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About the job

Why Sarepta? Why Now?

Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne Muscular Dystrophy and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. Our next-generation siRNA platform is focused on chronically administered therapies for neurodegenerative and pulmonary diseases.

We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.

What Sarepta Offers

At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:

Physical and Emotional Wellness

Financial Wellness

Support for Caregivers

For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us

The Importance of the Role Lead or co-lead for one RA CMC development and/or marketed product and provide support for Chemistry, Manufacturing and Controls (CMC) Regulatory Affairs. Works closely with subject matter experts within CMC technical operations and QA working within a CMC sub-team structure and serving as a member of the GRT. Contributes to the development of fit for purpose high quality documentation (e.g., INDs, CTAs, NDAs, reports, and correspondences) to support global Health Authority interactions. May oversee activities of junior regulatory personnel. Builds/maintains relationships globally and cross-functionally to ensure effective communication & efficient implementation of regulatory activities for assigned programs. Applies and further develops knowledge of assigned market regulatory procedures.

The Opportunity to Make a Difference

Contributes to developing CMC regulatory strategies for assigned projects and programs while accurately interpreting and reflecting regulatory guidelines and corporate guidelines

Coordinates the preparation and submission of documents to appropriate regulatory agencies for assigned projects and programs to implement regulatory strategy in line with corporate goals Responsible for completing change control regulatory assessments, maintenance of regulatory tracker and submission preparation activities.

May lead CMC submissions and agency responses.

Ensure documentation management and record keeping are compliant with regulatory expectations and Sarepta SOPs.

Required to support preparation for inspection readiness

Maintains/further develops knowledge of relevant evolving regulation and guidance

Global Regulatory Teams –contributor to establish and implement regulatory strategy

Impact and Scope:

Works on issues where analysis of situations or data requires a knowledge of organizational objectives and current business trends

Establishes and assures adherence to budgets, schedules, work plans, and performance requirements

Works on objectives that have major impact on functional area and the organization

Erroneous decisions may result in critical delay(s) in schedules and/or unit operations and may jeopardize overall business activities.

More about You

Experience working in GRTs and cross functional teams

Knowledge of drug development, ICH guidelines and regulatory process.

Experience of IND/CTA, IMPDs, Orphan drug designation, Agency Advice, NDA and/or MAA submission

Demonstrated experience with and a clear understanding of submission content and format requirements

Ability to successfully manage projects/timelines, organize/track complex information & prioritize, by communicating with internal and external stakeholders

Adaptive communication skills (including interpersonal, written, verbal) and able to influence others without authority

Solid sense of accountability and sound judgement; highest ethical standards and focus on quality and details

Ability to evaluate and recommend process improvement and suggest/implement best practices.

RAC certification recommended

Proficiency with Microsoft Office Applications; Word, Excel, Outlook, Adobe, and regulatory/quality systems.

BS or equivalent, 8+ years relevant experience

What Now?

We’re always looking for solution-oriented, critical thinkers.

So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.

#LI-Hybrid

#LI-CM1

This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.