Rahway, United States of America On-site

Merck & Co., Inc. is hiring an Associate Manager, Quality Control

About the Role

What You'll Do

Lead the execution and enhancement of quality control processes for veterinary vaccines, ensuring accuracy and compliance throughout production and release. Guide the adoption of testing methodologies aligned with the China Veterinary Pharmacopoeia and Veterinary GMP standards, and actively contribute to method implementation and validation.

Oversee critical laboratory activities including virus quantification, adventitious agent testing, and the management of cell and virus banks. Analyze trends in quality data to identify improvement opportunities and support initiatives to optimize lab efficiency and reduce costs.

Manage quality events such as deviations, CAPA, and change controls, leading root cause investigations and ensuring timely resolution. Prepare for and support regulatory and customer audits by compiling documentation and coordinating responses. Collaborate with R&D, Production, and other sites to resolve quality challenges, transfer methods, and conduct stability studies.

Requirements

  • Bachelor’s degree or higher in Microbiology, Biopharmaceuticals, Pharmacy, Veterinary Medicine, Biotechnology, or a related field
  • At least five years of quality control experience in the animal vaccine or biologicals industry
  • Proven familiarity with method validation, stability programs, and regulatory testing requirements
  • Hands-on expertise in cell and virus culture techniques and biological assay methods
  • Strong capability in root cause analysis, data interpretation, and technical documentation
  • Ability to lead cross-functional coordination and independently manage complex quality issues
  • Fluency in English, with strong written and verbal communication skills

Technical Expertise

Experience with analytical instrumentation, LIMS, method development, technical transfer, and forensic analysis. Proficiency in Good Manufacturing Practices, quality system management, and regulatory compliance documentation is essential.

Benefits

  • Domestic relocation support available
  • No travel required
  • Onsite work model; flexible arrangements not applicable
Required Skills
Analytical InstrumentationAnalytical Method DevelopmentGood Manufacturing Practices (GMP)Laboratory Information Management System (LIMS)Root Cause Analysis (RCA)Technical TransferTechnical WritingQuality StandardsLaboratory OperationsForensic Chemistry Analytical InstrumentationAnalytical Method DevelopmentGood Manufacturing Practices (GMP)Laboratory Information Management System (LIMS)Root Cause Analysis (RCA)Technical TransferTechnical WritingQuality StandardsLaboratory OperationsForensic Chemistry
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About company
Merck & Co., Inc.
A global pharmaceutical company engaged in the research, development, manufacturing, and marketing of prescription medicines, vaccines, biologic therapies, and animal health products.
All jobs at Merck & Co., Inc. Visit website
Job Details
Category qa_testing
Posted 13 days ago