Specialist Quality Control (technical Resources)

Amgen UK

Hyderabad, India
On-site
Technical writing in regulated environment
Cgmp regulations knowledge
Laboratory computer systems experience
Support Amgen's global Quality Control network by providing centralized document management expertise

Job Summary

  • Support Amgen's global Quality Control network by providing centralized document management expertise.
  • Responsible for end-to-end document lifecycle management for various QC processes, including environmental monitoring and equipment management.
  • Collaborate with QC teams worldwide to ensure process harmonization, continuous improvement, and compliance with cGMP standards.

Matching Summary

Support Amgen's global Quality Control network by providing centralized document management expertise.

Skills & Requirements

Must-have

  • Technical writing in regulated environment
  • cGMP regulations knowledge
  • Laboratory computer systems experience
  • Global QC Network support

Nice-to-have

  • Innovative thinking for process transformation
  • Operational Excellence exposure
  • Drug substance/product QC understanding
  • Navigating ambiguity and problem-solving

Key Requirements

  • Microbiology and Environmental Monitoring experience
  • Quality Control laboratory experience
  • Degree in Microbiology or other Life Science
  • 12 years of related experience (High school diploma/GED)
  • 10 years of related experience (Associate’s degree)
  • 8 years of related experience (Bachelor’s degree)
  • 6 years of related experience (Master’s degree)
  • 2 years of related experience (Doctorate degree)

Work Rights

Not specified

Tailored Resume

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