Manufacturing Supervisor will oversee personnel and daily manufacturing activities in a cGMP Biologics manufacturing facility, ensuring compliance with cGMP and safety regulations. The supervisor will be responsible for coaching, training, and developing employees, as well as participating in cross-functional project teams.
Requirements
- Bachelor’s Degree (scientific or engineering degree preferred) and 4 or more years of experience in a GMP environment; or Associate degree (scientific or engineering degree preferred) and 6 or more years of experience in a GMP environment; or High School Diploma or GED and 8 or more years of experience in a GMP environment
- Previous supervisory experience highly preferred
- Biotech or Pharmaceutical experience preferred
- Demonstrated application of current Good Manufacturing Practices (cGMP’s) and Good Documentation Practices (GDP)
- Advanced understanding of cGMP Biotech or Pharmaceutical operations a plus
- Proficient and knowledgeable in the operation and complex troubleshooting of multiple manufacturing areas (i.e., downstream, upstream and/or media buffer)
- Has some knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management
- Advanced understanding of the scientific theory of biologics manufacturing and of biotechnology processing
- Possesses manufacturing equipment understanding, including equipment function and application
- Ability to analyze department performance and proactively identify and implement strategies to improve
- Ability to train and develop direct reports
- Must be detail-oriented and able to work in a team in a fast-paced environment
- Possess excellent written and oral communication skills
- Proficient in MS Office and related PC skills
Benefits
- 401(k) plan
- Medical, dental, vision insurance
- Short-term and long-term disability coverage
- Basic life insurance
- Tuition reimbursement program
- Paid volunteer time off
- Company holidays
- Well-being benefits