What are the responsibilities and job description for the Senior Cell Therapy Manufacturing Associate position at Proclinical Staffing?
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.
Proclinical 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.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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Salary : $30 - $35
