Job summary
Job post source
This job is directly from Merck
Job overview
The Specialist, Quality Assurance at Merck ensures compliance with GMP standards and supports quality processes across engineering, material management, and supplier quality to maintain product safety and regulatory adherence.
Responsibilities and impact
The role involves conducting supplier audits, managing CAPAs, supporting engineering and maintenance compliance, overseeing materials management, reviewing quality documentation, and contributing to internal and external audit readiness.
Compensation and benefits
The salary range is $85,600 to $134,800 with eligibility for annual bonuses and long-term incentives. Benefits include medical, dental, vision insurance, retirement plans like 401(k), paid holidays, vacation, and sick leave.
Experience and skills
Requires a Bachelor of Science in Pharmaceutical Engineering, Biotechnology, Physics, Chemistry or Biology, with 3+ years in QA roles related to engineering, material management, procurement, and audits. Knowledge of GMP regulations and proficiency in SAP and quality systems is preferred.
Career development
The position offers mentorship opportunities and involvement in quality system improvements, supporting professional growth in pharmaceutical quality assurance.
Work environment and culture
Merck promotes an inclusive environment valuing diversity, collaboration, innovation, and respect, with a hybrid work model for office-based roles in the U.S.
Company information
Merck is a global pharmaceutical company known for its commitment to quality and regulatory compliance in animal health and human pharmaceuticals.
Job location and travel
The role is U.S.-based with up to 25% travel required and follows a hybrid work schedule with three days on-site and Fridays remote for office-based employees.
Application process
Applications are accepted through Merck's official job portal with specific instructions for current employees and contingent workers; accommodations are available for applicants needing assistance.
Unique job features
This role uniquely combines quality assurance with supplier management and engineering support in a regulated pharmaceutical environment, including leadership in audits and quality system enhancements.
Company overview
Merck, also known as MSD outside the United States and Canada, is a global healthcare company that develops and manufactures a wide range of pharmaceutical products, vaccines, biologic therapies, and animal health products. The company generates revenue through the sale of prescription medicines, vaccines, and health solutions for both humans and animals. Founded in 1891, Merck has a rich history of scientific innovation and has been at the forefront of major medical advancements, including the development of the first measles vaccine.
How to land this job
Position your resume for the Specialist, Quality Assurance role at Merck by emphasizing your knowledge of GMP regulations such as FDA 21 CFR, USDA 9 CFR, ISO 9001, and ICH guidelines, alongside your experience in supplier quality management and audit execution.
Highlight your skills in supporting engineering and material management processes, including deviation investigations, change control, and qualification documentation review, as these are critical to the role.
Apply through multiple platforms including Merck’s corporate careers site and LinkedIn to maximize your chances and visibility for this position.
Connect with current employees or hiring managers within Merck’s Animal Health Quality Systems or Quality Assurance divisions on LinkedIn; ice breakers could include asking about recent audit challenges they faced or expressing interest in their approach to supplier quality improvements.
Optimize your resume for ATS by incorporating keywords such as 'GMP compliance,' 'supplier audits,' 'CAPA management,' 'change control,' and specific regulations mentioned in the job description to ensure it passes initial screenings effectively.
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