CareerPlan

Senior Associate Quality Control - Days

US - Rhode Island - West GreenwichFull-time$79k2026-10-27 → 2026-11-10
No visa sponsorship

Core

Perform raw material testing using sophisticated instrumentation (HPLC, GC, GC-MS), manage sample/data, and ensure alignment with cGMP practices in a biotech manufacturing environment.

Role type

Senior Associate Quality Control (Analytical Testing)

Builds

Raw material testing data and quality documentation for biopharmaceutical products

Domain

Biotechnology / Pharmaceutical Manufacturing

Required skills

HPLC, GC, GC-MS operation, cGMP compliance, laboratory data analysis, equipment maintenance, regulatory documentation, deviation/CAPA review

Preferred skills

ICP-MS, pipetting small volumes, GxP laboratory experience, auditing/defending processes, LEAN principles, project leadership, operational excellence

Technologies

HPLC, GC, GC-MS, ICP-MS, electronic laboratory systems

Responsibilities

Perform testing methods including HPLC, GC and GC-MS; Operate and maintain specialized laboratory equipment; Generate accurate laboratory documentation; Participate in laboratory investigations, inspections and audits; Review and approve procedures, assays, documents and records; Alert management of quality, compliance, supply and safety risks; Support training of new staff

Seniority

Senior, hands-on IC