Compliance Specialist - Engineering & Automation

Regeneron Pharmaceuticals, Inc.
Troy, NY Full Time
POSTED ON 2/5/2024 CLOSED ON 2/9/2024

What are the responsibilities and job description for the Compliance Specialist - Engineering & Automation position at Regeneron Pharmaceuticals, Inc.?

We are currently looking to fill a Compliance Specialist Engineering & Automation position. This position ensures and supports cGMP and procedural compliance for the Rensselaer Technical Operations Engineering & Automation Department. This includes conducting evaluations against documents and providing guidance to others on a variety of cGMP work.

In this role, a typical day might include the following:

  • Maintain knowledge of current good manufacturing practices (cGMPs), Biotech/Pharmaceutical industry guidance/emerging draft guides (GxP), etc. and conduct department relevant evaluations against these documents.

  • Provide support, information/guidance and assistance with the initiation, authorship, completion and follow-up of department documentation and records such as change control, investigation, root cause analysis, risk assessment, impact statement, corrective/prevention action plan, standard operating procedure/work instruction/job aid, periodic evaluation report, logbook, maintenance record/work order, lifecycle document, policies, etc.

  • Perform periodic review/evaluation of these documents and records to assess for compliance with established quality/regulatory standards/requirements, policies/guidance and procedures. Instruct/council department members in proper execution.

  • Acts as a liaison between Engineering & Automation and Quality/Regulatory groups to identify and address compliance related issues.

  • Identify opportunities for continuous improvement of compliance and support/lead improvement initiatives.

  • Support coordination activities associated with audits/inspections, author responses, and track/trend results of department quality/compliance and regulatory audits/inspections.

This role may be for you if you:

  • Strong Knowledge of cGMP biotech/pharma manufacturing operations/laboratory testing, regulatory and quality requirements/guidance, Root Cause Determination and Risk Management Techniques, procedures and documentation methods.

  • Ability to manage multiple tasks and meet deadlines.

  • Ability to speak to large groups (including senior management and regulatory agencies).

  • Ability to work independently and manage projects.

  • Excellent writing, communication and interpersonal skills.

  • Working knowledge of word processing, spreadsheet, PowerPoint and database management software.

To be considered for this role you must hold a Bachelors degree, preferably in an engineering or scientific related field, and the following minimum amounts of relevant experience for each level:

  • Assoc Specialist 0-2 years

  • Specialist 2 years

  • Senior Specialist 5 years

May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and 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. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually)

$58,480.40 - $124,300.00

About the Company:
Regeneron Pharmaceuticals, Inc.


At Regeneron, we believe in the power of original thinking. Our company is built on breakthrough ideas; which is why we foster a spirit of openness, and strive to inspire from within. We are collaborative by design and driven by curiosity. Each one of us plays an active role in transforming people’s lives through our work. Regeneron’s people make us who we are, and we are truly more than a company – we’re a community.



Simply put, we’re a tight-knit group working together to change the world.



Company Size:
5,000 to 9,999 employees


Industry:
Biotechnology/Pharmaceuticals


Founded:
1988


Website:
https://www.regeneron.com/


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