QC Bioanalytical Senior Technician
EyeBio
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 You’ll 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 We’re Looking For
- Bachelor’s 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 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.