Randstad Professional
Regulatory Affairs Manager (f/m/d)
Ludwigshafen am Rhein, Rheinland-Pfalz, Germany
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hirly's read of this role
- Seniority
- Lead / management
- Stated salary
- €45,000 – €60,000 per year
- Country
- DE
- Work mode
- On-site / unstated
- First seen by hirly
- 30 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
- Randstad is one of the world's leading talent companies with the
- ambition to be the world's most equitable and specialized talent
- company. Through our "partner for talent" corporate strategy, we find,
- develop and connect specialized talents with companies - worldwide,
- locally and always at a high speed. We build high-quality, diverse,
- and agile teams, while individuals can enjoy a rewarding career path
- with equitable opportunities.
- Randstad Professional is one of Randstad's four specializations
- and focuses on the placement of specialists and managers in the
- future-oriented sectors of IT, Engineering, Life Science and Office.
- Regulatory affairs specialist at
- a pharmaceutical company in Ludwigshafen wanted! Are you
- interested? With the many benefits such as competitive compensation
- and retirement plans, you certainly can't say "no". If that's
- the case, apply today for the available position! Here's another
- advantage: Applying with us is absolutely straightforward, requiring
- only your name, email address, and resume. People with disabilities
- are warmly welcomed at our company.
- Provide support to complete product dossiers, technical files and
- responses to information requests
- Coordinate and complete documents required by federal agencies,
- incl. maintaining complex files and electronic document management
- systems
- Work with project teams to obtain approval for company products
- Serve as the primary point of contact for federal governmental
- agencies, embassies and consulates in Germany and function as center
- of excellence for requests
- Gather documents from all EU facilities required for product
- registration in applicable countries/regions
- Coordinate document requests for products approved via the
- Centralized Procedure (CP) but are manufactured in Germany
- Work directly with third party manufacturing companies to obtain
- documents
- Bachelor's degree in life science, clinical research studies or
- engineering, ideally with previous regulatory experience
- Several years of experience in a regulated business environment
- (e.g. legal office, regulated industry)
- Experience working with Microsoft Office suite, most notably with
- Excel, Word, Outlook, Teams, and Microsoft SharePoint tools
- Working knowledge of database management
- Knowledge on current policies and practices issued by local German
- federal agencies
- Awareness on regulatory policies/procedures to learn and better
- understand how the landscape of regulations develops
- Good proficiency in the English language
- Strong negotiation and communication skills as well as ability to
- organize data and identify issues or gaps in documentation
- Performance-based salary package depending on qualifications and
- professional experience
- Option of permanent employment with our business partner
- Up to 30 days vacation per year
- Candid corporate culture
- A wide range of employee benefits/perks
Listed on hirly, a job board. hirly is not the employer: Randstad Professional is hiring for this role.
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