Job Title: Manufacturing TechnicianJob 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 21CFR, cGMP, and ISO13485.

ResponsibilitiesSupport 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.Essential SkillsMinimum 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.Additional Skills & QualificationsBS or MS in Biology, Chemistry, Bioengineering, or a related field.Minimum of 2 years experience working in a life science manufacturing role.Work Environment

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 & Location

This is a Contract to Hire position based out of BOCA RATON, FL.

Pay and Benefits

The pay range for this position is $25.00 - $27.00/hr.

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 BOCA RATON,FL.

Application Deadline

This position is anticipated to close on Feb 23, 2026.

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 actalentaccommodation@actalentservices.com for other accommodation options.