QC Analyst (Drug Product)

Regeneron Pharmaceuticals, Inc

Munster

On-site

EUR 25,000 - 40,000

Full time

14 days+
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Job summary

Regeneron Pharmaceuticals, Inc. in Ireland (Raheen, Limerick) is seeking a QC Analyst (Drug Product) to join our QC Chemistry, Drug Product Testing team. This role tests according to approved procedures to support release and stability programs and reviews data to ensure GMP compliance.

You'll help validate and transfer analytical methods, investigate lab events, write SOPs, maintain training compliance, and manage supplies while driving continuous improvement.

Qualifications

  • Requires a BS/BA in Life Sciences or related field.
  • Minimum of 2 years of relevant industry experience as a QC Analyst.
  • Experience reviewing analytical testing in a GMP‑regulated lab is preferred.
  • Strong organizational, communication, and teamwork skills with a commitment to quality.

Responsibilities

  • Perform testing according to approved procedures to support product release and stability.
  • Review laboratory testing documentation and data for GMP compliance and quality standards.
  • Support validation, qualification, and transfer of analytical methods and procedures.
  • Investigate lab events and collaborate with cross‑functional teams to resolve issues.
  • Write, revise, and maintain controlled test procedures and SOPs.
  • Participate in training activities and maintain training compliance.
  • Manage laboratory supplies and materials for routine operations.
  • Support continuous improvement initiatives to enhance lab performance.

Skills

GMP knowledge
Documentation review
Analytical testing
Problem solving
Attention to detail
Written & oral communication

Education

BS/BA in Life Sciences or related field

Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a QC Analyst (Drug Product) to join our QC Chemistry, Drug Product Testing team.



When & Where:


  • Shift Requirements: 12/7 or Days

  • Location: Raheen, Limerick



What You'll Do:


  • Perform testing in accordance with approved procedures to support product release and stability programs.

  • Review laboratory testing documentation and data to ensure compliance with GMP requirements and quality standards.

  • Support the validation, qualification, and transfer of analytical test methods and procedures.

  • Investigate laboratory events and collaborate with cross-functional teams to support fact‑finding and resolution activities.

  • Write, revise, and maintain controlled test procedures and standard operating procedures (SOPs).

  • Participate in required training activities and maintain training compliance.

  • Manage laboratory supplies and materials required for routine operations.

  • Support continuous improvement initiatives and projects that enhance laboratory performance and efficiency.



The Environment and Physical Rhythms of This Role:


  • Thrive in a fast-paced, quality‑focused laboratory environment.

  • Quickly learn new techniques, procedures, and technologies while working independently.

  • You possess strong trouble‑shooting and problem solving skills.

  • You have strong attention to detail & excellent written and oral skills.



Let's Find Out if We're a Fit:


  • Requires a BS/BA in Life Sciences or a related field.

  • QC Analyst: Minimum of 2 years of relevant industry experience.

  • Previous experience reviewing analytical testing performed within a GMP‑regulated laboratory environment is preferred.

  • Strong organizational, communication, and teamwork skills with a commitment to quality and compliance.



Thrive today. Grow tomorrow.


#IRELIM #JOBSIEST #LI-Onsite #REGNIRLQC


We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.



Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.



Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.



As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.



For jobs in Canada: this posting is for an existing position.



Salary Range (hourly)

€18.34 - €28.70

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

QC Analyst (Drug Product)
QC Analyst (Drug Product)

Regeneron Pharmaceuticals • Limerick

On-site
EUR 25,000 - 39,000
QC Analyst (Drug Product)
QC Analyst (Drug Product)

Regeneron • Limerick

On-site
EUR 25,000 - 40,000
Temp QC Analyst - Bioassay
Temp QC Analyst - Bioassay

Biopharma Careers • Limerick

On-site
EUR 36,000 - 54,000
Sr QA Validation Specialist
Sr QA Validation Specialist

Regeneron Pharmaceuticals, Inc • Munster

On-site
EUR 54,000 - 88,000
Senior QA Specialist
Senior QA Specialist

Regeneron • Limerick

On-site
EUR 54,000 - 89,000
Senior QA Specialist
Senior QA Specialist

Regeneron Pharmaceuticals • Ireland

On-site
EUR 54,000 - 88,000
Senior QA Specialist
Senior QA Specialist

Regeneron Pharmaceuticals • Limerick

On-site
EUR 54,000 - 88,000
Principal QA Specialist
Principal QA Specialist

Regeneron Pharmaceuticals, Inc • Munster

On-site
EUR 63,000 - 104,000
Temp QA Specialist
Temp QA Specialist

Regeneron Pharmaceuticals • Limerick

On-site
EUR 55,000 - 75,000
Supervisor Quality Control (Microbiology)
Supervisor Quality Control (Microbiology)

Regeneron Pharmaceuticals, Inc • Munster

On-site
EUR 54,000 - 103,000
Annual bonuses or other incentive plan
Equity awards
Pension or retirement benefits
+4