Supervisor, Manufacturing

We are seeking an innovative and highly motivated Manufacturing Supervisor to join our team who will be responsible for ramp-up and oversight of the cGMP operations within a state-of-the-art multi-product cell therapy manufacturing facility. This individual will partner with other functions to produce cell therapy products through safe and compliant manufacturing operations according to cGMP requirements.

Requirements

• Bachelor's degree in science, engineering, or related field required
• A minimum of 6+ years of operations experience within a cGMP environment in the biotech/biopharma industry with a minimum of 3 years leadership experience
• Cell/Gene Therapy experience required, CDMO experience preferred
• Previous experience interacting directly with the FDA and other regulatory agencies
• Substantial knowledge of Quality Systems, GMP, FDA, GAMP, ISO and other applicable standards
• Demonstrated experience in managing GMP manufacturing operations and on time delivery of quality products
• Ability to execute and deliver results
• Strong analytical, problem solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability
• Excellent teamwork and interpersonal skills with ability to influence and build strong working relationships at all levels within the organization
• Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level
• Experience with Operational Excellence and/or Lean Manufacturing. Lean Six Sigma certification preferred
• Excellent organizational and communication skills
• Self-awareness integrity, authenticity, and a growth mindset

Benefits

• Competitive base salaries
• Highly subsidized Medical, Dental, and Vision Plans
• 401(k) Matching
• Free EV Charging
• Onsite lunches
• Stock options