CareerPlan
This role has closed. Browse similar live roles below, or see all open jobs →

Quality Assurance Associate - Drug Product

Hyderabad, TS, inFull-time2026-11-04 → 2026-11-10

Core

Ensure shop floor compliance and monitor GMP adherence for Formulation, Filling, Optical Inspections, and Packaging Activities in a biosimilar manufacturing facility.

Role type

Quality Assurance Associate (Drug Product)

Builds

Commercial and developmental biosimilar drug products

Domain

Pharmaceutical manufacturing (Biosimilars)

Required skills

GMP compliance, Line Clearance, Aseptic Media Fill Simulation, ALCOA principle verification, Change Control review, Deviation investigation, CAPA execution, Audit participation, APQR compilation, OOS/OOL investigation, Equipment audit, Transport validation, Temperature data verification

Preferred skills

Experience in Injectable products, Knowledge of cGMP facilities

Technologies

Manufacturing execution systems, GMP record systems, Validation protocols

Responsibilities

Ensure shop floor compliance by involving in Line Clearance activities for Formulation, Filling, Optical Inspections and Packaging Activities; Monitor and ensure that all activities involved in Formulation, Filling, Optical Inspections and Packaging Activities are in compliance with GMP and Standard operating procedures; Review of Aseptic Media Fill Simulation Protocols and Reports; Perform periodic verification of GMP records to ensure that data generated and documented at GMP floor are in compliance with ALCOA principle; Review and Approval of MFRs, BOMs, BPRs, SOPs and Validation protocols related to Formulation, Filling and Packaging Operations; Perform investigation for deviations, and market complaints; Participate External and Internal Audits; Compilation of Annual product quality report (APQRs) for commercial drug products; Sampling of Drug Product samples for LRA testing; Support for out of specification/out of limit (OOS/OOL) investigations related to product and environments; Perform System / Process, audit trial for manufacturing equipment; Support, monitor Transport Validation activities; Verify temperature data of export shipments.

Seniority

Mid-Senior level (8-10 years experience)