Associate Director, CMC Regulatory Affairs (Biologics) (Remote)

Position Summary

The Senior Manager, CMC Regulatory Affairs is responsible for providing strategic and operational regulatory leadership for Chemistry, Manufacturing, and Controls (CMC) activities across development and commercial programs. This role leads the development and execution of global CMC regulatory strategies to support clinical development, marketing applications, and lifecycle management activities for biologic products, with a strong focus on late-stage development, Phase 3 programs, and rare disease therapeutics.

The Senior Manager serves as the primary CMC Regulatory Affairs representative on cross-functional teams and partners closely with Technical Operations, Process Development, Pharmaceutical Development, Manufacturing, Quality, Analytical Development, Supply Chain, Regulatory Operations, and Project Management to ensure alignment of CMC development plans with global regulatory requirements and business objectives.

This position requires extensive experience supporting biologics development programs and a strong technical understanding of biologic drug substance and drug product manufacturing, analytical characterization, process development, comparability, and control strategies. The individual will be responsible for driving CMC regulatory submissions, managing Health Authority interactions related to CMC topics, assessing regulatory risks, and supporting successful product approvals and post-approval activities worldwide.

Responsibilities

CMC Regulatory Strategy, Submissions & Dossier Development

• Develop and implement global CMC regulatory strategies to support clinical development, registration, commercialization, and lifecycle management of biologic products.
• Serve as the CMC Regulatory lead on cross-functional program teams, providing strategic regulatory guidance throughout product development.
• Assess regulatory risks, develop mitigation strategies, and provide regulatory recommendations to support program goals and business priorities.
• Contribute to regulatory strategy development for expedited development programs, orphan drug products, and rare disease indications.
• Lead preparation, review, and submission of CMC documentation for global regulatory filings, including INDs, IMPDs, CTAs, BLAs, NDAs, MAAs, amendments, supplements, variations, and annual reports.
• Author and review Module 2 and Module 3 content and ensure consistency across submission components.
• Coordinate cross-functional contributions to CMC regulatory submissions and ensure compliance with global regulatory requirements and submission standards.
• Support preparation for major registration milestones, including first marketing applications and global expansion filings.
• Lead CMC‑related Health Authority interactions and support agency meetings globally.
• Support inspection readiness and regulatory assessments related to manufacturing and product quality.
• Develop global regulatory filing strategies for lifecycle management activities and post‑approval CMC changes, including manufacturing process changes, analytical method updates, specification revisions, site transfers, process validation, and comparability assessments.

Technical Leadership for Biologics Development

• Provide regulatory guidance and strategic input for biologics development programs, including monoclonal antibodies (mAbs), recombinant proteins, fusion proteins, and other complex biologic modalities.
• Collaborate with development and manufacturing teams to support regulatory strategies related to cell line development, upstream and downstream process development, scale‑up, process validation, and commercial manufacturing.
• Evaluate regulatory impact of manufacturing changes involving microbial and mammalian cell culture processes, purification operations, formulation development, fill‑finish activities, and technology transfers.
• Support development and regulatory assessment of comparability strategies for manufacturing process changes, site transfers, process improvements, and lifecycle management activities.
• Provide regulatory oversight and strategic guidance for analytical characterization programs and control strategies supporting product quality, safety, and efficacy.
• Contribute to regulatory assessment of critical quality attributes (CQAs), process parameters, control strategies, and product characterization data throughout development and commercialization.

Education/Experience Requirements

• Bachelor’s degree in a scientific discipline such as Biology, Biotechnology, Biochemistry, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field required. Equivalent combination of education and applicable job experience may be considered.
• Advanced degree (MS, PharmD, PhD, or equivalent) preferred.
• 7+ years of Regulatory Affairs experience within the biotechnology or pharmaceutical industry, including significant CMC Regulatory Affairs experience.
• Demonstrated experience supporting biologics development programs from early development through commercialization.
• Significant experience supporting Phase 3 and late‑stage development programs.
• Experience supporting global regulatory submissions, including BLAs, MAAs, NDAs, INDs, IMPDs, and CTAs.
• Extensive experience leading CMC regulatory activities for biologic products, particularly monoclonal antibodies, recombinant proteins, and other therapeutic biologics.
• Experience supporting manufacturing process development and commercialization of biologic drug substances and drug products.
• Experience participating in and leading Health Authority interactions related to CMC topics.
• Experience supporting global post‑approval change management, comparability assessments, process validation, and lifecycle management activities.

Additional Skills/Experience/Requirements

• The ideal candidate will embody Travere’s core values: Courage, Community Spirit, Patient Focus, and Teamwork.
• Comprehensive understanding of FDA, EMA, MHRA, PMDA, Health Canada, ICH, and global CMC regulatory requirements.
• Strong understanding of biologics regulatory requirements throughout product development and commercialization.
• Experience supporting products for rare diseases and/or orphan indications preferred.
• Demonstrated ability to develop and execute global CMC regulatory strategies.
• Strong knowledge of CMC development, process validation, comparability, quality systems, and lifecycle management requirements.
• Strong technical understanding of biologics drug substance manufacturing processes and downstream processing and purification technologies.
• Strong understanding of biologic drug product development including analytical methods and characterization techniques used for biologics.
• Strong understanding of critical quality attributes (CQAs), quality target product profiles (QTPPs), control strategies, and analytical comparability principles for monoclonal antibodies and recombinant protein therapeutics.
• Ability to travel up to 10% domestically and internationally.

Comp range $132-172K based on experience level