Working under the Quality Assurance organization this position is responsible for ensuring IT systems, programs and quality events are robust and meet regulatory agency expectations. The position will liaise with the IT and broader QA organizations to ensure all aspects of IT related programs are in compliance with regulatory agency expectations and internal company policies and procedures.

As a QA Validation Specialist (CSV), a typical day might include, but is not limited to, the following: 

Leading compliance monitoring of area operations, including trending of failures and evaluating efficiency of corrective actions

Investigating and troubleshooting problems which occur and determining solutions for changes and/or improvements

Reviewing, editing and approving deviation notifications, investigations, and corrective actions

Reviewing, editing and approving change control and SOPs

Participating and supporting the Quality Risk Management (QRM) principles in the formal and informal risk assessment initiatives

Supporting the development, review and approval of Quality Assurance Agreements (QAA), along with the Approved Supplier List (ASL) process

Presenting and/or defending at both internal and external (regulatory) audits and presenting in a “pressure test” scenario the technical area that they are SME

Supporting quality objectives by contributing information on best practices in industry and providing recommendations on strategic plans and reviews

Staying up to date with current industry trends and regulatory requirement updates and drive changes and improvements based on trends

Presenting project and program status and metrics to Senior Management

Acting as Technical Subject Matter Expert (SME)

Some travel may be required (approximately 25%)

This role might be for you if:

You have detailed knowledge of 21CFR11 and Annex 11 as well MHRA, FDA and WHO data integrity guidelines

You have solid understanding and experience with Computer Systems Validation and/or IT Auditing

You have an understanding of the interdependencies of change management, deviation and continuous improvement

You have knowledge of global organizations, process mapping and process improvement

You are skilled in analysing information of considerable difficulty and drawing valid conclusions

You are comfortable navigating ambiguity with the ability to help define actions

To be considered for this position you must hold a BA/BS degree. For Specialist level you must a 3+ years of related experience. Senior Specialist requires a minimum of 5 years directly related experience within Pharma or Biotech or equivalent combination of education and experience. Recent experience in a data integrity role is preferred. 

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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.