Menu

Director, Global Labeling Regulatory Affairs

at Incyte Corporation in Wilmington, Delaware, United States

Job Description

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.

The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.

Job Summary (Primary function)

The Dir, Global Labeling Regulatory Affairs leads the labeling function within Regulatory Affairs and will be accountable for delivering high quality and compliant labeling for products across our portfolio. The Dir holds both a strategic and operational role, focused on the development and implementation of an efficient, robust, compliant and global labelling process. This includes products under development and maintenance of marketed products. The Dir works in collaboration with the cross-functional development team to define appropriate labeling strategies and ensure regulatory requirements are met to deliver timely approvals.

Essential Functions of the Job (Key responsibilities)

Establish and implement the labeling function for development and post-approval phases, including development of relevant systems, processes, and procedures.

Define appropriate regulatory labeling strategies and recommends labeling language for submission to the targeted regions.

Manage/organize the labelling committee and keeps oversight of company core data sheet (CCDS).

Advise teams on the regulations, guidance, and industry best practices related to product labeling.

Evaluate and define regulatory labeling requirements needed for approval and marketing in targeted regions.

Provide regulatory labeling support to cross-functional project teams.

Responsible for coordinating the preparation and review of product specific information for regulatory submissions.

Support product teams during labeling discussions with regulatory authorities; liaise with health authorities, as needed (e.g. telephone contacts, teleconferences, meetings, submissions).

Establish and maintain a system for the appropriate retrieval, distribution and archive of product labeling to support internal and external requirements and support audits/inspections.

Partner effectively across the organization including, but not limited to, R&D, Pharmacovigilance, Manufacturing, Supply Chain, and Commercial.

Qualifications (Minimal acceptable level of education, work experience, and competency)

Bachelors or advanced degree (Ph.D. or Pharm.D.) in scientific/life-sciences or related field.

A minimum of 8-10 years' experience in regulatory affairs with at least 5 years specific to labeling.

Strong knowledge of regulations/guidelines governing development of pharmaceutical product labeling; experience in working with international regulatory agencies; working knowledge of systems/processes for labeling documentation management.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

We Respect Your Privacy

Learn more at:

The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.

 

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process .

You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.

You can learn more about Incyte's data protection practices . By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte,... For full info follow application link.

 

We appreciate, celebrate, and thrive on one another’s differences and strengths and are proud to be an Equal Opportunity Employer. By valuing diversity of backgrounds and perspectives and prohibiting all forms of harassment, we are able to promote a collaborative and innovative work environment in which everybody can contribute to their fullest potential.        

        

 

Job Details

Company

Incyte Corporation

Location

1801 Augustine Cutoff
Wilmington, Delaware 19803
United States

Copy Link

Job Posting: 810985

Posted On: Jun 07, 2021

Updated On: Jul 01, 2021