Spclst, Research

Merck & Co., Inc.

West Point, Pennsylvania, United States
Base: $96,200.00 - $151,400.00; bonus/equity: annu...
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Bachelor's degree in analytical chemistry
3+ years post-degree industry experience
Experience working within a gmp environment
** Merck & Co., Inc. is seeking a Metrology and Validation Specialist for their Pharmaceutical Analysis & Digital Technologies department at their West Point, Pennsylvania facility. The ideal candidate will have a background in analytical chemistry, experience in a GMP environment, and strong communication skills to collaborate effectively across teams while ensuring compliance and operational excellence. **

Job Summary

  • The role oversees and supports the onboarding, qualification, validation, and routine maintenance of analytical equipment and instrumentation within a GMP environment.
  • The successful candidate will join scientific and technical problem solvers dedicated to creating life-changing medicines while collaborating in a fast-paced, integrated, multidisciplinary team environment.
  • Employees are eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

Match Score: 75

** Merck & Co., Inc. is seeking a Metrology and Validation Specialist for their Pharmaceutical Analysis & Digital Technologies department at their West Point, Pennsylvania facility. The ideal candidate will have a background in analytical chemistry, experience in a GMP environment, and strong communication skills to collaborate effectively across teams while ensuring compliance and operational excellence. **

Salary

Base: $96,200.00 - $151,400.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • Bachelor's degree in analytical chemistry
  • 3+ years post-degree industry experience
  • Experience working within a GMP environment
  • Understanding of GMP policies and procedures
  • Computer system validation compliance with 21CFR11

Nice-to-have

  • Experience leading a team for a common goal
  • Demonstrated commitment to inclusion
  • Experience developing tools like Power Apps or utilizing AI
  • Experience supporting internal and external quality audits
  • Strong technical and innovative problem solving skills

Key Requirements

  • Bachelor's degree in analytical chemistry or related field
  • 3+ years relevant industry experience post-degree
  • Proven track record in GMP environments
  • Knowledge of 21CFR11 compliance requirements

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter