Quality Supervisor

JCW Group

Denver (CO)

On-site

USD 120,000 - 150,000

Full time

9 days ago
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Job summary

JCW Group is seeking a Quality Compliance Team Lead for our Colorado site to manage audit and inspection programs and keep the organization audit-ready year-round.

You will lead a team of 4 (mix of onsite and remote) and collaborate with cross-functional departments to drive regulatory compliance, risk mitigation, and continuous improvement.

Open to relocation and this on-site role demands strong presentation skills plus the ability to coach performance conversations across the organization.

Qualifications

  • 8+ years in Quality/Compliance within pharma or medical devices.
  • 5+ years managing audits/inspections (regulatory and internal).
  • 3+ years leading quality systems elements — deviations, internal audits, training, PQRs.
  • Experience coaching performance and handling conversations with team members and leaders.
  • Bachelor’s in a scientific/technical field; relevant quality certifications a plus.

Responsibilities

  • Lead audit and inspection programs across the site.
  • Coordinate regulator inspections and host visits.
  • Ensure audit readiness and regulatory compliance year-round.
  • Manage a team of 4 (onsite and remote) and collaborate with cross-functional departments.

Skills

Quality Compliance
Audit Management
Regulatory Inspections
Leadership
Risk Communication

Education

Bachelor's degree in science/technical field

Job description

Quality Compliance Team Lead | Colorado (On-Site)

Our client, a growing pharmaceutical manufacturer in Colorado, is hiring a Quality Compliance Team Lead to manage audit and inspection programs across the site.

You’ll be the point person when regulators show up — managing the logistics of hosting inspections, keeping the organization audit-ready year-round, and leading a team of 4 (mix of onsite and remote) while working closely with departments across the site.

What we’re looking for:

  • 8+ years in Quality/Compliance within pharma (open to strong medical device backgrounds)
  • 5+ years managing audits/inspections (regulatory and internal)
  • 3+ years leading quality systems elements — deviations, internal audits, training, product quality reviews
  • Experience managing people through performance conversations, not just assigning tasks — this team is tenured and has strong personalities
  • Comfortable presenting to leadership and communicating compliance risk clearly, up and down the org
  • Bachelor’s in a scientific/technical field; relevant quality certifications a plus

This is a growth seat — ideal for someone who wants to build toward a broader leadership track.

On-site 5 days/week. Open to candidates outside Colorado willing to relocate.

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