Job Description

Are you passionate about quality control and analytical testing in the pharmaceutical industry? We are looking for a dedicated QC Bioanalytical Associate Specialist to join our dynamic team and contribute to delivering excellence in laboratory operations.

About the Role

Reporting to the QC Manager & Associate Director, you will play a key role in executing and supporting routine analytical testing using advanced techniques such as:

HPLC Analysis (IEX, SEC, RPLC)UV AnalysisCapillary ElectrophoresisVarious compendial methods on Release, In-process, Raw Materials, and Stability samples

You will also be involved in technical writing, continuous improvement projects, and supporting GMP, EHS, and audit activities to ensure our laboratory meets the highest standards.

What You’ll DoPerform and support routine analytical testing with precision and accuracyAuthor and review technical documents including deviations, protocols, reports, and proceduresParticipate in laboratory transformation and continuous improvement initiativesMaintain laboratory instruments through calibration and upkeepEnsure compliance with cGMP regulations, SOPs, and industry standardsPromote a safe, clean, and efficient laboratory environmentSupport Lean Lab and MPS standards implementationCollaborate on various QC-related projects and initiatives

What We’re Looking ForBachelor’s degree or higher in Natural Science, Chemical Engineering, or Biological Engineeringexperience in pharmaceutical laboratory testingHands-on experience with analytical testing methods and laboratory operationsFamiliarity with Six Sigma and Lean methodologiesKnowledge of GMP practices (experience in a GMP facility is a strong plus!)Strong attention to detail and commitment to data integrityExcellent communication and teamwork skills

Why Join Us?Be part of a forward-thinking company committed to innovation and qualityWork in a collaborative environment that values continuous learning and improvementOpportunity to contribute to impactful projects and grow your career in pharmaceutical QCCompetitive salary and benefits package

Ready to make a difference in pharmaceutical quality control?
Apply now and take the next step in your career with us

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Analytical Testing, Compliance Testing, GMP Compliance, Good Manufacturing Practices (GMP), High-Performance Liquid Chromatography (HPLC) Systems, Laboratory Analysis, Laboratory Testing, Quality Control Management, Quality Mindset, Raw Material Testing, Regulatory Experience, Test Lab Management

 Preferred Skills:

Job Posting End Date:

09/13/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID:R363326