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Director, Regulatory Affairs Cmc

Propharma
Propharma
7+ years
Not Disclosed
Remote, USA, Remote
10 May 6, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About ProPharma

For over 20 years, ProPharma has improved patient health and wellness by providing expert guidance to biotech, medical device, and pharmaceutical organizations. Through its advise–build–operate model, ProPharma supports clients across the full product lifecycle.

Core Expertise

  • Regulatory Sciences

  • Clinical Research Solutions

  • Quality & Compliance

  • Pharmacovigilance

  • Medical Information

  • R&D Technology

ProPharma delivers fully customizable, end-to-end consulting solutions to reduce risk and accelerate drug and device development.


Role Overview

Position: Director, Regulatory Affairs – CMC (Chemistry, Manufacturing, and Controls)
Level: Senior (Contractor)

This role is responsible for defining and executing global CMC regulatory strategies across development programs—from early-stage development through commercialization and post-approval lifecycle management.

The Director will act as a strategic leader and subject matter expert (SME), ensuring high-quality, compliant, and globally aligned CMC regulatory submissions. The role requires strong cross-functional collaboration and the ability to independently drive complex regulatory initiatives in a fast-paced biotech environment.


Key Responsibilities

Regulatory Strategy & Leadership

  • Lead global CMC regulatory strategies across all development phases (IND, IMPD, BLA/MAA, post-approval)

  • Provide strategic regulatory guidance to Manufacturing and Quality teams

  • Identify regulatory risks and implement mitigation strategies

  • Anticipate challenges and drive proactive regulatory solutions

Submission & Compliance Management

  • Oversee planning, development, and delivery of CMC sections for global submissions

  • Ensure alignment with global regulatory requirements and evolving guidelines

  • Respond to Health Authority (HA) queries

  • Maintain regulatory compliance across product lifecycle

Cross-Functional Collaboration

  • Partner with Manufacturing, Quality, Clinical Operations, and Program Teams

  • Support clinical registration and commercial readiness

  • Coordinate global submissions and product registration activities

Change Management

  • Manage regulatory aspects of manufacturing changes (clinical and commercial)

  • Ensure compliance with global change control requirements

Knowledge Sharing

  • Contribute to organizational learning through best practices and insights

  • Stay current with regulatory trends and global policy updates


Education & Experience Requirements

Education

  • Bachelor’s degree in Life Sciences or related field (required)

  • Advanced degree (MS/PhD) preferred

Experience

  • 10+ years in biotech or pharmaceutical industry

  • 7+ years in Regulatory Affairs with strong CMC focus

  • Proven experience leading CMC sections of global submissions (BLA/MAA)

  • Experience with global regulatory filings and Health Authority interactions (e.g., FDA, EMA)

Technical Expertise

  • Deep knowledge of CMC regulatory requirements across development and commercialization

  • Strong understanding of:

    • FDA regulations

    • ICH guidelines

    • Global regulatory frameworks

  • Experience with CTD structure and global submission requirements

  • Familiarity with EU and international regulatory processes (preferred)


Core Competencies

  • Strategic thinking and problem-solving

  • Strong communication (written, verbal, executive-level)

  • Ability to influence cross-functional teams and senior stakeholders

  • High attention to detail and commitment to quality

  • Strong organizational and time management skills

  • Ability to manage multiple complex projects simultaneously

  • Independent, self-driven, and adaptable in dynamic environments


Engagement Details

  • Contract Duration: 12 months (with potential extension)

  • Engagement Type: Full-time contractor (FTE-equivalent)

  • Time Zone: EST working hours required

  • Location: Primarily remote

  • On-site Requirement: Occasional presence in Waltham, MA

  • Travel: May be required for training and key project phases


Work Environment & Culture

  • Commitment to diversity, equity, and inclusion

  • Encourages innovation, collaboration, and entrepreneurship

  • Equal Opportunity Employer ensuring a safe and inclusive workplace


Recruitment Process

  • Applications reviewed by human recruiters (no AI screening)

  • All candidates receive application outcomes


Additional Notes

  • Remote work supported; hybrid encouraged where feasible

  • No advantage/disadvantage based on proximity to office

  • No unsolicited resumes from third-party recruiters

  • No phone calls or emails regarding this posting