QC Analyst (Day 1)

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

Job summary

A leading biotechnology company in Ireland is seeking a QC Analyst to perform analytical chemistry testing in a cGMP environment. Responsibilities include documenting test results, complying with regulations, and conducting various tests. The ideal candidate has a BS/BA in Life Sciences and at least 2 years of relevant experience, with strong attention to detail and problem-solving skills. Shift work is required for this position.

Benefits

Comprehensive benefits

Inclusive culture

401(k) company match

Qualifications

• 2+ years of relevant experience in a cGMP environment.
• Ability to work independently or as part of a team.
• Strong attention to detail and excellent communication skills.

Responsibilities

• Perform analytical chemistry testing to support drug manufacture.
• Gather and document test results.
• Comply with regulatory requirements.
• Conduct testing on raw materials and in-process samples.
• Maintain laboratory supplies and manage specific projects.

Skills

Analytical chemistry testing

Trouble‑shooting

Problem solving

Attention to detail

Written and oral communication

Education

BS/BA in Life Sciences or related field

Job description

As a QC Analyst you will perform a wide variety of analytical chemistry testing to support in-process and bulk drug substance manufacture in a cGMP regulatory environment.

Please note this is a 24/7 shift position. The successful candidate will be required to work shift which includes days & nights.

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; reports any quality anomalies
• Complying with all pertinent regulatory agency requirements
• Participating in required training activities
• Maintaining laboratory supplies
• Conducting testing on raw materials, 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
• Owning the responsibility for maintaining a specific project
• Devising or developing new analytical methods and techniques
• Assisting in validation of methods
• Participating in establishing the transfer of methodology from R&D

This role might be for you if:

• 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

To be considered for this opportunity you should have a BS/BA in Life Sciences or related field along with 2+ years of relevant experience.

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.