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Senior Executive – Quality Control (Qc)

Piramal Pharma
3-6 years
preferred by company
Pithampur, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Senior Executive – Quality Control (QC)

Company: Piramal Pharma Solutions
Location: Pithampur, Madhya Pradesh, India
Job Type: Full-Time
Work Mode: Onsite
Industry: Pharmaceutical | Quality Control | GMP | Analytical Testing | CDMO | Life Sciences
Experience Required: 3–6 Years (Freshers Not Eligible)
Job Requisition ID: R00001878
Application Deadline: 22 May 2026

About the Company

Piramal Pharma Solutions is a globally recognized Contract Development and Manufacturing Organization (CDMO) delivering end-to-end pharmaceutical development and manufacturing solutions across the drug lifecycle. The company supports global innovator and generic pharmaceutical organizations through a strong integrated presence across North America, Europe, and Asia.

Its service portfolio includes drug discovery, pharmaceutical development, API manufacturing, finished dosage formulations, clinical trial supplies, highly potent APIs, and advanced pharmaceutical manufacturing solutions.

Job Overview

Piramal Pharma Solutions is hiring a Senior Executive – Quality Control (QC) for its Pithampur, Madhya Pradesh manufacturing facility. This opportunity is ideal for experienced pharmaceutical quality control professionals with hands-on expertise in finished product analysis, stability testing, HPLC operations, dissolution testing, GMP/GLP compliance, data integrity, and laboratory documentation.

The selected candidate will support quality control laboratory operations, analytical testing of pharmaceutical products, regulatory documentation compliance, sample handling, stability management, and laboratory quality systems.

This role is ideal for professionals seeking career growth in pharmaceutical QC, analytical laboratory operations, GMP-regulated manufacturing, and compliance-driven quality environments.

Key Responsibilities

Pharmaceutical Quality Control Testing

  • Perform analysis of:
    • Stability samples
    • Finished pharmaceutical products
    • Routine QC samples
  • Execute analytical testing in accordance with current Good Manufacturing Practices (cGMP) and approved quality procedures.
  • Perform physical and chemical quality control testing for pharmaceutical products.

Analytical Instrument Operations

Operate and perform testing using:

  • HPLC (High Performance Liquid Chromatography)
  • KF (Karl Fischer) Instrument
  • Dissolution Testing Apparatus
  • UV Spectrophotometer
  • IR Instrument
  • pH Meter
  • Friability Tester
  • Disintegration Test (DT) Equipment

Responsibilities include:

  • Running approved analytical methods
  • Maintaining compliance with validated method configurations
  • Ensuring instrument usage follows approved QC procedures

Stability Management

  • Maintain stability chambers and incubators.
  • Prepare monthly stability planning schedules.
  • Monitor stability sample management and testing timelines.
  • Support product stability compliance activities.

Documentation & Data Integrity Compliance

  • Maintain:
    • Analytical raw data
    • Laboratory notebooks
    • Certificates of Analysis (COA)
    • Stability Study Reports (SSR)
    • Equipment usage logbooks
    • QC records
  • Ensure concurrent documentation and accurate online data entries.
  • Support site Data Integrity Compliance Officer (DICO) initiatives.
  • Maintain strict compliance with pharmaceutical data integrity standards.

Deviation, OOS & Compliance Reporting

  • Immediately report:
    • Deviations
    • Incidents
    • OOT (Out of Trend)
    • OOS (Out of Specification) results
  • Support investigations and corrective action processes.
  • Ensure compliance with GMP, GLP, and quality management systems.

Sample Handling & Laboratory Operations

  • Manage receipt, inward processing, storage, and handling of QC samples.
  • Maintain chemical store bin cards and inventory records.
  • Support laboratory housekeeping, organization, and audit readiness.
  • Perform additional QC responsibilities assigned by department leadership.

Educational Qualification

Preferred qualifications include:

  • B.Pharm / M.Pharm
  • B.Sc / M.Sc in Chemistry
  • Pharmaceutical Chemistry / Analytical Chemistry / Life Sciences

Experience Requirements

  • 3–6 years of pharmaceutical Quality Control laboratory experience
  • Experience in finished dosage QC, analytical testing, or GMP-regulated pharmaceutical manufacturing preferred
  • Hands-on instrument operation experience is mandatory