What are the responsibilities and job description for the Senior Cell Therapy Manufacturing Specialist position at Proclinical Staffing?
Senior Cell Therapy Manufacturing Specialist - Permanent - Philadelphia, PA
Proclinical is seeking a dedicated Senior Cell Therapy Manufacturing Specialist to join our client's team in Philadelphia.
Primary Responsibilities:
The successful candidate will focus on mastering and executing GMP cell therapy manufacturing processes, ensuring compliance with quality standards, and maintaining production schedules. This position requires a proactive approach to troubleshooting and adherence to safety protocols.
Skills & Requirements:
- Bachelor's degree required.
- Experience in biopharmaceutical GMP manufacturing operations.
- Proficiency in aseptic techniques and cleanroom activities.
- Strong technical knowledge of aseptic processing in cleanroom environments.
The Senior Cell Therapy Manufacturing Specialist's responsibilities will be:
- Develop expertise in GMP cell therapy manufacturing processes and troubleshoot as needed.
- Complete and maintain training documentation.
- Comply with quality standards and production schedules.
- Adhere to Safety SOPs, cGMP, SOPs, GDP, and OSHA regulations.
- Oversee and train operational functions such as cell counting, washing, and bioreactor operations.
- Ensure accurate mathematical calculations and aseptic techniques.
- Collect and submit samples timely and ensure record accuracy through real-time GDP review.
- Communicate equipment issues to relevant personnel.
- Perform Environmental Monitoring using electronic systems.
- Train and maintain gowning qualifications.
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
