Regulatory Affairs Consultant - CMC author biologics (home or office based)

Remote Worker LTD.; Deutschland; Remote; EUR 90,000 - 150,000; Full time

Job summary

Parexel is seeking experienced CMC (Chemistry, Manufacturing, and Controls) professionals to join us as a Regulatory Affairs Consultant CMC Author to support our client. This position requires expertise in regulatory affairs, CMC authoring for initial submissions and lifecycle management, and other pharmaceutical documentation for biologics.

The role can be home or office based in various European locations.

Qualifications

• University degree in Chemistry, Pharmacy, Chemical Engineering, or related pharmaceutical field.
• 10+ years of pharma experience in CMC and regulatory affairs.
• Strong expertise in CMC for biologicals and lifecycle maintenance.
• Comprehensive understanding of ICH and EU/US guidelines.
• Experience with document management systems like Veeva.
• Fluent English; other European languages are advantageous.

Responsibilities

• Thorough understanding of the drug development process and regulatory compliance.
• Prepare CMC sections for IND/IMPDs, BLA/NDA/MAAs, and amendments.
• Write rationales to support regulatory answers and submissions.
• Coordinate CMC activities across projects and timelines.
• Understand change management and regulatory requirements.
• Develop regulatory strategies for variations and registrations.
• Support regulatory strategy for medical devices in combinations.
• Update and maintain regulatory databases with current information.
• Provide ad-hoc CMC consulting and technical advice.

Skills

Regulatory affairs

CMC authoring

Biologics expertise

Veeva

Project coordination

Education

University degree in Chemistry/Pharmacy/Related field

Tools

Veeva or similar DMS

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel is seeking experienced CMC (Chemistry, Manufacturing, and Controls) professionals to join us as a Regulatory Affairs Consultant CMC Author to support our client. This position requires expertise in regulatory affairs, CMC authoring for initial submissions and lifecycle management, and other pharmaceutical documentation for biologics. Previous experience working with biologics products is a must.

The role can be home or office based in various European locations.

Role Responsibilities

• Thorough understanding of the drug development process for all phases of pharmaceutical development and applied comprehensive understanding of regulations and guidelines to enhance probability of regulatory success and regulatory compliance.

• Thorough understanding of global regulations and ICH guidance pertaining to pharmaceutical development and lifecycle management of NCE/NME products.

• Experience preparing CMC sections of IND/IMPDs, BLA/NDA/MAAs, and supportive clinical amendments and post approval supplements/variations. (ICH Modules 2 and/or 3)

• Write scientific rationales to support regulatory answers, variations, and dossier submissions

• Coordinate CMC activities across multiple projects and manage timelines effectively

• Thorough understanding of change management processes and regulatory requirements.

• Build and assess regulatory strategies for variations and registrations based on affiliate information and EU/US guidelines

• Develop regulatory strategy for medical devices part of combination products

• Update and maintain database with current regulatory information

• Provide ad-hoc CMC consulting support and technical advice

Required Qualifications & Skills

• University degree in Chemistry, Pharmacy, Chemical Engineering, or related pharmaceutical field

• 10+ years of pharmaceutical industry experience in CMC and regulatory affairs

• Strong expertise in CMC for biologicals – initial submissions and Lifecycle maintenance

• Comprehensive understanding of ICH guidelines and EU/US regulatory guidelines

• Strong problem solving and diplomacy skills

• Ability to manage multiple projects simultaneously and meet deadlines

• Experience with Veeva or similar document management systems

• Fluent English (written and spoken); Additional European languages (French, German, Spanish) are advantageous