QC Bioanalytical Senior Technician
QC Bioanalytical Senior Technician
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Job Description
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 Analysis
- Capillary Electrophoresis
- Various 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 Youll Do
- Perform and support routine analytical testing with precision and accuracy
- Author and review technical documents including deviations protocols reports and procedures
- Participate in laboratory transformation and continuous improvement initiatives
- Maintain laboratory instruments through calibration and upkeep
- Ensure compliance with cGMP regulations SOPs and industry standards
- Promote a safe clean and efficient laboratory environment
- Support Lean Lab and MPS standards implementation
- Collaborate on various QC-related projects and initiatives
What Were Looking For
- Bachelors degree or higher in Natural Science Chemical Engineering or Biological Engineering
- experience in pharmaceutical laboratory testing
- Hands-on experience with analytical testing methods and laboratory operations
- Familiarity with Six Sigma and Lean methodologies
- Knowledge of GMP practices (experience in a GMP facility is a strong plus!)
- Strong attention to detail and commitment to data integrity
- Excellent communication and teamwork skills
Why Join Us
- Be part of a forward-thinking company committed to innovation and quality
- Work in a collaborative environment that values continuous learning and improvement
- Opportunity to contribute to impactful projects and grow your career in pharmaceutical QC
- Competitive 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:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
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 ManagementPreferred Skills:
Job Posting End Date:
09/13/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Senior IC
Employment Type
Full-Time
