Medical Legal Regulatory Coordinator - Putzbrunn, Deutschland - W. L. Gore & Associates

W. L. Gore & Associates

Geprüftes Unternehmen

Putzbrunn, Deutschland

vor 2 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Tätigkeit :
Marketing & Kommunikation

Primärer Standort :
Europa-DE-BY-Putzbrunn

Reisetätigkeit : 15%

Schicht :
Frühschicht

Beschäftigungsart :
Vollzeit

Medical Legal Regulatory Coordinator (f/m/d

About Us:

Gore is a materials science company focused on improving lives through discovery, product innovation and rewarding careers for our Associates.

About the Role:

We are looking for a Medical Legal Regulatory (MLR) Coordinator (f/m/d) to join our global Medical Legal Regulatory team in EMEA.

In this role, you will coordinate Medical Legal and Regulatory approvals for advertising, promotional and training materials working with cross-functional teams (Marketing, Marketing Communications, Medical Affairs, Legal, Regulatory and others), as required.

This is a remote position, so you can work from your home office in most locations within Europe where Gore has an entity.

Responsibilities:

Change initiator for MLR approval
Host regular live meetings for stakeholders to discuss concerns or address questions
Collaborate with a Medical Legal Regulatory team members to ensure adequate global coverage
Communicate effectively and professionally with internal clients to provide a streamlined service
Provide a Medical Legal Regulatory guidance routinely to Associates who collaborate on materials for MLR approval
Review materials for legal guidance compliance
Participate in internal audits to track and oversee compliance
Share and document best practices and lessons learned to enhance overall functional and business success
Assist with onboarding and refresher training to internal and external partners on the MLR approval process

Required Qualifications:

Minimum of 3 years' experience assisting with complex deliverables under tight deadlines
Minimum of 3 years working on a team and optimizing processes around complex tasks including those related to quality system documents
Minimum of 1 year experience in a medical device or regulated environment
Demonstrated outstanding interpersonal skills including teamwork, coordination and communication as well as a close eye on attention to detail
Ability to manage and prioritize workload proactively in a fastpaced environment
Adaptable, open to change and ability to adapt in ambiguous instances
Selfmotivated with the ability to work independently
Flexible to work with different time zones
Ability to travel up to 20%
Fluent in English and or other languages

Desired Qualifications:

Medical device or other MLR/PRC (promotional review committee) experience
Experience in promotional marketing environment
Familiarity with Workfront or equivalent project management and proofing tool

*Remote Working Arrangements are permitted for Associates, with appropriate approval and compliance with Gore's remote working policies, from the country in which they are employed.

Please submit your resume in English

We believe in the strength of a diverse workforce and inclusive work environment.

In support of our values and continued success we are proud of Associates around the world who support an inclusive work environment, strive to reflect the diversity of the communities where we operate, and ensure all Associates and external partners are treated with fairness, dignity and respect.

Our Talent Acquisition Team welcomes your questions at or toll-free at

**#LI-ENL