Biomanufacturing Training Lead - Associate I

Catalent

Madison (WI)

On-site

USD 60,000 - 75,000

Full time

14 days+

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Benefits offered by this job

Medical, dental, vision benefits from

Job summary

Catalent’s Madison, Wisconsin site is a hi‑tech biologics development and manufacturing facility supporting research through early‑ and mid‑stage clinical production. We seek an Associate Lead I - Biomanufacturing, Training to design, deliver, and maintain training programs ensuring quality and continuous improvement.

The role is 100% onsite with a Monday–Friday 10am–6pm schedule, requiring collaboration with managers and subject matter experts to drive training effectiveness and compliance in a

Qualifications

  • Bachelor's degree in a STEM field or 4+ years of related experience.
  • Proficiency with quality systems (TrackWise, ComplianceWire) and office software.
  • Knowledge of cGMP and SOP development, training and documentation.
  • Ability to author/edit procedures and participate in CAPA investigations.

Responsibilities

  • Lead and track training programs to ensure compliance and operational excellence.
  • Design and deliver effective training materials and SOPs for manufacturing teams.
  • Collaborate with managers and SMEs to identify learning needs and evaluations.
  • Support cGMP training and audit readiness, including quality system improvements.
  • Maintain training records and provide metrics for regulatory compliance.

Skills

MS Office
TrackWise
ComplianceWire
JD Edwards
Unicorn
cGMP knowledge
SOP writing/editing
training delivery

Education

B.S./B.A. in STEM
4+ years experience in related field

Tools

TrackWise
ComplianceWire
JD Edwards
Unicorn

Job description

Catalent’s Madison, Wisconsin site is a hi‑tech biologics development and manufacturing facility supporting research through early‑ and mid‑stage clinical production. We seek an Associate Lead I - Biomanufacturing, Training to design, deliver, and maintain training programs ensuring quality and continuous improvement.

The role is 100% onsite with a Monday–Friday 10am–6pm schedule, requiring collaboration with managers and subject matter experts to drive training effectiveness and compliance in a

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