BioSpace
Associate Director, Regulatory CMC
Join to apply for the
Associate Director, Regulatory CMC
role at
BioSpace
Company Overview Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook.
Role Summary The Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is accountable for executing global CMC regulatory strategies for our programs in early and late‑stage development through and beyond approval. This position supports Dyne’s clinical registration, commercial development, and manufacturing efforts, as applicable. It partners with the manufacturing team, clinical operations, quality, other regulatory team members, and program teams. This role is based in Waltham, MA.
Primary Responsibilities
Lead CMC regulatory execution for specific programs at all stages of development
Provide strategic regulatory input to the manufacturing and quality organizations pertaining to global product development requirements
Serve as a CMC strategist and project leader for projects, providing regulatory assessments and developing regulatory strategies with input and guidance from the team and leadership
Lead the development of CMC documentation pertaining to global regulatory filings (IND, IMPD, BLA, etc.) and responses to health authority requests, including amendments to clinical and commercial manufacturing changes
Coordinate and manage global submissions, maintain product compliance, and manage change‑control related activities
Leverage both technical and regulatory knowledge to proactively mitigate risks
Serve as the regulatory affairs CMC representative in functional and team meetings
Act as the point of contact to cross‑functional teams on global regulatory CMC project/program issues
Execute regulatory policies and operational processes to deliver high‑quality regulatory submissions
Education and Skills Requirements
Minimum of a bachelor’s degree in life science or related discipline
Minimum of 7 years of experience in the biotech/pharmaceutical industry with at least 5 years in regulatory affairs in a clinical‑stage and/or commercial biotechnology company
Experience in rare disease preferred
Experience leading and developing CMC sections of biologics marketing applications preferred
Solid understanding of FDA regulatory guidance and ICH guidelines
Strong experience with CTD format and content of regulatory filings
Thorough understanding of the drug development process and the pharmaceutical industry, including global regulatory CMC requirements, guidance, accelerated regulatory review paths, and policy trends
Knowledge of EU and international regulations related to clinical and nonclinical, development a plus
Ability to work independently to manage multiple projects in a fast‑paced environment
Ability to effectively collaborate in a dynamic, cross‑functional environment to meet each program’s critical regulatory milestones
Ability to effectively communicate the regulatory strategy, risks, mitigations, and overall plans to project/program teams and senior management
Outstanding verbal and written communication skills, regulatory writing skills, and willingness to share knowledge and lessons learned with strong attention to detail
Recognized as a leader, team player, and possess a cross‑functional collaborative skill set
Ability to influence without authority
Positive team member who embodies the Dyne core values
Excitement about Dyne’s vision and mission
Pay Range: $159,000 - $195,000 USD
Equal Opportunity Statement Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
Senior Level Mid‑Senior level
Employment Type Full‑time
Job Function Legal
#J-18808-Ljbffr
Associate Director, Regulatory CMC
role at
BioSpace
Company Overview Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook.
Role Summary The Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is accountable for executing global CMC regulatory strategies for our programs in early and late‑stage development through and beyond approval. This position supports Dyne’s clinical registration, commercial development, and manufacturing efforts, as applicable. It partners with the manufacturing team, clinical operations, quality, other regulatory team members, and program teams. This role is based in Waltham, MA.
Primary Responsibilities
Lead CMC regulatory execution for specific programs at all stages of development
Provide strategic regulatory input to the manufacturing and quality organizations pertaining to global product development requirements
Serve as a CMC strategist and project leader for projects, providing regulatory assessments and developing regulatory strategies with input and guidance from the team and leadership
Lead the development of CMC documentation pertaining to global regulatory filings (IND, IMPD, BLA, etc.) and responses to health authority requests, including amendments to clinical and commercial manufacturing changes
Coordinate and manage global submissions, maintain product compliance, and manage change‑control related activities
Leverage both technical and regulatory knowledge to proactively mitigate risks
Serve as the regulatory affairs CMC representative in functional and team meetings
Act as the point of contact to cross‑functional teams on global regulatory CMC project/program issues
Execute regulatory policies and operational processes to deliver high‑quality regulatory submissions
Education and Skills Requirements
Minimum of a bachelor’s degree in life science or related discipline
Minimum of 7 years of experience in the biotech/pharmaceutical industry with at least 5 years in regulatory affairs in a clinical‑stage and/or commercial biotechnology company
Experience in rare disease preferred
Experience leading and developing CMC sections of biologics marketing applications preferred
Solid understanding of FDA regulatory guidance and ICH guidelines
Strong experience with CTD format and content of regulatory filings
Thorough understanding of the drug development process and the pharmaceutical industry, including global regulatory CMC requirements, guidance, accelerated regulatory review paths, and policy trends
Knowledge of EU and international regulations related to clinical and nonclinical, development a plus
Ability to work independently to manage multiple projects in a fast‑paced environment
Ability to effectively collaborate in a dynamic, cross‑functional environment to meet each program’s critical regulatory milestones
Ability to effectively communicate the regulatory strategy, risks, mitigations, and overall plans to project/program teams and senior management
Outstanding verbal and written communication skills, regulatory writing skills, and willingness to share knowledge and lessons learned with strong attention to detail
Recognized as a leader, team player, and possess a cross‑functional collaborative skill set
Ability to influence without authority
Positive team member who embodies the Dyne core values
Excitement about Dyne’s vision and mission
Pay Range: $159,000 - $195,000 USD
Equal Opportunity Statement Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
Senior Level Mid‑Senior level
Employment Type Full‑time
Job Function Legal
#J-18808-Ljbffr