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Director, Quality Auditing (GMP)

Employer
Regeneron Pharmaceuticals, Inc.
Location
Troy, New York
Start date
Aug 14, 2022

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Discipline
Quality, Quality Control
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Pharm Country, Best Places to Work
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Job Details

We are currently looking to fill a Director of Quality Auditing position. This position will be responsible for providing professional expertise, leadership, oversight and planning for the Regeneron Quality Auditing function, with primary emphasis on GMP, IT and Quality audits that may impact GMP operations and/or product. Quality (GMP) Auditing is responsible for maintaining the internal and external audit programs and performing audits for Regeneron.

The work location is onsite at Regeneron's Rensselaer, NY facility - not a remote based opportunity.

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

  • Maintaining professional expertise and knowledge of audit criteria including, but not limited to, internal company policies and procedures, and applicable local and international regulations, standards and guidelines (e.g., Chapter 21 of the Code of Federal Regulations, Eudralex Volume 4 and associated Annexes, ISO Standards, and ICH, WHO and IPEC Guidelines, etc.)

  • Supervising and presenting industry trends as they relate to regulatory agency findings, expectations and warning letters

  • Collaborating with Procurement, External Manufacturing, Drug Product Quality, QA & Operations and other team members and audit clients pertaining to supplier audits

  • Leading all aspects of the audit programs and audit schedules for GMP/Quality and IT audits

  • Strategically planning, prioritizing and handling resources to meet audit schedules, company and departmental goals and objectives, and quality standards

  • Providing direction on auditing matters, and providing leadership, mentorship and supervision to auditing personnel; promote a GxP and Quality approach

  • Planning, leading, performing and/or supervising audits

  • Handling the selection, training, onboarding and biennial assessment of proxy auditors

  • Coaching, developing and mentoring employees to drive succession planning and business continuity planning

  • Compiling, organizing, and communicating auditing Right to Operate (RTO) metrics to senior management

  • Ensuring the training and qualification program for GMP Auditing employees is appropriate and adequately maintained

  • Reassessing auditing processes and procedures periodically for continuous improvement opportunities to ensure optimal performance; continually improve in a strategic and thoughtful manner

This role may be for you if you:

  • Have 10 years of proven experience leading a GMP auditing team

  • Can ensure auditing processes and procedures meet the minimum regulatory requirements and ensure current industry standards and expectations and are followed

  • Enjoy being accountable for the performance and results of the Quality (GMP) Auditing Department

To be considered for this role you must hold a Bachelor’s degree in a life sciences subject area or related field (chemistry, biology, or pharmacy preferred) and the following amount of pharmaceutical/biotechnology industry experience, including experience with Quality Systems and auditing for each level:

  • Associate Director: 10+ years

  • Director: 12+ years

Level to be 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 amazing benefits including health and wellness programs, fitness centers and stock for 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 maternity 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.

#REGNQA

Company

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to seven FDA-approved treatments and numerous product candidates in development, all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye disease, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, infectious diseases, pain and rare diseases.
 
Regeneron is accelerating and improving the traditional drug development process through our proprietary VelociSuite® technologies, such as VelocImmune® which produces optimized fully-human antibodies, and ambitious research initiatives such as the Regeneron Genetics Center, which is conducting one of the largest genetics sequencing efforts in the world.

Stock Symbol: REGN

Stock Exchange: NASDAQ

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Find Us
Website
Phone
914-847-7000
Location
Corporate Headquarters
777 Old Saw Mill River Road
Tarrytown
New York
10591
United States
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