QC Analyst (HPLC)

Regeneron Pharmaceuticals, Inc; Munster; On-site; EUR 80,000 - 100,000; Full time

Job summary

A leading biopharmaceutical company in Munster, Ireland seeks a QC Analyst with HPLC expertise to perform chemical and biological analyses. The role involves documenting results, ensuring regulatory compliance, and participating in training activities. A BS/BA in Life Sciences and minimum 2 years' experience in QC is required. Ideal candidates will have strong attention to detail and problem-solving skills. The position offers competitive benefits and a collaborative work environment.

Benefits

Health and wellness programs

401(k) company match

Paid time off

Qualifications

• Minimum of 2 years' experience in QC.
• Experience in SE-UPLC, peptide and glycan assay is desirable.
• Ability to work independently or as part of a team.

Responsibilities

• Perform chemical or biological analyses on products.
• Document test results and ensure compliance with standards.
• Maintain laboratory supplies and conduct various tests.

Skills

HPLC experience

Troubleshooting

Attention to detail

Problem solving skills

Education

BS/BA in Life Sciences or related field

Tools

HPLC

UPLC

Empower

Job description

As a QC Analyst in HPLC Chemistry you will perform a wide variety of chemical or biological analyses on products, in-process materials, or stability samples in support of the company’s quality program.

In this role a typical day might include, but is not limited to, the following:

• Gathering data and documenting test results
• Reviewing test results to ensure compliance with standards and reporting any quality anomalies
• Complying with all pertinent regulatory agency requirements
• Participating in required training activities
• Maintaining laboratory supplies
• Conducting testing on in-process, product, stability, and/or research samples
• Writing and revising control test procedures and SOPs
• Completing test records and reviewing data
• Calibrating or verifying calibration of instruments/devices prior to use
• Interacting with outside customers or functional peer groups
• May be responsible for maintaining a specific project
• May devise or develop new analytical methods and techniques
• May assist in validation and method transfer of methods
• May be involved in establishing the transfer of methodology from R&D

This role might be for you if:

• You have current or prior experience working with HPLC in a regulated environment
• You enjoy working a shift pattern
• You have a proven ability to work independently or as part of a team
• You possess strong trouble‑shooting and problem solving skills
• You have strong attention to detail & excellent written and oral skills

Qualifications

To be considered for this opportunity you should have a BS/BA in Life Sciences or related field. Minimum of 2 years’ experience in QC. HPLC/UPLC and Empower required. Experience in SE‑UPLC, peptide and glycan assay desirable.

#IRELIM #JOBSIEST #LI-Onsite #REGNQC

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.