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QC Analytical - Group Leader

Sanford, NC, us💼 Full-time🗓 2026-09-29 → 2026-09-30

Core

Lead a team in performing routine and non-routine analytical testing of pharmaceutical products, raw materials, and process samples within a GMP-regulated laboratory.

Role type

Senior IC QC Analytical Group Leader

Builds

GMP-compliant test records, validation protocols, and stability reports for pharmaceutical products

Domain

Pharmaceutical manufacturing / Quality Control

Required skills

GMP compliance, analytical testing (UV-VIS, HPLC, UPLC, pH, osmolality, TOC, conductivity), instrument operation, GMP documentation creation and review, complex data analysis, accurate pipetting, team coaching, workflow planning

Preferred skills

Previous leadership experience, experience with analytical standards and reagents

Technologies

HPLC, UPLC, UV-VIS, pH meters, conductivity meters, Solo VPE, Osmometers, TOC analyzers

Responsibilities

Perform routine and non-routine analytical testing; create, review, and approve GMP documentation; act as a technical resource and trainer; coach and develop direct reports; plan and monitor workflows; recommend operational improvements

Seniority

Senior, hands-on IC with leadership responsibilities

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