QC Micro Analyst

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Limerick
In-Office
Biotech • Pharmaceutical
The Role

Within this role you will perform testing to ensure cGMP compliance in the manufacturing facility. Responsible for assessing the microbiological quality of products, manufacturing equipment, manufacturing process areas, and facility utilities.

Note, this is a shift based role (12/7 - extended days)

As a QC Micro Analyst a typical day might include, but is not limited to, the following:

  • Entering laboratory clean-rooms to collect and log samples for microbial analysis.

  • Performing bioburden and endotoxin sample analysis in line with standard operating procedures (SOPs).

  • Performing sample analysis for microbial identification.

  • Performing environmental monitoring, including surface, settling, and viable and non-viable particulate air monitoring of aseptic operations and controlled areas.

  • Performing acceptance testing of commercially prepared microbiological culture media.

  • Autoclaving microbiological media and laboratory waste as needed.

  • Ensuring all work is carried out in compliance with regulatory standards, company policies, and SOPs.

  • Completing test records on time and peer reviewing data from other analysts for accuracy and completeness.

  • Assisting in the design and setup of the QC microbiology laboratory and selecting, implementing, and calibrating laboratory instruments.

  • Participating in microbiological validations for drug substances, in-process controls, buffers, and clean utilities qualification programs.

  • Assisting manufacturing personnel in identifying microbiological root causes and providing technical advice as needed.

  • Participating in the transfer of methodologies from other test facilities.

  • Maintaining laboratory reagents, media, and supplies.

  • Conducting laboratory investigations and generating reports in response to invalid assays, deviations, OOS/OOT.

  • Initiating and completing CAPAs and change controls in adherence with site procedures.

  • Communicating analytical data reports clearly and concisely to management.

  • Identifying and implementing lab process improvements and lean initiatives.

This role might be for you if:

  • You have a consistent record 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 or equivalent experience in Microbiology or related field and 2+ years of validated experience, or equivalent combination of education and experience.

#LI-Onsite #REGNQC #JOBSIEST #IRELIM

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

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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The Company
HQ: New York, New York
15,000 Employees
Year Founded: 1988

What We Do

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.

Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media.

An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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