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Associate Manager, QA Change Control

Regeneron Pharmaceuticals, Inc.
Troy, New York
Start date
Sep 5, 2022

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

The Change Control team is hiring! The Associate Manager, QA Change Control works to facilitate process improvements, ensure training of end users, and support the Quality Management System.

As an Associate Manager, Quality Assurance, a typical day might include the following:

  • Developing and leading training for end users of the Change Control System
  • Actively seeking out opportunities for improving the Change Control System and Process based on feedback from QA, end users, and process monitoring
  • Leading Continuous Improvement activities and working with other members of the Quality Assurance team and/or end users of the system on the development and implementation of updates to the Change Control System, Process, and associated procedures
  • Developing relationships with end users and providing advice on standard methodologies in Change Control
  • Developing, monitoring, and presenting metrics to ensure the health of the Change Control System
  • Partners with counterparts to ensure global alignment of processes, systems, and procedures
  • Interpreting compliance and regulatory requirements for incorporation into departmental systems, procedures, and documentation.
  • Assisting as needed in audits and inspections
  • Review and Approval of Change Proposals as the need arises
  • Responsible for leading, mentoring and developing direct reports.

This role might be for you if:

  • Knowledgeable in Biotech/ Pharmaceutical Quality systems inclusive of cGMP, FDA regulations and familiarity with ICH guidelines and global regulatory
  • Demonstrated ability to perform independent work requiring attention to detail, accuracy and scientific judgment and a consistent record of shifting thought processes quickly from one task to another
  • Ability to comprehend, analyze and interpret process and systems information, technical procedures, reports and regulations to make decisions in GMP environment
  • Consistent track record of establishing and maintaining effective working relationships with managers and employees as well as influencing individuals of various levels to gain understanding and/or acceptance of an idea, policy, procedure, or plan
  • Possess excellent interpersonal, written and oral communication skills with the ability to apply active listening skills to understand concerns or reasoning in order to be responsive, gain trust and build strategic relationships
  • Proficient digital literacy in Microsoft (MS) Word, Excel, PowerPoint, and SharePoint required. Experience with Quality Management Systems heavily preferred

To be considered for the Associate Manager, Quality Assurance position you must have a Bachelor’s in a scientific or engineering subject area or related field with 6-8 years experience in a combination of quality, production, engineering, regulatory (chemistry, manufacturing and control) and/or laboratory, with proven accomplishments in successfully implementing cGMP requirements. Experience in change control function strongly preferred.  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 amazing benefits including health and wellness programs, fitness centers and stock 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.

#REGNQA #LI-Hybrid


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