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Visakhapatnam, in💼 Full-time🗓 2026-09-23 → 2026-09-25

Core

Execute analytical testing, stability protocols, and quality compliance procedures for pharmaceutical raw materials, intermediates, and finished products.

Role type

Senior QC Analyst / Quality Control Team Member

Builds

Quality data, stability reports, and compliance documentation for pharmaceutical manufacturing

Domain

Pharmaceutical manufacturing / Quality Control

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

HPLC operation, stability testing, GMP/GLP/GDP compliance, OOS/OOT investigation, CAPA management, COA preparation, instrument calibration, sampling procedures

Preferred skills

Method transfer experience, regulatory submission support, isolator handling, LMS training completion

Technologies

HPLC, LMS, stability chambers

Responsibilities

Perform analytical tests per specifications, prepare and review QC protocols, handle stability chamber operations and data reporting, investigate OOS/OOT incidents, manage CAPA closure, prepare Certificates of Analysis (COA), ensure GMP/GLP compliance, operate lab instruments per SOPs.

Seniority

Senior, hands-on IC

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