Manufacturing Technician
Listed on 2026-02-18
-
Manufacturing / Production
Manufacturing Engineer, Quality Engineering, Validation Engineer
Job Title:
Manufacturing Technician Job Description
Provide manufacturing operations support, including the formulation and aseptic filling of cryopreservation media, cell culture media, and cell culture supplements. Execute and maintain documentation related to manufacturing procedures, ensuring compliance with applicable regulations and industry standards such as FDA 21
CFR, cGMP, and ISO
13485.
- Support all technical writing requirements for manufacturing and operations.
- Author and revise manufacturing batch records, SOPs, work instructions, validation/qualification protocols, forms, logbooks, technical reports, CAPAs, change controls, and any other applicable documents.
- Formulate, fill, and finish manufactured products, including cryopreservation media, cell culture media, and supplements.
- Perform aseptic processes in a controlled or cleanroom environment.
- Conduct in-process testing of products using general laboratory equipment and instrumentation.
- Utilize formulas and work instructions to monitor the production process.
- Perform experiments associated with development, improvement, and scaling up or optimization of manufacturing and development processes.
- Troubleshoot issues related to equipment and process development or production, including data analysis and internal record-keeping.
- Perform Environmental Monitoring activities as required.
- Maintain current knowledge of developments in product recovery and purification processes.
- Evaluate, troubleshoot, and solve routine problems, interpreting data based on knowledge and experience.
- Perform process validation and equipment qualification as required.
- Conduct general equipment preventive maintenance and contribute to lab and equipment cleanliness.
- Support and coordinate deviation investigations and implementation of change controls or corrective and preventative actions.
- Assist with finished product labeling, raw material aliquoting, and re-labeling requirements when necessary.
- Minimum of 2 years relevant experience.
- Detail-oriented with good time management and organizational skills.
- Ability to work well under pressure and prioritize assignments in a multi-task position.
- Motivated and capable of working independently.
- Excellent verbal communication skills and customer service-oriented.
- Basic knowledge of Outlook, Word, Excel, and other software programs.
- Strong adherence to cGMPs, regulatory compliance, safety requirements, SOPs, and related documents such as SDS and manuals.
Skills & Qualifications
- BS or MS in Biology, Chemistry, Bioengineering, or a related field.
- Minimum of 2 years experience working in a life science manufacturing role.
The position is based in a lab setting as part of a team. The work schedule is Monday through Friday, from 9 am to 5 pm, with a one-hour lunch break.
Job Type & LocationThis is a Contract to Hire position based out of BOCA RATON, FL.
Pay and BenefitsThe pay range for this position is $25.00 - $27.00/hr.
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)
This is a fully onsite position in BOCA RATON, FL.
Final date to receive applicationsThis position is anticipated to close on Feb 23, 2026.
About ActalentActalent 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 actalentaccom for other accommodation options.
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