Associate Manager, Regulatory Labeling Operations
Regeneron Pharmaceuticals Inc

Tarrytown, New York

Posted in Pharmaceuticals
about 1 month ago


This job has expired.

Job Info


The Regulatory Affairs Labeling Operations Associate Manager is responsible for the regulatory role as part of the process for coordination, development and implementation of new and revised printed labeling for assigned commercial products as well as products in full development.. This position will be a hybrid position in regards to location.
In this role, a typical day might include the following:

  • With limited guidance, manages the development, revision, preparation and internal approval of packaging artworks e.g., carton, container label, printed package insert, for assigned development products as well as marketed products. Working knowledge of industry labeling trends related to packaging and labeling content and implementation, reviewing competitor and other labeling. Interpret labeling regulations and guidance. Identifying company impact and providing recommendations as appropriate.
  • Provide functional knowledge at relevant department meetings and relevant cross functional subteams.
  • Collaborates with packaging team to ensure packaging content and artworks are compliant with internal labeling policies, standard operating procedures and worldwide health authority regulations.
  • Contribute and manage Annual Reports for assigned products.
  • Maintain and track packaging artwork lifecycle and documents in appropriate labeling repository and electronic systems.
  • Manage and review preparation of SPL.
  • Perform/manage proofreading as requested by Labeling Lead.
  • Monitor the worldwide regulation changes pertaining to Labeling regulations and assist in the maintenance of the labeling SOP and work instructions.
  • Assist labeling staff and other subteam members in labeling operations project and process management to build expertise and awareness.
  • Works under limited supervision to determine methods and procedures on new assignments and coordinates activities/providing technical guidance to others.
  • Work under limited supervision across multiple areas.
  • Bachelor's degree (BS) from an accredited college or university, preferably in the field of Health/Science OR 4+ years of industry experience.
  • Demonstrates workingknowledge of worldwide Regulatory Agencies, industry practice, packaging manufacturing process, and drug development process, including. FDA, EMEA, and international packaging regulations and industry practices for biologic and combination product.
  • Good working knowledge of Microsoft Office applications.
  • 4 years of experience with 2 or more within in the regulatory labeling and packaging area.
  • Demonstrates the ability to contribute to the development of department strategy, operational objectives, and matters of significance.
  • Ability to contribute to resolving issues where the analysis of situations or data requires an evaluation of intangibles or situations with minimal precedent.
  • Collaborate with team members to develop innovative business solutions.
  • Working knowledge of the labeling/packaging process and related issues in medical safety regulatory and/or corporate.
  • Contribute to the Packaging Team to address packaging issues, develop plans of action, and oversee completion of packaging project.
  • With limited supervisor support, proactively share information with peers and generate discussion to resolve complex issues.
  • Manage multiple projects and prioritize work with limited supervision.
  • Attention to detail and strong organizational skill.
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.


This job has expired.

More Pharmaceuticals jobs


AstraZeneca
New York, New York
Posted about 1 hour ago

AstraZeneca
Philadelphia, Pennsylvania
Posted about 1 hour ago

AstraZeneca
West Chester, Ohio
Posted about 1 hour ago
View Pharmaceuticals jobs ยป

Job Alerts

Provide an email, zip code for jobs, and/or job category to subscribe to job alerts. Learn more now.