Job Description
Job DescriptionJob Title: Manufacturing TechnicianJob Description
As a Manufacturing Technician, you will provide essential support for manufacturing operations, including the formulation and aseptic filling of cryopreservation media, cell culture media, and supplements. You will execute and maintain documentation in compliance with applicable regulations and industry standards, such as FDA 21CFR, cGMP, and ISO13485. Additionally, you will support technical writing requirements and author various manufacturing documents.
Responsibilities
- Provide manufacturing operations support including formulation and aseptic filling of products.
- Execute and maintain documentation for manufacturing procedures, ensuring compliance with industry standards.
- Author and revise manufacturing batch records, SOPs, work instructions, and other related documents.
- Formulate, fill, and finish manufactured products in a controlled or cleanroom environment.
- Perform in-process testing of products using laboratory equipment and instrumentation.
- Monitor production processes utilizing formulas and work instructions.
- Perform experiments for development, improvement, scaling up, and optimization of manufacturing processes.
- Troubleshoot equipment and process issues, including data analysis and record keeping.
- Conduct Environmental Monitoring and cleanzone cleaning activities.
- Maintain knowledge of 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 ensure lab cleanliness.
- Support deviation investigations, change controls, and implement corrective actions.
- Assist with finished product labeling, raw material aliquoting, and re-labeling requirements.
Essential Skills
- Minimum of 2 years relevant experience in a life science manufacturing role.
- Strong attention to detail with good time management and organizational skills.
- Ability to work well under pressure and prioritize assignments in a multi-tasking environment.
- Motivated and able to work independently.
- Excellent verbal communication skills with a customer service orientation.
- Basic knowledge of Outlook, Word, Excel, and relevant software programs.
- Strong adherence to cGMPs, regulatory compliance, safety requirements, and SOPs.
Additional Skills & Qualifications
- BS or MS in Biology, Chemistry, Bioengineering, or a related field.
- Experience with aseptic techniques, cleanroom protocols, and document control.
- Familiarity with manufacturing processes, batch records, and cell culture.
Work Environment
You will work in a lab setting as part of a team, with a schedule of Monday to Friday from 9 am to 5 pm, including a 1-hour lunch break. The role offers the opportunity to contribute to leading manufacturing processes for stem cell and cell culture products, with the potential to help find cures for RNA and DNA-mediated diseases. Competitive pay is offered, with the possibility of a permanent position.
Job Type & Location
This is a Contract to Hire position based out of Coral Springs, 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 Coral Springs,FL.
Application Deadline
This position is anticipated to close on Dec 31, 2025.
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.