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Regulatory Affairs Manager

Job in Germany, Pike County, Ohio, USA
Listing for: Beyond Trend
Full Time position
Listed on 2026-01-12
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Location: Germany

Overview

Job Title - Regulatory Affairs Manager

Terms - Full Time Role

Salary - Competitive

Job Timings – 8 AM to 5 PM

Requirements - Graduation in pharmacy background or any relevant degree

About the role
  • Supervision and motivation of national approval team members
  • Contact person for all team members
  • Proactively ensuring smooth team operations and effective collaboration
Responsibilities
  • Creating an inspiring team environment with an open communication culture and ensuring the management of authorised activities and quality records are maintained accurately
  • CAPA, Deviation, SOP drafting, training of the team, supplier audits
  • Co-ordinating with manufacturers and promptly performing any recall operations
  • Conducting supplier and customer audits as per the procedures
  • Ensuring self-inspections are performed at appropriate regular intervals with prearranged programmes and implementing corrective actions
  • Ensuring and approving final disposition of returned, rejected, recalled or falsified products
  • Approve returns to saleable stock and provide quality support and oversight for Distribution Operation review meetings with Distribution contractors
  • Contribute to defining GDP, quality, KPIs and OT review quality indicators with recommendations for improvements related to GDP guidelines
  • Ensuring CAPAs are identified, temperature control of medicines, and temperature mapping
  • Ensuring annual GDP, initial and continuous training is implemented and maintained for all employed staff
  • Ensure Quality Technical Agreements are in place for outsourced activities and with subcontractors
  • Ensure that Parallel Import design and relabeling comply with EU GDP standards
  • Maintaining required documentations and licenses for processing these licenses
  • Extensive experience in the pharmaceutical industry, with a strong background in distribution or quality assurance
  • Thorough understanding of German and EU regulations pertaining to pharmaceutical distribution, including GDP requirements
  • Excellent organizational skills with keen attention to detail and accuracy
  • Strong interpersonal and communication abilities, with the capacity to collaborate with internal and external stakeholders
  • Ability to work autonomously, manage multiple priorities, and make informed decisions in a dynamic environment
Candidate Requirements
  • Minimum 5 years of relevant experience
  • An analytical and problem-solving mindset
  • Excellent organization and time management skills
  • Commercial or pharmaceutical training
  • Good knowledge of English
  • Confident use of MS Office
  • Ability to work in a team
  • Flexibility and commitment; forward-thinking
Benefits
  • Competitive salary and performance-based incentives
  • Comprehensive benefits package including health insurance
  • Opportunities for career growth and advancement within a global organization
  • Dynamic and collaborative work environment with a diverse and inclusive culture
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