Catalent Pharma Solutions Inc

Supervisor - Biomanufacturing, Central Services

Catalent Pharma Solutions Inc$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s or Associate’s degree in scientific, engineering, or biomanufacturing field, or High School Diploma with 5 years relevant experience.
  • Minimum 2 years of relevant experience preferable if degree is held.
  • GMP experience is an advantage.

Responsibilities

  • Oversee biomanufacturing operations in cleanroom environments ensuring cGMP compliance.
  • Manage and maintain manufacturing equipment, monitoring core systems functionality.
  • Author, review, and approve documents like SOPs and Batch Production Records.
  • Ensure quality compliance through documentation review and deviation investigations.
  • Lead audits and serve as liaison with clients and stakeholders for regulatory readiness.
  • Supervise and mentor a team, conducting performance management and training sessions.
  • Drive initiatives for continuous improvement and oversee change control processes.

Benefits

  • Defined career path with annual performance reviews.
  • Supportive diverse and inclusive culture.
  • Opportunities for career growth within an expanding team.
  • 152 hours of PTO plus 8 paid holidays.
  • Generous 401K match to enhance financial security.
  • Comprehensive medical, dental, and vision benefits.
  • Tuition reimbursement to aid in degree completion.
Full Job Description

Biomanufacturing Supervisor, Central Services

Position Summary:

  • Work Schedule: 10pm-8am Sunday-Wednesday
  • 100% on-site

The Manufacturing Execution – Central Services Supervisor leads a team responsible for staging, powder weighing, and solution preparation supporting upstream, downstream, and mRNA biomanufacturing operations. The role performs and oversees cGMP manufacturing activities, ensuring adherence to SOPs while maintaining compliance in a regulated environment. Responsibilities also include reviewing batch records and data, preparing technical documentation, supporting investigations and continuous improvement, and supervising 5–15 direct reports including performance management and staffing recommendations.

The Role

  • Oversee biomanufacturing operations in cleanroom environments, ensuring compliance with cGMP standards and production timelines.
  • Manage operation and maintenance of manufacturing equipment, including monitoring core systems and ensuring proper functionality.
  • Author, review, and approve documentation such as SOPs, Batch Production Records (BPRs), and related materials.
  • Ensure quality and compliance through documentation review, deviation investigations, and adherence to the Quality Management System.
  • Lead audits, serve as a liaison for clients and internal stakeholders, and support regulatory readiness.
  • Supervise staff, including training, mentoring, performance management, and leading team meetings or training sessions.
  • Oversee facility and operational upkeep, including cleanroom housekeeping, equipment maintenance, and qualification/validation activities.
  • Drive continuous improvement initiatives, training program effectiveness, and support change control and process enhancements.
  • Other duties as assigned.

The Candidate

  • Bachelor’s or Associate’s degree in a scientific, engineering, or biomanufacturing field with a minimum of 2 years of relevant experience OR
  • High School Diploma with a minimum of 5 years of relevant experience
  • GMP experience preferred
  • Physical Requirements: This position requires frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working conditions will be Heating Ventilation and Air Conditioned controlled. Ability to operate within a clean room environment as needed.

Why you should join Catalent:

  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • 152 hours of PTO + 8 paid holidays
  • Generous 401K match
  • Medical, dental and vision benefits
  • Tuition Reimbursement- Let us help you finish your degree or start a new degree!

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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