Manager, Regulatory Affairs

Foundation Medicine, Inc.; Boston (MA); Hybrid; USD 80,000 - 120,000; Full time

Job summary

An established industry player is seeking a Regulatory Affairs Manager to lead the regulatory strategy for innovative cancer diagnostic products. This role involves managing regulatory submissions, developing strategies for product development, and ensuring compliance with FDA regulations. The ideal candidate will have a strong background in life sciences and regulatory affairs, with a passion for improving patient outcomes through advanced genomic technologies. Join a team dedicated to transforming cancer care and making a real impact in the lives of patients.

Benefits

Health Insurance

401(k) Plan

Flexible Working Hours

Professional Development Opportunities

Paid Time Off

Work from Home Options

Employee Assistance Program

Qualifications

• 5+ years of experience in life sciences or regulatory affairs.
• Strong understanding of FDA guidance and regulations.
• Experience with genomic data analysis in a regulated environment.

Responsibilities

• Manage pre-market submissions for regulatory approval.
• Develop regulatory strategy for complex projects.
• Interface with regulatory authorities on technical matters.

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 Degree in Science

Tools

Regulatory Submission Documentation

Technical Document Review

Job description

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 cross functional 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.

#LI-Hybrid

About Us

Foundation Medicine, Inc. (FMI) began with an idea - to simplify the complex nature of cancer genomics, bringing cutting-edge science and technology to everyday cancer care. Our approach generates insights that help doctors match patients to more treatment options and helps accelerate the development of new therapies. Foundation Medicine is the culmination of talented people coming together to realize an important vision, and the work we do every day impacts real lives.

Foundation Medicine is proud to be an Equal Opportunity and Affirmative Action employer and considers all qualified applicants for employment without regard to race, color, religion, sex, gender, sexual orientation, gender identity, ancestry, age, or national origin. Further, qualified applicants will not be discriminated against on the basis of disability or protected veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also FMI's EEO Statement and EEO is the Law and Supplement. If you have a disability or special need that requires accommodation, please let us know by completing this form. (EOE/AAP Employer)