Job Description

CMC Regulatory Consultant - Permanent

  • Salary: Competitive
  • REF Number: v-174056
  • Consultant: Hendre Moolman
  • Contact: 01438842970
  • Date Published: 09.02.2026
  • Industry: Pharmaceutical
  • Location: Munich, Germany
  • Functional Expertise: Regulatory Affairs

Title: CMC Regulatory Consultant

Location: Munich, Germany (1–2 days remote working)

Position: Permanent opportunity

Rate: Competitive market salary

CK Group are recruiting on behalf of a science-led pharmaceutical and biotechnology consultancy providing expert CMC, quality, and regulatory support across drug development.

The Role: This is a client-facing CMC Regulatory Consultant position, acting as a technical and quality expert across a broad range of drug substances and drug products. The role covers CMC and quality topics from pre-clinical development through to approved commercial products, working closely with internal experts, clients, and external partners.

Key Responsibilities:

  • Provide scientific and regulatory advice on CMC and quality aspects of drug development.
  • Ensure CMC work packages and documentation are phase-appropriate and aligned with regulatory expectations.
  • Prepare quality sections for regulatory submissions, including IND, IMPD, BLA, NDA, and MAA.
  • Perform gap analyses on client CMC packages and develop mitigation strategies.
  • Support due diligence activities.
  • Prepare briefing packages and participate in regulatory agency meetings, including scientific advice and milestone meetings.
  • Manage operational and strategic interactions with CDMOs.
  • Coordinate filing activities across cross-functional teams and external contributors.
  • Maintain awareness of evolving regulatory guidance and requirements.
Audit Coordination:
  • Support quality and CMC readiness for regulatory submissions and inspections.
  • Contribute to structured review, follow-up, and coordination of quality documentation.
  • Liaise with internal teams and external partners to ensure compliance with regulatory expectations.
Your Background:
  • PhD or Master’s degree in Pharmacy, Chemistry, Biopharmaceuticals, Biochemistry, Biology, or a related discipline.
  • At least five years’ experience in CMC development or CMC regulatory affairs within a scientific or technical environment.
  • Hands-on experience with regulatory filings such as IND, IMPD, BLA, NDA, or MAA.
  • Strong understanding of CMC and regulatory requirements across all development stages.
  • Confident communicator in English; German language skills are an advantage.
  • Comfortable working in a collaborative, client-focused consulting environment.
  • Willingness to travel moderately for client, agency, or CMO meeting.
Apply:

Please send your CV and cover letter in English. It is essential that applicants hold entitlement to work in Germany, or make it clear if a visa is required. Relocation support is provided. Please quote job reference 174056 in all correspondence.

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