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Supervisor Quality Control (QC Support)

Co. Limerick, Ireland
Start date
10 Jun 2024
Closing date
10 Jul 2024

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Quality, QA / QC
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Job Details

Within this role you will be responsible for the oversight of QC Critical Materials, QC Reference Standards and QC Supply functional area activities, including oversight of the Vendor Management Inventory (VMI) program. Openly communicates with Regeneron Procurement, Regeneron WHL, internal QC Lab Managers, VMI provider Management and staff. Fosters a culture of customer service for all internal and external clients.

As a Supervisor within the QC Support team, a typical day might include, but is not limited to, the following:
  • Supervising QC Critical Materials Regeneron personnel and processes
  • Supervising QC Lab Supply personnel and processes
  • Being responsible for QC Reference standard personnel and processes
  • Overseeing the third-party VMI team
  • Working with members of QC Labs, and Business Partners for reagent forecasting
  • Providing excellent customer service
  • Ensuring work is performed to quality standards
  • Evaluating and documenting deviations in the appropriate Quality System
  • Preparing and tracking metrics and providing regular data updates to management and others as required
  • Leading, supervising, and coordinating the improvement effort of streamlining processes.
  • Collaborating with the global ref std team to ensure the reference standard program is compliant with regulatory requirements
  • Collaborating with the global ref std team to ensure the implementation of laboratory reference standards for each product candidate, including material selection and preparation
  • Collaborating with the global reference standard team to ensure adequate qualification and stability testing are performed for laboratory reference standards
  • Ensuring reference standard inventories are sufficient to support testing demands
  • Working with Procurement to manage the supply of all categories of laboratory chemicals and components and participating in procurement-related activities for other categories of spend in support of the QC department
  • Being responsible for developing and implementing solutions to QC Procurement issues

This role might be for you if:
  • You excel in a fast-paced environment, capable of managing multiple projects and priorities, ensuring that all tasks are completed accurately and on time
  • You are a strong communicator and collaborator, able to work effectively with both internal teams and external partners, including global teams and third-party vendors
  • You are knowledgeable about regulatory requirements, with experience ensuring compliance with cGMPs, quality systems, and other regulatory standards, particularly in relation to laboratory reference standards and procurement activities
  • You are proactive in problem-solving, with a track record of developing and implementing effective solutions to QC procurement issues and streamlining processes for better efficiency.
  • You are interested in working closely with Procurement to manage the supply of laboratory chemicals and components and have experience or a strong interest in procurement and supply chain management within a QC context

To be considered for this opportunity you should hold a BS/BA in biochemistry, chemistry, biology or related field and 5+years of experience working in a GMP lab or equivalent combination of education and experience.


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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