Supervisor, Fill Finish

Catalent; Baltimore (MD); On-site; USD 110,000 - 130,000; Full time

Benefits offered by this job

Career path development

Inclusive culture

Growth opportunities

Paid time off

Benefits from day one

Tuition reimbursement

Job summary

Catalent is seeking a Supervisory Fill Finish role in Baltimore, MD. You will lead GMP fill/finish manufacturing for clinical and commercial materials, ensuring safety, quality, and on-time delivery.

This on-site position reports to the Manager of Manufacturing - Fill/Finish and requires strong leadership and cross-functional coordination. The role emphasizes hands-on supervision, documentation rigor, and adherence to cGMPs, with opportunities to mentor staff and drive continuous improvement in

Qualifications

• Master’s in scientific/engineering/biotech with 4–6 years GMP manufacturing experience, including fill/finish.
• Bachelor’s in scientific/engineering/biotech with 6–8 years GMP experience, including fill/finish.
• HS or A.A. with 8–10 years GMP experience, including fill/finish.

Responsibilities

• Produce clinical and commercial material per site objectives and cGMPs.
• Serve as shift point person to assign work and coordinate emergencies.
• Maintain accurate batch records and SOPs; ensure updated documentation.
• Oversee safe, compliant, and quality-focused manufacturing operations.
• Lead safety training and cross-training for staff; drive continuous improvement.
• Review regulations and industry guidance; initiate non-conformances and investigations.

Skills

GMP Fill/Finish

Leadership

Cross-functional coordination

Documentation & compliance

Problem solving

Onsite presence

Process improvement

Education

Master's degree in scientific/engineering/biotech

Bachelor's degree in scientific/engineering/biotech

High school/Associate degree with GMP experience

Job description

About Site

Our Gene Therapy facility, located at the University of Maryland (UMD) BioPark in the city of Baltimore, MD, specializes in upstream and downstream process development of viral vectors for clinical applications. Baltimore is a hub of national and international travel and communications and is also home to and near major universities and several federal agencies, including the FDA, USDA, NIH, Johns Hopkins University, and UMD Schools of Medicine. The facility houses process development labs and CGMP cleanroom suites for Phase 1 and 2 programs focused on a variety of transformative technologies, including AAV and other viral vectors, vaccines, and oncolytic immunotherapies.

Supervisor, Fill Finish Role

Position Summary

We have an opportunity for a Supervisor, Fill Finish to join our team supporting GMP Fill Finish manufacturing processes. This role applies broad knowledge of theories, techniques, and principles to solve operational and routine tasks in the aseptic production of finished drug product biologics for Phase I/II and commercial GMP manufacturing. The Supervisor plays a key role in ensuring patient safety by manufacturing life‑saving medicines right the first time. Quality, safety, and on‑time delivery are essential to success in this position. The Supervisor Fill/Finish reports to the Manager, Manufacturing - Fill/Finish.

Shift

2nd shift, Monday - Friday, 2pm-10:30pm.

Location

Baltimore, MD - BioPark

Work Arrangements

100% Onsite

Job Description / Responsibilities

• Produce clinical and commercial material annually that meets site objectives and complies with cGMPs and safety regulations.
• Serve as the point person on shift to assign and distribute work and coordinate emergency situations.
• Ensure documentation, including batch records and standard operating procedures, is accurate and updated as required.
• Oversee safe, environmentally responsible, and quality‑compliant manufacturing operations.
• Facilitate GMP and safety training for staff, focusing on cross‑training and continuous improvement.
• Recommend equipment and supply purchases within production areas.
• Exhibit safety leadership by example, using proper personal protective equipment when performing job functions.
• Demonstrate understanding of operations performed in the production unit.
• Manage shift schedules and summarize progress at the end of each shift.
• Lead and mentor staff, conduct performance reviews, set annual goals, and hold one‑on‑one meetings.
• Communicate departmental results effectively through team discussions and documentation.
• Ensure cGMP compliance in all documentation, reports, and records.
• Initiate non‑conformances and complete investigations to support timely closure of deviations.
• Review current regulations, industry guidance, and other applicable professional documentation.
• Perform other duties as assigned.

The Candidate

Minimum Requirements

• Master’s degree in a Scientific, Engineering, or Biotech field with 4–6 years of biopharmaceutical GMP manufacturing experience, including fill/finish processes and understanding of the drug development lifecycle; OR
• Bachelor’s degree in a Scientific, Engineering, or Biotech field with 6–8 years of biopharmaceutical GMP manufacturing experience, including fill/finish processes and understanding of the drug development lifecycle; OR
• High school diploma or associate degree with 8–10 years of biopharmaceutical GMP manufacturing experience, including fill/finish processes and understanding of the drug development lifecycle.
• Strong experience in GMP fill/finish manufacturing operations with a solid understanding of the drug development process.
• Extensive knowledge of fill/finish manufacturing, including aseptic hand filling and automated liquid vial filling.
• Proven ability to coordinate cross‑functional manufacturing activities to meet production schedules and objectives.
• Demonstrated leadership skills, with the ability to deliver results in a fast‑paced environment while motivating, mentoring, and developing teams.
• Strong troubleshooting and problem‑solving capabilities grounded in scientific and engineering principles, with a focus on continuous improvement.
• Excellent verbal and written communication skills; position requires full onsite presence with no remote or hybrid work option.
• Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

Preferred Skills & Background

• Proven track record of leading or supervising hands‑on cGMP manufacturing operations.

Pay

The anticipated salary range for this position in MD is $110,000 – $130,000 plus bonus. The final salary offered to a successful candidate may vary and will depend on factors such as experience, skillset, education, and business needs. Catalent is a multi‑state employer, and this range may not reflect positions in other states.

Why You Should Join Catalent

• Defined career path with annual performance reviews and feedback.
• Diverse and inclusive culture.
• Opportunities for career growth within an organization dedicated to improving and saving lives.
• Competitive paid time off plus 8 paid holidays.
• Community engagement and green initiatives.
• Medical, dental, and vision benefits effective on the first day of employment.
• Tuition reimbursement program.

Equal Opportunity Employer

Catalent is an Equal Opportunity Employer, including disability and veterans.

Accommodation

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Volunteer Work Disclosure

Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

Massachusetts Lie Detector Test Notice

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.