Manager, GMP Training

Scorpion Therapeutics

Hopewell (NJ)

On-site

USD 120,000 - 170,000

Full time

14 days+
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Job summary

Scorpion Therapeutics is seeking a Manager of GMP Training for our biopharma manufacturing site in Hopewell, NJ. You will lead the site-wide GMP training program, develop curricula, and drive continuous improvement to ensure compliance and inspection readiness.

You will oversee eLearning implementation (ComplianceWire), collaborate cross-functionally, and support regulatory inspections with a focus on GMP and FDA expectations.

Qualifications

  • Bachelor's degree in Life Sciences, Quality, Education, or related field; 5+ years GMP training management.
  • Experience supporting regulatory audits and knowledge of GMP and FDA expectations.
  • On-site role at Hopewell, NJ leading site-wide GMP training program.

Responsibilities

  • Develop training curricula for GMP training program.
  • Manage eLearning system implementation and maintenance.
  • Support regulatory inspections and audits.
  • Collaborate across functions to improve training effectiveness and compliance metrics.

Skills

GMP training management
Regulatory inspections support
Cross-functional collaboration
eLearning implementation

Education

Bachelor's degree in Life Sciences, Quality, Education, or related field
Master's degree (preferred)

Tools

ComplianceWire
Veeva document systems

Job description

Role

Manager, GMP Training at a biopharma manufacturing site, responsible for leading and continuously improving the site-wide GMP training program, ensuring compliance and inspection readiness.

Responsibilities

Responsibilities include developing training curricula, managing eLMS implementation, supporting regulatory inspections, and collaborating across functions to enhance training effectiveness and compliance metrics.

Requirements

Bachelor's degree in Life Sciences, Quality, Education, or related field with 5+ years of GMP training management in regulated biotech/pharma manufacturing; experience supporting regulatory audits and a strong knowledge of GMP and FDA expectations.

Preferred qualifications

Preferred qualifications include a Master's degree and experience managing training through organizational changes.

High-Value

High-Value: GMP training, regulated manufacturing, biotech/pharma, inspection readiness, electronic Learning Management Systems (preferably ComplianceWire), Veeva document systems, and cross-functional collaboration.

Work setup

Work setup: onsite at Hopewell, NJ.

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