Director of Quality (GLP/GCLP)

EPM Scientific; Cranbury Township (NJ); On-site; USD 150,000 - 200,000; Full time

Job summary

A fast-growing biotech firm in Cranbury, NJ is seeking a Director of Quality Assurance to lead and develop GLP and GcLP quality systems. This role requires 10+ years in QA leadership and expertise in GLP/GcLP within a CRO or bio/pharma environment. The ideal candidate will drive quality initiatives and oversee regulatory inspections to ensure compliance. Competitive salary and full-time position offered.

Qualifications

• Must have hands-on GLP QA experience in a CRO or bio/pharma setting.
• 10+ years of experience in QA leadership.
• Experience in GLP/GcLP and bioanalysis.

Responsibilities

• Drive the development and improvement of GLP and GcLP quality systems.
• Be the face of Quality during client and regulatory inspections.
• Mentor and grow the QA team.

Skills

GLP QA experience

Leadership

Regulatory inspections

Job description

This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$150,000.00/yr - $200,000.00/yr

Direct message the job poster from EPM Scientific

Life Sciences Senior Recruitment Consultant

A rapidly growing bioanalytical CRO to support their search for a Director of Quality Assurance. This is a leadership role where you'll drive the development and continuous improvement of GLP and GcLP quality systems supporting both nonclinical and clinical testing. You'll be the face of Quality during client and regulatory inspections, help shape regulatory strategy across sites, and build a culture of excellence by mentoring and growing the QA team. This is a great fit for someone with experience in GLP/GcLP - Bioanalysis and 10+ years of QA leadership experience in a CRO or biotech setting.

Qualifications:

• In person job in GLP bioanalytical lab in Pleasanton, CA.
• The position reports directly to the CSO & CEO and is a key leadership role responsible for building and leading the QA function on site.
• Must have hands-on GLP QA experience in a CRO or bio/pharma setting
• Experience in GLP/GcLP, Bioanalysis.
• 10+ years of relevant QA or regulatory background
• Experience leading regulatory and client inspections
• Will oversee quality systems, SOPs, and compliance

If you believe you'd be a good fit for the opportunity and have extensive experience with GLP in a bioanalytical lab or CRO setting, please apply.

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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