Randstad Professional
67059 Ludwigshafen am Rhein - Deutschland
Regulatory-Affairs-Manager/in
Arbeit
Vollzeit
ab 05.03.2026
Beschreibung
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 sp... weiter lesen
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 sp... weiter lesen
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
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
Ref-Nr.: 9696722
Aktualisiert:
04.03.2026
Quelle: Bundesagentur für Arbeit
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Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
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