Catalent Pharma Solutions Inc

Supervisor, Manufacturing

Catalent Pharma Solutions Inc$110K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's in a Scientific, Engineering, or Biotech field with 4-6 years in upstream biologic production under GMP OR Bachelor's with 6-8 years OR High School Diploma/Associate with 8-10 years experience.
  • Experience in mammalian or microbial cell culture is required.
  • Solid experience with large-scale centrifuges, washers, and autoclaves.
  • Strong communication and teamwork skills for both technical and non-technical interactions.
  • Demonstrable leadership experience at Catalent may substitute external experience.

Responsibilities

  • Supervise daily manufacturing operations and personnel to ensure safe and compliant execution.
  • Lead and develop teams in GMP standards and safety procedures.
  • Foster collaboration and accountability within high-performing teams.
  • Manage performance through coaching, reviews, and retention initiatives.
  • Ensure production batches meet quality and regulatory GMP standards.
  • Authorize and maintain manufacturing documentation including SOPs and batch records.
  • Lead deviation investigations and compliance initiatives for quality improvements.

Benefits

  • Defined career path with annual performance reviews.
  • A diverse and inclusive culture.
  • Opportunities for career advancement in a life-improving organization.
  • Competitive paid time off plus 8 paid holidays.
  • Medical, dental, and vision benefits effective day one.
  • Tuition reimbursement.
Full Job Description
Job Description

Supervisor, Manufacturing

Position Summary

We have an opportunity for a Supervisor, Manufacturing to join our team. In this role, you will lead teams to execute procedures for upstream manufacturing and support areas using standard operating procedures and batch records. You will oversee production equipment operations for upstream processing, including process monitoring, media preparation, and harvesting. You will ensure all team members are fully trained and compliant before entering the production floor, while maintaining high standards of quality and safety.

Shift: Day shift 7pm-7am on a 2-2-3 rotation
Location: Harmans, MD - BWI
100% Onsite

The Role
  • Supervise day-to-day manufacturing operations, personnel, and production activities to ensure safe, efficient, and compliant execution.
  • Lead, train, coach, and develop teams in GMP requirements, safety standards, and operational excellence.
  • Build high-performing, engaged teams by fostering collaboration, accountability, diversity, and continuous development.
  • Manage employee performance through coaching, performance reviews, hiring support, onboarding, and talent retention initiatives.
  • Ensure production batches meet quality, regulatory, and GMP requirements, including batch review and closeout with Quality Assurance.
  • Author, review, and maintain manufacturing documentation, including SOPs, batch records, logbooks, validation protocols, and related records.
  • Lead deviation investigations, CAPA activities, and compliance initiatives to drive quality improvements and regulatory readiness.
  • Partner with cross-functional groups, including QA, MS&T, Engineering,
  • Facilities, Project Management, and clients, to execute production campaigns and technology transfers.
  • Oversee critical manufacturing processes, equipment operation, maintenance coordination, validation activities, and accurate scientific data analysis.
  • Drive continuous improvement initiatives by identifying process efficiencies, resolving operational challenges, and providing regular production updates to stakeholders.
  • Other duties as assigned


The Candidate
Minimum Requirements
  • Master's degree in a Scientific, Engineering, or Biotech field with 4-6 years of experience in upstream biologic production processes under Good Manufacturing Practice compliance OR
  • Bachelor's degree in a Scientific, Engineering, or Biotech field with 6-8 years of experience in upstream biologic production processes under Good Manufacturing Practice compliance OR
  • High School Diploma or Associate Degree with 8-10 years of experience in upstream biologic production processes under Good Manufacturing Practice compliance
  • Experience in mammalian or microbial cell culture is required
  • Solid experience with large-scale centrifuges, washers, and autoclaves
  • Apply scientific and technical knowledge to solve routine production challenges, operate equipment effectively, and support manufacturing operations.
  • Maintain accurate GMP documentation, including batch records, SOPs, deviations, summary reports, and related manufacturing records.
  • Demonstrate strong communication, collaboration, and teamwork skills while working effectively with both technical and non-technical stakeholders.
  • Exhibit continuous learning, adaptability, creativity, and multitasking abilities, with a commitment to professional growth and process improvement.
  • 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
  • Experience with bacterial fermentation processes in a Good Manufacturing Practice environment, including bioreactor setup and operation, aseptic processing, process monitoring, sampling, troubleshooting, and batch record documentation


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 be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work 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 lives
  • Competitive paid time off plus 8 paid holidays
  • Community engagement and green initiatives
  • Medical, dental, and vision benefits effective day one
  • Tuition reimbursement


About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Founded
2007

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