The Staff IT Compliance Analyst is responsible for ensuring that the manufacturing IT group is operating in compliance with regulatory requirements and Regeneron internal procedures and manage the internal and external audits.
As a Staff IT Compliance Analyst, a typical day might include the following:
* Provide expert analysis and guidance to manufacturing IT team in regulatory/quality related area and manage an internal program to prepare for internal and external audits readiness.
* Evaluates, develops and modifies manufacturing IT Policies and Standard Operating Procedures plus company practicies to meet regulatory and corporate requirements and obligations.
* Represents and assists manufacturing IT SMEs during internal and external audits and lead the responses to audit findings.
* Establish, maintain and improve metrics to track IT compliance & Inspection Readiness and communicate those findings.
* Work collaboratively with our global sites to ensure systems deployed are managed and supported to meet the compliance expectations/requirements of the business while champoining Data Integrity.
* Monitor industry wide trends in audit observations, assess gaps if any and take appropriate timely actions.
* Performing other duties assigned by IT management, demonstrating flexibility and a broad understanding of IT functions. (e.g. IT Deviations, IT Change Controls, Creating/Updating IT Documents)
This role may be for you if you have:
* A deep understanding of GXP regulations (FDA 21 CFR Part 11, EU Annex 11) and IT systems Validation/qualification.
* 3+ years of experience with IT systems used in regulated environments.
* 5+ years of experience in IT Compliance within biotechnology or pharmaceutical industry.
In order to be considered for this position, you must hold a BS/BA in Information Technology or related field required along with
* 10 years of relevant experience.
* 12 years of relevant experience.
* May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.
* Quality Assurance (QA) experience strongly desired.
* Experience in the pharmaceutical or biotechnology industry preferred.
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.
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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