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This role has closed. Randstad Professional has taken the posting down.

hirly last saw it live on 28 September 2026. See similar open roles below, or browse the live board.

Randstad Professional

Regulatory Affairs Manager (f/m/d)

Ludwigshafen am Rhein, Rheinland-Pfalz, Germany

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hirly's read of this role

Role family
Healthcare
Seniority
Lead / management
Stated salary
€45,000 – €60,000 per year
Country
DE
Work mode
On-site / unstated
First seen by hirly
26 Sept 2026

Derived automatically from the posting.

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.
  • Time for change – time for a new job! You are a regulatory affairs
  • specialist and looking for a new professional challenge? Then stop
  • searching! We offer the job you are looking for: We offer a secure
  • job, fair compensation and exciting new tasks at an
  • attractive pharmaceutical company in Ludwigshafen. Apply online
  • now! We welcome applications from all suitably qualified persons
  • regardless of any disabilities.
  • 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
  • Above-average salary
  • Extensive social benefits, incl. Christmas and holiday bonuses
  • Up to 30 days vacation per year
  • Company pension scheme contribution after the end of the
  • probationary period
  • A wide range of employee benefits/perks
Original posting on Randstad Professional's site ↗

Listed on hirly, a job board. hirly is not the employer: Randstad Professional is hiring for this role.