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 a laboratory cleanroom’s to collect and log samples for microbial analysisPerforming bioburden and endotoxin sample analysis in accordance with standard operating procedures (SOPs)Performing sample analysis for microbial identificationPerforming environmental monitoring including surface, settling and viable and non-viable particulate air monitoring of aseptic operations and controlled areasPerforming acceptance testing of commercially prepared microbiological culture media.Autoclaving microbiological media and laboratory waste as neededEnsuring that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs)Completing test records on time and peer reviews data from other analysts for accuracy and completenessAssisting in the design and set-up of the QC microbiology laboratory and selection/implementation and calibration of laboratory instrumentsParticipating in microbiological validations as needed for drug substance, in-process controls, buffers and clean utilities qualification programAssisting manufacturing personnel in the identification of microbiological root cause analysis and provide technical advice as neededParticipating in the transfer of methodology from other test facilities.Maintaining laboratory reagents, media and suppliesConducting laboratory investigations and generates reports in response to invalid assays, deviations, OOS/OOTInitiating and completes CAPAs and change controls in accordance with site procedures.Writing new and updates current SOPs as neededProviding training to other analysts in the QC groupPresenting analytical data reports clearly and concisely to managementIdentifying and implementing lab process improvements, lean initiativesPerforming other duties relevant to the QC laboratory position as required

This role might be for you if:

You have a proven ability to work independently or as part of a teamYou possess strong trouble-shooting and problem solving skillsYou have strong attention to detail & excellent written and oral skills

To be considered for this opportunity you should have a BS/BA in Microbiology or related field and 2 years of relevant 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.