Regulatory Affairs Manager (mfd) CMC

Frankfurt am Main - Germany

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

YOUR CONTRIBUTION

As a Regulatory Affairs Manager (m/f/d) CMC you will apply your knowledge of global regulatory quality requirements to support the approval and maintenance of medicinal products. The position is limited to 3 years and includes the following activities:

Create review and update high-quality CMC documentation to obtain and maintain product approvals ensuring compliance with global regulatory requirements; support the creation of IMPDs for clinical trial applications
Implement change control processes coordinate regulatory assessments and maintain CMC submission and approval status
Handle and manage inquiries related to quality documentation from authorities ensuring timely and accurate responses
Oversee regulatory CMC projects communicate with Merz representatives and partners and coordinate third-party services
Develop regulatory CMC strategies and represent regulatory requirements in project teams and interdisciplinary teams
Maintain a detailed understanding of global and national CMC regulatory requirements and best practices

YOUR PROFILE

Completed scientific Studies in Pharmacy Biology Chemistry or a related field of studies a doctorate is an advantage
3-5 years in regulatory affairs or in a department responsible for CMC matters such as analytics development or quality control
Analytical and systemic thinking
Strong negotiation skills and teamwork
Solution-oriented with a focus on compliance and quality
Strong communication skills including profound English

YOUR BENEFITS

Individual career development in a purposeful job: you improve the quality of life of our patients!
Hybrid work model that allows a good work-life balance
Attractive location with good transport links modern workplaces and a company restaurant
Global family business with flat hierarchies and an open respectful corporate culture
Attractive remuneration with extensive social benefits
Variety of employer-subsidized benefits such as WellPass Deutschland-Ticket Corporate Benefits and JobBike

ABOUT US

Welcome to Merz Therapeuticsa leading pharmaceutical company that helps people with movement disorders neurological diseases liver diseases and other health conditions regain their quality of life.

We are proudto be a family-owned and value-driven company that has been dedicated to serving the needs of our patients for 110 years and is now a global innovation leader with products in more than 90 countries.

Our goalis to use our products to improve treatment outcomes for patients around the world thereby reducing the burden of suffering for affected people and their surroundings.

Our dedication and commitmentto relentless research and development is to ensure that unmet patient needs are identified and appropriate treatments are provided.

Therefore become part of our international and motivated Merz Therapeutics family now and help us achieve our goal: BETTER OUTCOMES FOR MORE PATIENTS

For more information visit Experience:

Unclear Seniority

YOUR CONTRIBUTIONAs a Regulatory Affairs Manager (m/f/d) CMC you will apply your knowledge of global regulatory quality requirements to support the approval and maintenance of medicinal products. The position is limited to 3 years and includes the following activities:Create review and update high-q...