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Temp Qc Analyst (Hplc/Micro/Tech Resource)

Posted on Feb. 17, 2026

  • Full Time

Temp Qc Analyst (Hplc/Micro/Tech Resource) job opportunity

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We are currently recruiting for a number of temporary positions within our Quality Control (QC) organisation. These roles support routine testing, assay execution, and the smooth running of laboratory operations across Microbiology, Chemistry (HPLC), and Biochemistry (Gels).

These positions are ideal for individuals with strong laboratory skills, attention to detail, and an interest in working in a regulated biopharmaceutical environment.

We have opportunities across three key QC areas:

1. QC Tech Resource Specialist - Days

Supporting day-to-day QC operations, you will help coordinate sample management, equipment readiness, documentation, and laboratory workflows. This role ensures QC teams have the resources, materials, and support required to meet testing schedules.

2. QC Micro Analyst - (Shift)

You will perform microbiological testing on in-process materials, utilities, components, and final product samples. Activities may include environmental monitoring, plate reading, bioburden testing, endotoxin, and other routine assays in line with cGMP requirements.

3. QC Analyst – Chemistry (HPLC) - (Shift)

You will perform chemical and analytical testing using HPLC and other instrumental techniques. Activities include sample preparation, system set‑up, data generation and review, and supporting release, stability, and in‑process testing using validated methods.

4. QC Analyst – Biochemistry (Gels) - (Days)

You will support biochemistry testing such as SDS‑PAGE, Western blotting, and other gel‑based or protein‑characterisation assays. Responsibilities include running assays, managing samples, reviewing results, and supporting release, stability, and in‑process testing programmes.

This is a 12-month temporary contract. Some of these positions involve working to a shift pattern.

A typical day might include, but is not limited to, the following:

  • Perform routine laboratory testing in line with SOPs, cGMP, and safety requirements
  • Complete documentation accurately and in a timely manner
  • Support assay execution, method adherence, and troubleshooting where applicable
  • Maintain equipment, manage reagents, and ensure a clean and safe workspace
  • Participate in team workflows, sample management, and testing schedules
  • Assist with investigations, deviations, CAPAs, and continuous improvement initiatives
  • Contribute to a compliant, audit-ready QC environment

This role might be for you if

  • Have experience working in a laboratory or QC environment (industry or academic)
  • Are comfortable following detailed procedures and working to high standards
  • Are organised, reliable, and able to manage your own workload
  • Have strong attention to detail and good documentation practices
  • Communicate clearly and work well within a team
  • Are interested in developing your skills across QC Micro, Chemistry, Biochemistry, or laboratory operations
  • Hold a relevant science qualification (e.g., Microbiology, Chemistry, Biochemistry, Biotechnology)

#REGNQC #LI-Onsite #IRELIM #JOBSIEST

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.
Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.

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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.


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