Associate Manager Quality Compliance

Posted 6 Days Ago
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Limerick
7+ Years Experience
Biotech • Pharmaceutical
The Role
As an Associate Manager Quality Compliance at Regeneron, responsibilities include ensuring compliance with quality standards, overseeing quality systems, managing risk assessment activities, participating in audits, and collaborating with departments for compliance. The role requires a BSc/BEng in a scientific discipline and 7+ years of relevant experience in the pharmaceutical industry.
Summary Generated by Built In

This is a leadership role providing Quality and Compliance oversight of site operations inclusive of but not limited to Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Materials Handling, and QA Validation in accordance with mandated regulatory requirements and site expectations.

As a Associate Manager Quality Compliance, a typical day might include, but is not limited to, the following: 

  • Ensuring compliance with all aspects of Quality for the Raheen site inclusive of manufacturing, quality systems, quality control, validation, facilities and materials management

  • Overseeing site quality systems including but not limited to; Deviations, CAPA, Change Control, Audits (Internal and External) and Customer Complaints

  • Being responsible for review and approval of the following types of documents, relating to area functions: failure investigations, change control documents, corrective/preventative action documents, standard operating procedures

  • Approving procedures, policies and other instructional documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements

  • Monitoring and trending metrics for site quality systems

  • Managing and developing site risk assessment activities and site risk register

  • Participating in continuous improvement initiatives

  • Participating in regulatory and customer audits

  • Collaborating with functional departments to resolve issues and maintain compliance

  • Identifying gaps in systems and developing feasible plans for correction

  • Training of personnel on quality system processes

This role might be for you if:

  • You have the ability to work independently or as part of a team

  • You have experience leading and managing teams

  • You are a self-starter with the ability to operate in a multifaceted environment,

  • You are comfortable working on your own initiative

  • You demonstrate expert GMP knowledge


To be considered for this position you should have a BSc/BEng in a scientific discipline or related field with 7+ years of relevant work experience in the pharmaceutical or other related industry.

#JOBSIEPR #LI-Onsite #REGNIEQA  #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.

The Company
HQ: Rensselaer, New York
15,000 Employees
Hybrid Workplace
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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