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Senior Regulatory Affairs Manager - CMC (various locations)

Remote: 
Full Remote
Contract: 
Experience: 
Expert & Leadership (>10 years)
Work from: 

Offer summary

Qualifications:

10+ years of experience in regulatory affairs, Extensive knowledge of CMC writing, In-depth understanding of EU guidelines, Excellent project management skills, Strong communication abilities.

Key responsabilities:

  • Write CMC sections and scientific rationales
  • Develop and implement variations strategies
  • Coordinate CMC activities across projects
  • Liaise with global affiliates and sites
  • Identify new business opportunities
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Job description

We are looking for aSenior Regulatory Affairs Manager/Consultantwith 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global pharmaceutical environment.

This is a client dedicated project, without people management responsibility. The role can be home or office based in various European locations.

Key Responsibilities:

  • Write CMC sections (23S, 23P, 32S, 32P) and scientific rationales for regulatory submissions and responses
  • Develop and implement variations strategies based on EU guidelines
  • Coordinate CMC activities across multiple projects
  • Liaise with global affiliates and manufacturing sites
  • Provide project leadership and management
  • Ensure client satisfaction and project quality
  • Identify new business opportunities and contribute to proposal preparation



Required Qualifications:

  • 10+ years of experience in regulatory affairs
  • Extensive knowledge of CMC writing and variations strategy
  • In-depth understanding of EU guidelines (Variation, ICH, EMA)
  • Excellent project management and organizational skills
  • Strong communication abilities and client management experience
  • Ability to work independently and as part of a team
  • Proficiency in English; additional languages are a plus



Preferred Qualifications:

  • Experience with regulatory agencies (e.g., FDA, MHRA)
  • Industry-recognized certifications or advanced degrees
  • Publication history or experience presenting at industry conferences

Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/c3f0b694eaea41e8c3ed16b12f0b59ac

Required profile

Experience

Level of experience: Expert & Leadership (>10 years)
Industry :
Information Technology & Services
Spoken language(s):
EnglishEnglish
Check out the description to know which languages are mandatory.

Other Skills

  • Teamwork
  • Organizational Skills
  • Verbal Communication Skills

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