Quality Control Senior Analyst

MSD

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profile Job Location:

Cork - Ireland

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Job Description

A fantastic opportunity has arisen for a Quality Control Senior Analyst. You will be an active member of the Quality organization completing analysis/testing of samples to support the Quality release of our products.

Bring energy knowledge innovation to carry out the following:

  • Lead monitoring and analysis of pharmaceutical water systems (PW WFI Clean Steam).
  • Ensure systems meet specifications for conductivity TOC microbial count and endotoxins.
  • Oversee sampling testing and trending of water quality data.
  • Support additional activities / projects within the Quality Laboratories as required.
  • Ensure highest Quality & Compliance standards.
  • Documentation in compliance with GMP standards.
  • Coach and train new analysts in any task you are trained in.
  • Delivery of area performance to meet or exceed functional unit goals.
  • Order and manage laboratory supplies as required.
  • Support and actively seek out continuous improvements for the Quality laboratory.
  • Ensure compliance with safety health environmental and cGMP and other applicable regulations.
  • Participate in corporate and regulatory audits.
  • Participate in problem solving to get to root cause of issues.
  • Participating and supporting all Data Integrity and Technology Enabled Labs initiatives.
  • Compliance with 6S standards.

What skills you will need:

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

  • 3rd level Degree in Science or related discipline.
  • At least 5 years experience in the pharmaceutical industry or a similar operating environment which includes experience in a QC Laboratory for example a Bioassay Micro Chemistry or Raw Materials testing laboratory as applicable.
  • Demonstrated high level of scientific problem solving and facilitation skills.
  • A good knowledge of cGMP GLP Quality Systems Data Integrity and a continuous improvement mindset.
  • Knowledge of working practices required for a GMP testing laboratory.
  • Ability to set and maintain high standards of laboratory housekeeping.
  • Demonstrated ability to problem solve.
  • Ability to respond to changing priorities.
  • Demonstrated ability to fully realize improvement initiatives.
  • Ability to meet target timelines and deliver on time.
  • Demonstrated ability to drive the completion of tasks.

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the worlds 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 dont 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.

Required Skills:

Accountability Accountability Analytical Instrumentation Animal Husbandry Biological Analysis Chemical Analysis Clinical Data Interpretation Communication EHS Compliance GMP Compliance Internal Auditing Inventory Management Laboratory Safety Management Process Microbiological Analysis Personal Initiative Pharmaceutical Management Plan of Action and Milestones (POA&M) Problem Solving Qualitative Testing Quality Control Management Quality Improvement Programs Quality Management Quantitative Assay Safety Standards 5 more

Preferred Skills:

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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):

Job Posting End Date:

11/15/2025

*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

Job DescriptionA fantastic opportunity has arisen for a Quality Control Senior Analyst. You will be an active member of the Quality organization completing analysis/testing of samples to support the Quality release of our products.Bring energy knowledge innovation to carry out the following:Lead mon...
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About Company

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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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