In-House Counsel / Regulatory (Life Sciences)

New England Legal Search

Minneapolis (MN)

Hybrid

USD 150,000 - 230,000

Full time

14 days+

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Job summary

New England Legal Search seeks an experienced Regulatory Counsel in the life sciences space to advise on regulatory and quality matters across the product life cycle.

The role emphasizes leading global regulatory strategy, audits, and cross-functional collaboration to drive compliant innovation in data-driven healthcare solutions. This is a hybrid position with opportunities across multiple locations.

Qualifications

  • 8+ years of experience as regulatory counsel in the medical device field.
  • Experience advising on regulatory strategy and global standards.
  • Experience guiding audits and inspections and leading teams through regulatory processes.
  • Ability to collaborate with cross-functional teams to enable compliant product development.

Responsibilities

  • Provide regulatory and quality compliance guidance across the product life cycle.
  • Lead regulatory strategy, submissions, and clearance/approval efforts for devices.
  • Collaborate with R&D, quality, and operations to mitigate risk and ensure compliance.

Skills

Regulatory Counsel
Regulatory Strategy
Audits & Inspections
Life Sciences

Job description

In-House Counsel / Regulatory (Life Sciences)

Title: In-House Counsel / Regulatory (Life Sciences)


Category: Jobs


Organiser: New England Legal Search


Description: A prominent Massachusetts-based medical device leader is seeking a Regulatory Counsel to provide legal advice on regulatory and quality matters. The role involves managing compliance with international regulations, risk management, and process development across the product life cycle. The successful candidate will partner with cross-functional teams to ensure compliance, mitigate risk, and enable innovation in data-driven healthcare solutions. This is a hybrid role offering a significant opportunity to lead regulatory efforts for an industry leader.


Eligibility: Candidates must have 8+ years of experience as regulatory counsel in the medical device field, with expertise in advising on regulatory strategy, supporting audits and inspections, and guiding teams through global standards.


Location: Minneapolis, MN (Multiple locations including MA, CA, FL, IN, and TX)


Fees: None

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