BS Life Science Jobs at Actalent | Apply Now For The Cell Therapy Specialist Role
Are you an experienced professional in biologics manufacturing or cell therapy production? Actalent, a pioneering team in Frederick, Maryland, is seeking a Cell Therapy Specialist to join their mission of developing transformative new treatments for autoimmune diseases. This role is crucial for executing the complex manufacturing of cutting-edge cell therapy products in a Good Manufacturing Practices (GMP) environment. If you’re passionate about advancing medical science and have a keen eye for detail, this is your opportunity to contribute to safer and more potent therapies.
- Job Position: Cell Therapy Specialist
- Location: Frederick, Maryland
About the Company
Actalent is a global leader in engineering and scientific services, as well as talent solutions. The company partners with its clients to drive innovation and provide specialized expertise across a wide range of industries, including biotechnology, medical devices, and pharmaceuticals. Known for connecting top-tier professionals with leading companies, Actalent is committed to providing skilled talent and strategic solutions that help businesses achieve their goals and advance scientific and engineering breakthroughs.
Job Description
The Cell Therapy Specialist is a hands-on role focused on the complex manufacturing of cutting-edge cell therapy products. The specialist will work in a GMP (Good Manufacturing Practices) environment, executing batch records and Standard Operating Procedures (SOPs) for the production of clinical materials. The role requires strong expertise in cell culture and aseptic processing, with a strong emphasis on compliance and continuous improvement.
Key Responsibilities
- Manufacturing Execution: Execute manufacturing batch records and SOPs as part of a team to produce clinical materials.
- Documentation and Compliance: Maintain detailed, cGMP-compliant documentation, review executed records, and support internal site audits.
- Problem-Solving: Assess and resolve common manufacturing issues, document deviations and corrective and preventive actions (CAPAs), and identify root causes for process improvements.
- Training & SOPs: Undergo advanced training in cell therapy manufacturing procedures and train other team members as needed. Author and revise SOPs.
- Supply Management: Ensure all manufacturing supplies are prepared and replenished for use in the clean room. Assist management in finding alternative products and suppliers to ensure a steady supply chain.
- Collaboration: Provide expert consultation on tech transfer activities to the MSAT (Manufacturing Sciences and Technology) department.
Qualifications
- Essential Skills:
- Cell culture
- Aseptic processing
- Cell therapy or biologics manufacturing
- GMP production
- Excellent documentation skills with a focus on cGMP manufacturing.
- Additional Skills & Qualifications:
- BS Degree in Life Sciences or Engineering.
- 2+ years of experience in cGMP biologics production, with a strong preference for cell therapy experience.
- Significant knowledge of biologics manufacturing processes, cell culture, and/or cell therapy production.
- Ability to apply critical thinking and troubleshooting skills to complex manufacturing issues.
- Previous sterile gowning and aseptic processing qualifications.
- Work Environment: This is an on-site position in a cleanroom environment. The role requires the use of sterile gowning and personal protective equipment. It involves standing for extended periods (3-6 hours), the ability to lift to 30 lbs, and occasional weekend and holiday work.
- Pay Rate: $31.25 – $43.00/hr.
- Application Deadline: This position is anticipated to close on September 6, 2025.
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