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Senior Cell Therapy Manufacturing Associate
- Contract
- Analytical Chemistry
- United States
This vacancy has now expired. Please see similar roles below...
Senior Cell Therapy Manufacturing Associate - Contract - Philadelphia, PA
We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.
À±½·ÊÓÆµ is seeking a dedicated Senior Cell Therapy Manufacturing Associate to join our client's team in Philadelphia.
Primary Responsibilities:
The successful candidate will be responsible for the production of Master and Working Cell Banks and supporting the manufacture of Cell & Gene Therapy products. Your work will adhere to current Good Manufacturing Practices (cGMPs), ensuring high-quality outcomes.
Skills & Requirements:
- Degree in science or related field preferred.
- Proficiency in GMP cell therapy processes.
- Strong understanding of aseptic techniques and equipment maintenance.
- Experience with facility start-ups and technical transfers.
- Ability to analyze and interpret scientific data.
- Familiarity with regulatory compliance and cGMPs.
- Basic computer skills, including Microsoft applications.
The Senior Cell Therapy Manufacturing Associate's responsibilities will be:
- Perform and train others in aseptic techniques, ensuring compliance with best practices.
- Operate, maintain, and troubleshoot equipment, identifying needs for corrective maintenance.
- Assist in sourcing and purchasing standard equipment.
- Prepare solutions and materials, and manage material procurement activities.
- Participate in facility start-ups and technical transfer activities, providing feedback for facility fit.
- Execute and review validation activities and documentation.
- Organize materials and resolve discrepancies.
- Use support systems like LIMS proficiently, acting as a subject matter expert.
- Collect, analyze, and communicate scientific and process data.
- Ensure compliance with regulatory requirements and cGMPs, coaching others as needed.
- Author and improve Standard Operating Procedures (SOPs) and Batch Records (BRs).
- Suggest and implement continuous improvement ideas.
- Support regulatory inspections and client audits as an SME.
- Coordinate with internal groups to address manufacturing support issues.
Compensation:
$30.00 - $35.00 Per Hour
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
À±½·ÊÓÆµ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓÆµ is acting as an Employment Agency in relation to this vacancy.
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