Biomanufacturing Supervisor, Central Services (Night Shift)

Catalent Pharma Solutions

Madison (WI)

On-site

USD 90,000 - 115,000

Full time

7 days ago
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Benefits offered by this job

PTO 152 hours + 8 holidays
Generous 401K match
Medical, dental and vision benefits
Tuition Reimbursement

Job summary

Catalent, Inc. in Madison, WI, seeks a Biomanufacturing Supervisor for Central Services to lead a team supporting upstream, downstream, and mRNA manufacturing. You will ensure cGMP compliance, review batch records, and manage documentation in a 10pm-8am, Sunday–Wednesday on-site schedule.

Responsibilities include supervising 5–15 staff, coordinating equipment operation, driving continuous improvement, and ensuring readiness for audits in a regulated environment.

Qualifications

  • Bachelor’s or Associate’s degree in science/engineering/biomanufacturing with ≥2 years of relevant experience, or HS diploma with ≥5 years.
  • GMP experience preferred.
  • Physical requirements: frequent sitting/standing, lifting up to 50 pounds, cleanroom environment.

Responsibilities

  • Oversee biomanufacturing operations in cleanroom environments, ensuring cGMP compliance and timelines.
  • Manage operation and maintenance of manufacturing equipment and core systems.
  • Author, review, and approve SOPs, Batch Production Records, and related materials.
  • Ensure quality through documentation review, deviation investigations, and Quality Management System adherence.
  • Lead audits, liaise with clients and internal stakeholders, support regulatory readiness.
  • Supervise staff, including training, performance management, and team meetings.

Education

Bachelor’s or Associate’s degree in scientific/engineering/biomanufacturing
High School Diploma with 5+ years relevant experience

Job description

Catalent, Inc. in Madison, WI, seeks a Biomanufacturing Supervisor for Central Services to lead a team supporting upstream, downstream, and mRNA manufacturing. You will ensure cGMP compliance, review batch records, and manage documentation in a 10pm-8am, Sunday–Wednesday on-site schedule.

Responsibilities include supervising 5–15 staff, coordinating equipment operation, driving continuous improvement, and ensuring readiness for audits in a regulated environment.

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