Senior Manager, Regulatory Affairs

Vericel Corporation; New Jersey; Hybrid; USD 188,000 - 205,000; Full time

Job summary

Vericel Corporation is seeking a Senior Manager, Regulatory Affairs to independently manage complex regulatory projects and submissions across biologics. You will develop strategies, lead cross‑functional teams, and serve as regulatory lead on initiatives, ensuring timely approvals and compliance.

The role requires strong regulatory writing, knowledge of eCTD, and experience with BLA submissions, with on-site work in Burlington, MA and potential remote Fridays.

Qualifications

• 8+ years of progressive Regulatory Affairs experience in biotech/pharma with biologics.
• Experience leading complex regulatory projects with limited supervision.
• Ability to adapt to changing regulatory priorities and act with urgency.

Responsibilities

• Plan, coordinate, and execute regulatory submissions across products.
• Develop regulatory strategies to support timely approvals and compliance.
• Lead cross-functional teams and provide regulatory guidance to management.
• Interact with FDA and other authorities; manage dossiers and amendments.
• Maintain current regulatory knowledge and drive process improvements.
• Travel up to a few times per year as required.

Skills

Regulatory leadership

Biologics

FDA interactions

BLA submissions

Regulatory strategy

Cross-functional collaboration

FDA/health authority knowledge

eCTD knowledge

Education

Bachelor of Science in a scientific discipline

Advanced degree (preferred)

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Senior Manager, Regulatory Affairs

Regular Full-Time Burlington, MA, US

4 days ago Requisition ID: 1364

Senior Manager, Regulatory Affairs

Position Summary

Reporting to the Director, Regulatory Affairs, the Senior Manager, Regulatory Affairs independently manages, evaluates, and completes complex regulatory projects consistent with company goals. The position is responsible for the timely planning, coordination, and execution of regulatory submissions and for providing clear, practical regulatory strategy and guidance to cross-functional teams.

The Senior Manager must work with a high degree of independence, exercise sound judgment, act quickly when regulatory or business needs arise, and proactively identify and advance activities without waiting for immediate direction. The role supports a varied portfolio of products and must effectively interpret and apply differing regulatory requirements across product types, development stages, and product lifecycles.

Schedule:

This position is on-site Monday-Thursday at our Burlington, MA office, with the ability to work remotely on Fridays.

Essential Functions:

• With minimal supervision, independently plan, prioritize, and manage regulatory activities across assigned development and commercial products. Develop and implement regulatory strategies that support timely approvals, continued compliance, and company objectives.
• Manage the assembly and timely submission of applications (i.e., INDs, BLAs and other dossiers) as required for investigation and registration of biologics.
• Proactively assess priorities, identify regulatory risks and opportunities, make timely recommendations, and escalate significant issues with proposed solutions or mitigation plans.
• Respond rapidly and effectively to changing regulatory requirements, health authority requests, emerging product issues, and shifting business priorities while maintaining the quality and compliance of regulatory deliverables.
• Ensure regulatory submissions are maintained in compliance with regulatory requirements.
• Represent the company in its dealings with the FDA and other regulatory authorities, as appropriate.
• Serve as the regulatory lead or subject‑matter expert on cross‑functional project teams and provide timely, decisive guidance across a variety of products, regulatory pathways, and applicable requirements, including biologics and combination products, as assigned.
• Develop and maintain current regulatory knowledge and advise management of significant developments.
• Contribute to internal improvements related to best practices and SOPs.
• Perform other duties as required, interfacing with other departments, CROs, and external vendors as needed

Basic Qualifications:

• 8+ years of progressive Regulatory Affairs experience in the biotechnology or pharmaceutical industry, including substantial experience supporting biologics.
• Demonstrated experience independently leading complex regulatory projects, developing regulatory strategy, and driving cross‑functional submissions through completion with limited oversight.
• Demonstrated ability to rapidly adapt to changing regulatory and business priorities, act with an appropriate sense of urgency, and make timely decisions while maintaining regulatory compliance and deliverable quality.
• Previous experience with combination products and/or botanicals a plus.
• Experience and knowledge in preparation of BLA submissions and supportive amendments and supplements.
• Experience with prescription drug advertising regulations and promotional review committee.
• Experience with labeling regulations.
• Working knowledge of FDA regulations and understanding of FDA structure and function.
• Working knowledge of eCTD elements and structure.
• Strong regulatory writing skills and verbal communication skills.
• Collaborative, solution‑oriented team member with the ability to clearly communicate, negotiate, and influence regulatory strategy and recommendations with cross‑functional partners, senior leadership, external partners, and health authorities.
• Attention to detail and the ability to operate independently, act with urgency, manage multiple competing priorities, and work effectively within multidisciplinary teams and with external partners and vendors.

Education:

• Bachelor of Science in a scientific discipline.
• Advanced degree (preferred)

Working Conditions & Physical Demands:

• Occasional travel (5-10%)

Why Vericel?

Mission-Driven Work: Help bring potentially life-enhancing cell therapies to patients with serious medical conditions.

Innovative Products: Work with a first‑in‑class therapy backed by clinical success and provider trust.

Career Growth: Be a part of a growing organization with opportunities to expand your impact.

Collaborative Culture: Join a supportive, cross‑functional team that values passion, integrity, and excellence.

The salary range Vericel reasonably and in good faith expects to pay for this position at the time of this posting is $188,000 - $205,000 annually.

The actual salary offered will be determined based on factors such as the candidate’s qualifications, experience, and skills. Bonus, incentive pay, equity and benefits may be provided in addition to the base compensation listed above.

In accordance with Massachusetts law, Vericel provides the pay range that it reasonably and in good faith expects to pay for a particular and specific employment position at the time of posting or offer. This range is subject to change based on business needs, market conditions, and individual qualifications. Employees and applicants may request the pay range for their position or for a position to which they are applying. Retaliation for making such a request is strictly prohibited.

EEO Statement

All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer.

Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.