GMP QA Manager - Analytical Lab Leader (On-Site)

Pacelabs

Lebanon, Northern (NJ, KY)

Hybrid

USD 115,000 - 125,000

Full time

14 days+
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Benefits offered by this job

Competitive salary and annual bonus
401(k) with company match
Medical, dental, and vision benefits
Paid time off and holidays
Tuition reimbursement and EAP

Job summary

Pace Life Sciences in Lebanon, NJ is hiring a Quality Manager to oversee the Quality Management System (QMS) and ensure compliance with FDA, ICH, USP, ISO and cGMP. This full-time role supports analytical testing operations, audits, investigations, and continuous improvement.

The ideal candidate has a chemistry/biological background, 7+ years QA experience, 3+ years of leadership, and strong communication. Responsibilities include document control, deviations, CAPAs, change controls, data

Qualifications

  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field.
  • 7+ years of QA experience in pharmaceutical/biotech/CDMO or contract lab.
  • 3+ years of leadership or people management experience.
  • Strong knowledge of FDA regulations, cGMP, ICH guidelines, and data integrity.

Responsibilities

  • Oversee and maintain the Quality Management System (QMS).
  • Provide QA oversight of analytical lab operations and GMP testing.
  • Review documentation, protocols, reports, investigations, and records.
  • Lead audits, inspections, and client/regulatory activities.
  • Drive continuous improvement and data integrity practices.

Skills

Quality Assurance
Leadership
FDA regulations
cGMP
ICH guidelines
Data integrity
Documentation and reporting

Education

Bachelor's in Chemistry/Biology/Pharmaceutical Sciences
Advanced degree preferred

Job description

Pace Life Sciences in Lebanon, NJ is hiring a Quality Manager to oversee the Quality Management System (QMS) and ensure compliance with FDA, ICH, USP, ISO and cGMP. This full-time role supports analytical testing operations, audits, investigations, and continuous improvement.

The ideal candidate has a chemistry/biological background, 7+ years QA experience, 3+ years of leadership, and strong communication. Responsibilities include document control, deviations, CAPAs, change controls, data

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