Qa Senior Specialist

Merck & Co., Inc., Rahway, NJ, USA

Base: $106,200.00 - $167,200.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Cgmp compliance
Regulatory requirements
Quality systems
Merck & Co., Inc. is seeking a Senior Quality Specialist to ensure compliance with cGMPs and regulatory requirements in manufacturing operations. The role emphasizes quality oversight, audit activities, and continuous improvement initiatives within a hybrid work environment

Job Summary

  • The Senior Quality Specialist is a key leader in ensuring site-wide compliance with cGMPs and regulatory requirements through robust quality systems and proactive auditing activities.
  • This role provides quality oversight for manufacturing operations, with primary responsibility for managing and executing critical quality systems (e.g., change control, deviation management, and document control), conducting GMP walkthroughs, and supporting internal and external inspections.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and we offer a comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Senior Quality Specialist to ensure compliance with cGMPs and regulatory requirements in manufacturing operations. The role emphasizes quality oversight, audit activities, and continuous improvement initiatives within a hybrid work environment.

Salary

Base: $106,200.00 - $167,200.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • cGMP compliance
  • regulatory requirements
  • quality systems
  • batch record review
  • SOP review

Nice-to-have

  • continuous improvement initiatives
  • team-based environment
  • leadership skills
  • proactive auditing activities

Key Requirements

  • Associate degree with five years experience
  • Bachelor's degree with three years experience
  • Familiarity with GMP documentation review
  • Understanding of cGMPs
  • US and Puerto Rico Residents Only

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter