Specialist, Analytical Instrument Validation

Merck Merck · Pharma · NJ

The Analytical Instrument Validation Specialist will work as part of the integrated Validation and Compliance team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The role oversees and/or supports the validation of novel computerized analytical instrumentation within the GMP environment for multiple sites.

What you'd actually do

  1. Partner with scientific teams across DSCS to drive compliance and operational excellence
  2. Validate novel and time-sensitive instrumentation in GMP environments to 21CFR11 compliance
  3. Support standardization activities for System Development Life Cycle globally
  4. Support internal quality and external regulatory audits and maintain laboratory state of permanent inspection readiness within the scope of SDLC
  5. Contribute to Standard Operating Procedures (SOP) drafting

Skills

Required

  • GMP Compliance
  • GMP Environments
  • Computer System Validation (CSV)
  • Change Management
  • Standard Operating Procedure (SOP) Writing
  • Systems Development Lifecycle (SDLC)
  • Regulatory Audits
  • Regulatory Compliance
  • Analytical Instrumentation
  • Analytical Chemistry
  • Code of Federal Regulations Title 21

Nice to have

  • IT, computerized systems, software and applications
  • developing tools (e.g., Power Apps)
  • utilizing AI
  • Auditing and Compliance within pharmaceutical industry
  • Instrument commissioning, qualification, and validation (CQV)

What the JD emphasized

  • GMP environment
  • 21CFR11 compliance
  • GMP policies and procedures
  • instrument computer system validation
  • Instrument commissioning, qualification, and validation (CQV)