Job Description

A fantastic opportunity has arisen for a QC Bioanalytical Analyst.

This opportunity will be responsible for performing analytical testing within our Biologics laboratory. You will be key in the layout of the lab testing to ensure the process is streamlined and in line with lean methodologies.

Bring energy, knowledge, innovation to carry out the following:

• Perform and carry out a variety of routine analytical techniques including but not limited to HPLC, HIC, CE, IEX, HP-SEC, UV, Potency ELISA, PCR, pH, Colour, Osmolality, Degree of Coloration, Appearance and Raw Material testing in compliance with GMP requirements.
• Follow up-to-date practices with reference to pharmacopoeias, specifications, regulations and industry standards.
• Support the laboratory testing schedule to achieve an efficient QC system.
• Receive and manage samples that come into the lab for stability, in-process and release testing.
• Reagent preparation, cleaning, and routine equipment maintenance.
• Maintain good housekeeping and hygiene within the laboratory.
• Calibrate and maintain all designated laboratory instruments.
• Participate in risk assessments, inspections, audits, incident investigations, etc. and implement and follow-up on corrective / preventative measures.
  Ensure training is current for all job functions performed.
• Order, stock and receive laboratory supplies.
• Maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.
• Ensure that cGMP standards are maintained at all times.
• Delivery of area performance to meet or exceed performance or quality goals
• Promote and participate the implementation and maintenance of the relevant safety programmes.

What skills you will need:

In order to excel in this role, you will more than likely have:

• Degree qualification (Science/Quality/Technical).
• 1-3 years industry experience with knowledge and experience in working in a lab unit.
• Ability to work as part of a team and on own initiative in a constructive manner.
• Working knowledge of QC Systems (ELN, LIMS, LabX) and Trackwise.

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to:

Invent solutions to meet unmet healthcare needs, please apply today.

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 Chemistry, Analytical Chemistry, Assay, Biochemical Assays, Biochemical Tests, Compliance Testing, Corrective Action Management, Documentations, Enzyme Linked Immunosorbent Assay (ELISA), GMP Compliance, Good Manufacturing Practices (GMP), High-Performance Liquid Chromatography (HPLC) Systems, IS Audit, Laboratory Analysis, Laboratory Testing, Manufacturing, Microbiology Laboratory, Mycoplasma Testing, Pharmaceutical Quality Assurance, Preventive Action, Quality Control Management, Quality Improvement Programs, Quality Inspections, Quality Mindset, Raw Material Testing {+ 4 more}

Preferred Skills:

Job Posting End Date:

10/6/2025

*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.