Cell Therapy Manufacturing Supervisor: Night Shift

Proclinical Group; Philadelphia (Philadelphia County); On-site; USD 120,000 - 125,000; Full time

Job summary

A leading life sciences recruiter is seeking a Cell Therapy Manufacturing Supervisor for the night shift in Philadelphia. The role involves overseeing aseptic manufacturing processes, ensuring compliance with safety regulations, and managing staff development. Ideal candidates will have strong leadership skills and experience in biopharmaceutical GMP operations.

Qualifications

• Experience in biopharmaceutical-based GMP manufacturing operations.
• Strong knowledge of aseptic processing in cleanroom environments.

Responsibilities

• Oversee production processes to ensure safety and compliance with cGMPs.
• Conduct performance reviews and provide feedback to management.
• Mentor and develop direct reports, fostering a culture of continuous improvement.

Skills

Aseptic Processing

Leadership

Communication

Education

Bachelor's degree in biology

Bachelor's degree in biochemistry

Bachelor's degree in bioengineering

Job description

Cell Therapy Manufacturing Supervisor - Permanent - 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 Cell Therapy Manufacturing Supervisor for the night shift. In this role, you will oversee aseptic manufacturing processes, ensuring safety and compliance with company standards.

Primary Responsibilities:

The successful candidate will play a key role in staff development, onboarding new team members, and managing deviations and CAPAs. Your expertise in cell culture and cleanroom operations will be crucial to the success of our autologous cell therapy manufacturing operations.

Skills & Requirements:

• Strong knowledge of aseptic processing in cleanroom environments.
• Ability to work in a fast-paced, team-oriented environment.
• Proactive, results-oriented with strong leadership skills.
• Excellent communication skills, both oral and written.
• Experience in biopharmaceutical-based GMP manufacturing operations.
• Bachelor's degree in biology, biochemistry, bioengineering, or related field, or equivalent experience.
• Ability to wear a half-face respirator and appropriate cleanroom attire.

The Cell Therapy Manufacturing Supervisor's responsibilities will be:

• Oversee production processes to ensure safety and compliance with cGMPs and safety regulations.
• Author and revise documentation, including SOPs, Batch Records, Deviations, and CAPAs.
• Conduct performance reviews and provide feedback to management.
• Develop and implement new practices to improve operational efficiency.
• Review batch documentation for accuracy and completeness.
• Provide oversight and ensure technicians follow proper aseptic techniques.
• Schedule and coordinate daily activities to meet production goals.
• Mentor and develop direct reports, fostering a culture of continuous improvement.
• Stay current with Good Manufacturing Practices (cGMP) guidelines.
• Build and maintain strong relationships within the team and across departments.
• Lead training, coaching, and learning initiatives.

Compensation:

• $120 000.00 - $125 000.00 Per Annum

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at [e-mail]

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.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy