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The Research and Development team at Foundation Medicine is constantly pushing the envelope to transform cancer care.

Watch the video above to see how each member has the chance to make a real impact. 

 

Manager Regulatory Affairs

  • Towne Centre Ct., San Diego, California, United States
  • Full Time

About the Job

The Manager, Regulatory Affairs 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 4+ years of experience in life sciences, biopharmaceutical, medical device, biologics regulatory or closely related field, OR

• Advanced Degree (Master’s or Doctorate Degree) in science, law, health policy, regulatory affairs or engineering and 2+ years of experience in life sciences, biopharmaceutical, medical device, biologics regulatory or closely related field

• 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

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