Director, Regulatory CMC

Rhythm Pharmaceuticals, Inc; Boston (MA); Hybrid; USD 182,000 - 275,000; Full time

Benefits offered by this job

Discretionary bonus

Benefits package

Restricted stock units (RSUs)

Hybrid work model

Job summary

Rhythm Pharmaceuticals, Inc. is seeking an experienced Regulatory CMC professional to execute high-quality, compliant CMC deliverables for assigned programs.

This individual contributor role collaborates with Global Regulatory Affairs, Technical Operations, and Quality to ensure timely, complete submissions and alignment with global requirements. The role is based in Boston with a hybrid-work model and may require some travel.

Qualifications

• Minimum a B.S. in a scientific or life sciences discipline with 10+ years in Regulatory CMC, manufacturing, analytics, quality, or related pharma environments.
• Experience supporting regulatory programs for rare diseases or high unmet medical need is preferred.
• Experience preparing CMC docs for clinical, marketing, post-approval submissions, and health authority responses.
• Experience with peptides and injectable dosage forms and/or injection drug delivery devices is required.
• Strong ability to manage multiple deliverables and meet aggressive timelines.
• Knowledge of global CMC regulatory requirements across multiple ICH regions.

Responsibilities

• Serve as regulatory CMC representative on cross-functional teams and execute deliverables aligned with strategy.
• Author, compile, review, and finalize high-quality CMC docs and submissions (core dossiers, INDs, IMPDs, MAAs, BLAs, variations, annual reports).
• Coordinate timely regulatory filings and submission activities across regions and timelines.
• Prepare regulatory CMC meeting requests, briefing materials, and supporting documents for health authorities.
• Assess CMC change controls for regulatory impact and filing requirements.
• Track commitments, questions, and actions; coordinate cross-functional responses within deadlines.
• Maintain knowledge of relevant CMC regs, guidance, and regional expectations; communicate impact to stakeholders.
• Contribute to continuous improvement of regulatory processes, templates, SOPs, and systems.

Skills

Regulatory CMC

Manufacturing

Analytical development

Quality

Cross-functional collaboration

Project management

Global regulatory knowledge

Communication

Education

B.S. in scientific or life sciences

Job description

Company Overview

Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.

Opportunity Overview

This role is responsible for executing high-quality, science-based, and compliant regulatory CMC deliverables for assigned program(s), in alignment with strategies established by Global Regulatory Affairs and Technical Operations.

This individual contributor role will execute regulatory CMC plans and support implementation of filing strategies for assigned programs. As part of the growing and dynamic regulatory affairs team, this role is accountable for the effective management and timely delivery of CMC regulatory documents, coordination of cross-functional inputs, and support of regulatory CMC execution activities across development, commercialization, and lifecycle management. The role will work closely with Global Regulatory Affairs, Technical Operations, Quality, and other internal stakeholders to ensure deliverables are aligned, complete, and compliant with global regulatory requirements and commitments.

Responsibilities and Duties

• Serve as the regulatory CMC representative on cross-functional teams for assigned programs and execute deliverables in alignment with strategies established by Global Regulatory Affairs and Technical Operations.
• Author, compile, review, and finalize high-quality CMC regulatory documents and submissions, including core dossiers, INDs, IMPDs, MAAs, BLAs, variations, and annual reports, in collaboration with internal and external stakeholders.
• Coordinate and support the timely execution of regulatory filings and submission activities in compliance with applicable global regulatory requirements, commitments, and internal timelines.
• Prepare regulatory CMC meeting requests, briefing materials, and supporting documentation to enable effective health authority interactions and internal governance reviews.
• Assess CMC change controls to determine regulatory impact, identify filing requirements across regions, evaluate supporting documentation, and elevate risks or gaps as appropriate.
• Track regulatory commitments, health authority questions, and submission-related action items, and coordinate cross-functional responses within agreed timelines.
• Maintain current knowledge of relevant CMC regulations, guidance, and regional expectations, and communicate executional impact to internal stakeholders.
• Contribute to continuous improvement of regulatory processes, templates, SOPs, and systems that support efficient and compliant document development and submission execution.

Qualifications and Skills

• A minimum of a B.S. degree in a scientific or life sciences discipline with a minimum of 10 years experience in Regulatory CMC, manufacturing, analytical development, quality, or related pharmaceutical development environments.
• Demonstrated experience supporting regulatory programs for products intended to treat rare diseases and/or conditions with high unmet medical need is preferred.
• Experience preparing CMC documentation to support clinical trial applications, marketing applications, post-approval submissions, and health authority responses.
• Experience with peptides and injectable dosage forms and/or injection drug delivery devices is required.
• Strong execution skills with demonstrated ability to manage multiple deliverables, coordinate cross-functional input, and deliver high-quality work within aggressive timelines.
• Working knowledge of global CMC regulatory requirements, guidelines, and expectations across development, registration, and lifecycle management in multiple ICH regions.
• Ability to work independently within established strategic direction, identify issues proactively, and elevate risks appropriately.
• Strong organizational, planning, communication, and collaboration skills, with the ability to work effectively across Global Regulatory Affairs, Technical Operations, Quality, and external partners.

This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs. This role may involvesome travel.

The expected salary range for this position is $182,000 - $275,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units.

More about Rhythm

We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.

Core Values

• We are committed to advancing scientific understanding to improve patients’ lives
• We are inspired to tackle tough challenges and have the courage to ask bold questions
• We are eager to learn and adapt
• We believe collaboration and ownership are foundational for our success
• We value the unique contribution each individual brings to furthering our mission

Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law.

Headquartered in Boston, Rhythm is proud to have been named one of the Top Places to Work in Massachusetts.