Manager, Regulatory Affairs

Foundation Medicine; Boston (MA); Hybrid; USD 80,000 - 140,000; Full time

Job summary

An established industry player is seeking a Regulatory Affairs Manager to lead regulatory strategies and submissions for innovative diagnostic products. This role involves collaborating with cross-functional teams to ensure compliance with FDA regulations and support the development of genomic biomarkers for cancer diagnostics. The ideal candidate will possess a strong background in regulatory affairs, particularly within the life sciences sector, and demonstrate exceptional communication and project management skills. Join a dynamic team committed to advancing patient care through innovation and collaboration.

Qualifications

• 5+ years in regulatory affairs or related field.
• Experience with FDA submissions and regulations.
• Strong communication and problem-solving skills.

Responsibilities

• Manage pre-market submissions for regulatory approval.
• Develop regulatory strategies for product development.
• Interface with FDA and external partners.

Skills

Regulatory Affairs

FDA Regulations

Project Management

Genomic Data Analysis

Communication Skills

Education

Bachelor's Degree in Life Sciences

Master's Degree in Regulatory Affairs

Doctorate in Relevant Field

Job description

About the Job
The Regulatory Affairs Manager is responsible for supporting the regulatory function and its activities, the
development of regulatory strategy, and contributing the regulatory approval process (including US FDA
and other regulatory authorities) for FMI products. The incumbent functions as the regulatory
representative on cross-functional teams as well as prepares and submits packages to the FDA for
approval of new products or new companion diagnostic indications. The position actively supports the
development of regulatory strategy focused on the use of NGS technology for companion diagnostic
assays for cancer patients. Additionally, this position partners closely with product development teams
and external partners focused on development of genomic biomarkers and companion diagnostic
indications.

Key Responsibilities
• Manage pre-market submissions for regulatory approval of in vitro companion diagnostic medical
devices in the US market.
• Develop regulatory strategy with oversight for complex projects, including internal FMI projects as
well as biopharma partner projects.
• Develop and implement regulatory strategy for non-clinical product development and clinical
development.
• Provide regulatory support for currently marketed products, e.g., review engineering changes,
labeling, promotional material, product change control documentation to ensure compliance with
federal regulations and health authority guidance, including for changes requiring regulatory
agency approval or notification, as pertains to US regulatory requirements.
• Represent FMI in interactions with external partners for companion diagnostic development or
support for partner drug filings.
• Review and edit technical documents to be included in submission, which may include validation
protocols and reports and/or other development documentation.
• Author regulatory submission documentation, including SRDs, IDEs, and PMAs.
• Ensure that software and data products are developed and validated to standards required for
FDA-regulated products and/or for data included as part of a drug or diagnostic regulatory
submission (e.g. SRDs, IDEs, Pre-Submissions, PMA).
• Acquire and maintain current knowledge of applicable regulatory requirements, scientific and
technical issues in the discipline as relevant to assigned projects.
• Interpret and apply FDA regulations and guidance documents to business practices, evaluating
risk and proposing solutions to business challenges based on regulatory strategy.
• Interface with regulatory authorities on regulatory and technical matters as directed, including lead
meetings with the regulatory authorities.
• Manage and mentor junior members of the Regulatory Affairs Team.
• Represent Regulatory Affairs department at cross-functional internal project meetings.
• May perform other duties as required or assigned.

Qualifications

Basic Qualifications
• Bachelor’s Degree and 5+ years of experience in life sciences, biopharmaceutical, medical
device, biologics regulatory or closely related field, OR
• Master’s Degree in science, law, health policy, regulatory affairs or engineering and 3+ years of
experience in life sciences, biopharmaceutical, medical device, biologics regulatory or closely
related field, OR
• Doctorate Degree in science, law, health policy, regulatory affairs or engineering
• Experience in regulatory affairs

Preferred Qualifications

• 2+ years of experience in regulatory affairs within the life sciences industry
• Experience:
• interpreting and applying FDA guidance and regulations
• interfacing with the FDA (e.g., CDRH), including submissions (e.g., SRDs, IDEs, PMAs)
and with pre-submission meetings
• preparing and managing IDE and PMA submissions
• with genomic data analysis, especially in a regulated environment
• Industry experience in oncology, NGS, IVD, CDx, CAP/CLIA, and/or regulatory
• Understanding of the principles of scientific, engineering, physiology and medical device use
• History of effective time management, organization, prioritization and multitasking
• History of proactive and independent problem solving
• Strong collaborative skill set, demonstrated by creative and effective contributions in crossfunctional or cross-departmental partnerships
• Demonstrated organization, attention to detail and high level of accuracy
• Effective and clear oral and written communication skills, and negotiation skills
• Demonstrated ability to:
• prepare and present information to groups
• interact effectively across relevant functions
• manage multiple activities or projects
• work in a fast-paced/entrepreneurial environment
• Understanding of HIPAA and the importance of patient data privacy
• Commitment to reflect FMI’s values: Patients, Passion, Innovation, and Collaboration.

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