Associate Specialist, Quality Control

Merck & Co., Inc., commonly known as Merck Sharp & Dohme LLC, is a global pharmaceutical leader headquartered in Rahway, New Jersey. With a rich legacy of innovation and commitment to improving health worldwide, Merck focuses on the discovery, development, and manufacture of a wide range of medicines, vaccines, and animal health products. The company is renowned for its dedication to quality, scientific excellence, and compliance with all regulatory standards, offering a comprehensive portfolio that serves millions of patients and customers globally. It prides itself on fostering an inclusive and collaborative environment that values diversity, integrity, and continuous improvement. Merck is dedicated to attracting and retaining talented professionals who are passionate about advancing medical science and delivering high-quality healthcare solutions.

The Associate Specialist, Quality Control role at Merck plays a critical part in ensuring the integrity and safety of the company's pharmaceutical products. This position focuses on performing microbiological, chemical, and analytical testing and sampling to uphold Merck's stringent quality standards and regulatory compliance. Partnering closely with various internal departments such as Production, Quality Assurance, Validation, Facilities, and external manufacturing sites, the Associate Specialist is integral in supporting Merck's global commitment to delivering safe, effective medicines on time to customers and patients worldwide.

In this role, you will conduct a wide range of tests including sterility testing, moisture detection, cell dry weight assessments, and environmental monitoring activities like active air and surface sampling. Your work aids in the release testing of finished products and ongoing in-process tests to maintain continuous product quality. You will also analyze data, troubleshoot process issues, and contribute to continuous improvement initiatives. Your communication skills will support informational exchanges and collaboration across departments, ensuring that quality control processes align seamlessly with business objectives.

This position requires a bachelor's degree in Biology, Microbiology, Biochemistry, or a related field, along with at least one year of relevant experience in the pharmaceutical or a similar industry. You will be expected to have proficiency in aseptic technique, environmental and water system monitoring, and understanding of Good Laboratory Practices and current Good Manufacturing Practices (cGMPs). Familiarity with laboratory software systems such as LIMS and SAP is beneficial. Merck values adaptability, teamwork, analytical skills, and a proactive approach to solving technical and operational challenges.

The role is full-time regular employee status, working 1st shift days with weekends required (Sunday-Thursday or Tuesday-Saturday). The position does not involve relocation or visa sponsorship and includes about 10% travel. While hazardous materials may be handled, no driving license is required. Merck offers a competitive salary range of $65,100 to $102,500 annually, commensurate with experience and qualifications, alongside annual bonuses and potential long-term incentives.

Merck provides an extensive benefits package including medical, dental, vision insurance, retirement plans like 401(k), paid holidays, vacation, compassionate leave, and sick days. The company is an Equal Employment Opportunity Employer that embraces diversity and inclusion and welcomes applicants with various backgrounds and experiences. If you are passionate about quality control in pharmaceuticals and want to be part of a globally respected organization, this role offers an excellent opportunity to contribute meaningfully to healthcare advancements.