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Senior Manager, GVP Auditing

Regeneron Pharmaceuticals, Inc.
Basking Ridge, New Jersey
Start date
May 11, 2023

View more

Administration, Accounting, General
Required Education
Bachelors Degree
Position Type
Full time
Pharm Country, Best Places to Work

Job Details

The Regeneron Senior Manager, GVP Auditing, is a key position in the Global Development Quality Assurance (GDQA) group and will provide guidance and leadership for the Good Pharmacovigilance (GVP) audit function. We believe this Sr. Manager will create strategic partnerships and implement risk-based quality auditing activities across the Regeneron Pharmacovigilance System. We Senior Manager applies expertise in GVP, GxP and international regulations to the auditing process to independently address a variety of complex GxP compliance issues. The GVP Auditor will have an expert knowledge of the FDA and EU regulations and ICH guidance documents along with any other regulations that may affect drug development and post-authorization safety monitoring. We expect the Auditor to be assigned to lead audits of higher complexity (e.g., directed audits) and is expected to have a deeper level of knowledge and experience in conducting all audit types (e.g., process, vendor, license partner, etc.). The Sr. Manager is considered a top subject matter expert who possesses an advanced knowledge of the Drug Development space. One of the key objectives for the Auditor is to support the development and execution of departmental goals and objectives and to assist with the training and mentoring of audit staff.

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

  • Responsible for “end to end” audit process which includes
  • Schedule, prepare, conduct, report and follow-up on routine and directed audits in support of their GxP discipline as directed and in accordance with Regeneron standard operating procedures and quality policies.
  • Audits include internal audits and external audits conducted globally.
  • Own the identification of internal quality/compliance issues and act as a catalyst for process improvements to promote standardization and standard processes both within GDQA and across Regeneron.
  • Represent GDQA on high value and complex teams, compliance projects and initiatives both within and across functional areas or other departments as applicable.
This role might be for you if:
  • You previously experience with European, FDA or other Regulatory Inspections of Marketing Authorization Holders or CROs.
  • You can effectively communicate across a global organization to key partners that vary in title and scope.
  • You are capable of working autonomously and navigate ambiguous situations
  • You have phenomenal project management, customer management, teamwork skills and negotiation of complex situations

To be considered, we are expecting individuals to have a Bachelor’s degree (Master’s degree preferred) with 8+ years of relevant industry experience with 5+ years of direct GVP audit experience preferred.

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)

$126,600.00 - $206,600.00


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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Corporate Headquarters
777 Old Saw Mill River Road
New York
United States

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