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Regulatory CMC Writing Manager (m/f/d)
YOUR CONTRIBUTION
As a Regulatory CMC Writing Manager (m/f/d), you will be the central contact point for our manufacturing site for development and maintenance of regulatory documentation to support creation of actual regulatory dossiers. This will include the following activities:
- Preparation of CMC documentation in compliance with internal requirements and in collaboration with the manufacturing organization
- Review draft documentation with the CMC RA and the respective site
- Conduct initial impact assessments, ensures justified documentation of changes
- Provide documentation per LoQ scope and timeline, and coordinates related tasks with the manufacturing site
- Define and coordinate required information and documentation with the manufacturing site and contractors to meet agreed regulatory timelines
- Support GMP inspections as needed
- Keep current on global CMC regulations 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 of professional experience dealing with regulatory affairs aspects within the pharmaceutical industry, especially with technical writing of module 3
- Strong communication and problem-solving skills and analytical thinking ability
- Team Player with performance orientation and persistence
- Solution-oriented with a focus on compliance and quality
- Business fluent in English, German is an advantage
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 Therapeutics, a leading pharmaceutical company that helps people with movement disorders, neurological diseases, liver diseases and other health conditions regain their quality of life.
We are proud to 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 goal is 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 commitment to 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 https://www.merztherapeutics.com/.
