Regulatory Affairs Manager (ADX-310-20)

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Regulatory Affairs Manager (ADX-310-20)

 

COMPANY SUMMARY:

 

In October 2020, Invitae Corporation (NYSE: NVTA) combined with ArcherDX, a genomic analysis company specializing in cancer diagnostics and monitoring, to create a leading comprehensive medical and cancer genetics company. As a combined company, Invitae, is bringing world-class genetic testing and diagnostics into mainstream medicine to improve healthcare for billions of people. Our goal is to aggregate the world’s genetic tests into a single service with higher quality and accuracy, faster turnaround time and actionable results. Learn more at invitae.com and archerdx.com.

POSITION SUMMARY:

The Regulatory Affairs Manager will be responsible for representing the regulatory function on teams working on the development of in vitro diagnostic medical devices for global regulatory submissions. This position will lead, mentor and develop a team within Archer’s primary class of trade.
RESPONSIBILITIES:

  • Represent regulatory on the program core team, which handles escalation from project teams on issues of study design, timeline changes and resource constraints.
  • Develop, mentor, and coach a productive and efficient regulatory team.
  • Demonstrate accountability for all program goals, timelines, and compliance decisions to functional management.
  • With your team’s support, develop a cohesive and detailed regulatory strategy for meeting Archer’s goal to commercialize an industry leading companion diagnostic IVD platform.
  • Provide input on IVD development and clinical trial questions to promote compliance and fidelity to health authority guidance, regulations and feedback.
  • Request and drive quality feedback from health authorities in the form of pre-submission meetings.
  • Promote consistency in regulatory department feedback in a cross-functional environment through high-quality training and team communication.
  • Speak for the Archer regulatory team to external partners, such as pharmaceutical co-development partners.
  • Support the Quality group with input the quality management system and strong ownership of regulatory processes.
  • Perform other duties as assigned by supervisor, including case-by-case general compliance matters.

 

EXPERIENCE:

  • Five or more years experience in regulatory affairs, including primary submission ownership.
  • One or more years experience managing a regulatory team.
  • High degree of proficiency with MS Office and Adobe PDF creation
  • Familiarity medical device and/or IVD design control processes
  • Experience with good manufacturing practice and good document practice.
  • Experience with quality systems in regulated space preferred, with responsibility for generating new documents and conducting team reviews.
  • Fine research skills with a knack for sketching out solutions to novel issues.
  • Ability to interact with multiple disciplines, and communicate clearly and effectively verbally and in writing.
  • Ability to work independently, and report progress efficiently.
  • Ability to multitask and work within a fast-paced dynamic team environment

EDUCATION:

  • Minimum B.S./B.A, preferably in a technical field.
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Location

Conveniently located minutes from downtown Boulder via Pearl Street or the Goose Creek Path. Easily commutable from all directions.

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