Senior Manager, Regulatory Affairs

Vericel Corporation; Burlington (MA); On-site; USD 188,000 - 205,000; Full time

Job summary

Vericel Corporation in Burlington, MA is seeking a Senior Manager, Regulatory Affairs to oversee regulatory submissions and strategy across biologics and combination products. The role requires leadership across cross-functional teams and independent management of complex regulatory programs.

You will drive IND/BLA submissions, guide regulatory strategy, and ensure alignment with FDA and global requirements, shaping a growing portfolio in cell therapies.

Qualifications

• 8+ years of progressive Regulatory Affairs experience in biotechnology or pharmaceutical industries, including substantial biologics work.
• Experience independently leading complex regulatory projects and cross-functional submissions with limited oversight.
• Ability to adapt to changing regulatory priorities and ensure compliance and deliverable quality.
• Experience with combination products and/or botanicals is a plus.
• Experience with BLA submissions and accompanying amendments/supplements.

Responsibilities

• Plan, prioritize, and manage regulatory activities across development and commercial products.
• Lead assembly and timely submission of INDs, BLAs, and other regulatory dossiers.
• Assess priorities, identify risks, and provide regulatory guidance with proposed solutions.
• Respond to health authority requests and changing regulatory requirements.
• Represent the company with FDA and other regulatory authorities; provide cross-functional leadership on regulatory matters.

Skills

Regulatory strategy

Regulatory submissions

FDA interactions

Regulatory writing

Cross-functional leadership

Biologics experience

Education

Bachelor of Science in a scientific discipline

Advanced degree (preferred)

Job description

Senior Manager, Regulatory Affairs

Regular Full-Time Burlington, MA, US

Senior Manager, Regulatory Affairs

At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care).

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 elevate 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.