CareerPlan

Team Member - Quality Control

Baddi, HP, inFull-time2026-11-04 → 2026-11-10

Core

Execute analytical testing and quality control activities for in-process and finished pharmaceutical products in a GMP-compliant laboratory environment.

Role type

Quality Control Analyst (Pharmaceuticals)

Builds

Analytical test reports and data for drug manufacturing processes

Domain

Pharmaceuticals / Life Sciences

Required skills

Chromatography (HPLC, GC, FTIR, UV-Vis), Regulatory Compliance (GMP, GLP), Technical Documentation, Change Control, Laboratory Information Management, Risk Management, Product Quality (QA/QC), Current Good Manufacturing Practices (cGMPS), Good Laboratory Practice (GLP), Quality Management Systems (QMS)

Preferred skills

Advanced Instrumentation (LC-MS, ICP-MS, NMR), Biostatistical Analysis (SAS, JMP), OOS Investigation, Method Validation

Technologies

SAP, LIMS, HPLC, GC, FTIR, UV-Vis, LC-MS, ICP-MS, NMR, SAS, JMP

Responsibilities

Calibrate analytical instruments and equipment, perform analysis of in-process and finished product samples, maintain laboratory standards and chemicals, initiate CRN/OOS/incidents, prepare records of analysis and test reports, participate in process and cleaning validations.

Seniority

Mid-level, hands-on IC