RP
Head of Regulatory Affairs – Pharmaceutical Approval (m/f/d)
Dresden, GermanyPosted 21 days agoFull-time
Job details
Company
ROTOP Pharmaka GmbH
Location
Dresden, Germany
Employment type
Full-time
Seniority
Manager
Primary category
Compliance & Regulatory Affairs
Secondary category
Pharmacy & Pharmaceutical
Posted date
15 Apr 2026
Valid through
Job description
Your chance with us
Would you like to join an internationally active company in a future-proof industry? Due to our continuous growth, we are offering a permanent position in a modern work environment surrounded by nature (01328 Dresden). As Head of Regulatory Affairs – Pharmaceutical Approval (m/f/d), you can expect challenging tasks, flexible work schedules, and attractive benefits for an optimal work-life balance.More than just a job
- A permanent position in a future-proof, internationally active company
- Flexible work schedules for the best work-life balance
- 30 vacation days for relaxation
- 10 paid sick days for children to support your family
- Modern workplace (e.g., height-adjustable desks) surrounded by greenery
- Company parking and e-charging options
- 3 goodwill days/K.O. days
- Access to a diverse selection of attractive benefits via our ROTOP Benefit Portal
- Job-Rad and Jobticket for sustainable mobility
- Team-building company events to foster a strong sense of unity
- Diverse career and development opportunities and additional benefits
Your tasks
- Technical and managerial leadership of the Regulatory Affairs department
- Development and implementation of regulatory strategies for national and international markets
- Overall responsibility for regulatory dossiers, including submission, maintenance, and renewal
- Management of regulatory processes and communication with national and international authorities
- Monitoring of regulatory requirements and evaluation of new legal developments in the field of pharmaceutical regulation
- Leadership, development, and advancement of the Regulatory Affairs team, as well as close collaboration with Quality Assurance, Production, Medical Affairs, Pharmaceutical Development, and Business Development
Your profile
- A successfully completed degree in Pharmacy, Chemistry, Biology, Human Medicine, or a comparable natural science program
- Several years of professional experience in Regulatory Affairs within the pharmaceutical industry
- In-depth knowledge of national and international regulatory requirements in the field of pharmaceutical approval
- Proven experience of several years in team leadership and managing complex projects
- Strong strategic thinking and a structured, solution-oriented approach to work
- Excellent communication skills, confident demeanor when dealing with regulatory authorities and internal stakeholders, and fluent written and spoken German and English