Technical Process and Manufacturing Specialist - Weston, FL
About The Position
The Technical Process and Manufacturing Specialist is responsible for the production, optimization, and quality verification of complex finished goods and specialty materials in a regulated laboratory manufacturing environment. This role supports established batch records and standard operating procedures, performs technical calculations, prepares formulations, and ensures product performance and consistency. The position involves operation and troubleshooting of analytical instrumentation, process adjustments to maintain specifications, and execution of in vitro diagnostic (IVD) manufacturing tasks. Experience with immunoassay systems, clinical analyzers, and scientific production workflows is highly desirable.
Requirements
- Execute essential duties in a regulated manufacturing environment
- Interpret technical and scientific documentation
- Write controlled documents, SOPs, reports, and protocols in prescribed formats
- Demonstrate strong attention to detail and process discipline
- Possess working knowledge of Microsoft Word, Excel, and Outlook
Nice To Haves
- Bachelor’s degree in Chemistry, Biology, Biotechnology, Biomedical Sciences, or related technical discipline preferred
- Relevant laboratory, manufacturing, or diagnostic production experience may be considered in lieu of a degree
- Associate degree combined with applicable industry experience will also be considered
Responsibilities
- Write, revise, review, and support controlled documentation related to manufacturing, process improvement, and quality activities
- Calibrate, maintain, troubleshoot, and operate scientific instruments, including: • pH meters • Spectrophotometers • Dissolved oxygen meters • Centrifuges • Clinical chemistry analyzers • Immunochemistry analyzers
- Perform technical calculations and apply statistical methods to support process control
- Work with human and animal serum, plasma, and biological materials
- Operate within a biological safety cabinet using proper aseptic technique
- Execute analytical laboratory and process manufacturing tasks supporting production, development, and optimization initiatives
- Comply with Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP) & SOPs
- Maintain accurate, compliant approved batch record documentation within controlled systems
- Collaborate cross-functionally with Manufacturing, Production, Purchasing, and QA/QC teams
- Participate in troubleshooting, process improvement, and cross-functional projects
- Maintain laboratory cleanliness and manage biohazardous and non-biohazardous waste
- Perform additional duties as required
Benefits
- Medical, dental, and vision insurance
- Company Paid Life insurance
- 401(k)
- Paid time off
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
