient with MS Office Suite (Word, Excel, PowerPoint, Outlook) Florida Supplement is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.
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