Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Executive – Quality Control (Qc)

Piramal Pharma
3-6 years
preferred by company
Pithampur, India
2 May 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, 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

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 | Analytical Testing | GMP | CDMO | Life Sciences
Experience Required: 3–6 Years (Freshers Not Eligible)
Job Requisition ID: R00001877
Application Deadline: 22 May 2026

About the Company

Piramal Pharma Solutions is a globally recognized Contract Development and Manufacturing Organization (CDMO) providing integrated pharmaceutical development and manufacturing services across the entire drug lifecycle. The company serves global pharmaceutical innovator and generic organizations through its extensive presence across North America, Europe, and Asia.

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

Job Overview

Piramal Pharma Solutions is seeking an experienced Senior Executive – Quality Control (QC) for its Pithampur manufacturing facility. This opportunity is ideal for pharmaceutical quality professionals with hands-on experience in stability analysis, finished product testing, HPLC operations, dissolution testing, GMP laboratory compliance, quality documentation, and pharmaceutical analytical testing.

The selected professional will support critical QC operations involving product quality testing, stability program execution, analytical documentation, data integrity compliance, and regulatory laboratory quality systems.

This role is ideal for candidates seeking growth in pharmaceutical quality control, GMP-regulated analytical laboratories, finished dosage testing, and compliance-focused manufacturing environments.

Key Responsibilities

Quality Control Testing & Product Analysis

  • Perform analysis of:
    • Stability samples
    • Finished pharmaceutical products
    • Routine QC analytical samples
  • Conduct physical and chemical analytical testing as per approved cGMP procedures.
  • Ensure timely execution of quality control activities aligned with product release and stability requirements.

Analytical Instrument Handling

Operate approved analytical methods using:

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

Key responsibilities include:

  • Executing approved analytical methods only
  • Ensuring compliance with validated method configurations
  • Maintaining instrument operational integrity and usage compliance

Stability Program Management

  • Maintain stability incubators and environmental chambers.
  • Prepare monthly stability testing planners.
  • Support ongoing stability study execution and compliance monitoring.
  • Manage testing schedules for stability sample evaluation.

Documentation & Data Integrity Compliance

Maintain accurate and audit-ready documentation including:

  • Laboratory notebooks
  • Certificates of Analysis (COA)
  • Stability Study Reports (SSR)
  • Raw analytical data
  • Instrument usage logbooks
  • QC analytical records

Additional responsibilities:

  • Ensure real-time documentation practices
  • Perform online data entries accurately
  • Support site Data Integrity Compliance Officer (DICO) initiatives
  • Promote data integrity awareness and compliance implementation

Deviation, OOS & Quality Incident Management

  • Immediately report:
    • Deviations
    • Incidents
    • OOT (Out of Trend) observations
    • OOS (Out of Specification) results
  • Support investigation workflows and compliance escalation processes.
  • Ensure timely communication with QC leadership.

Sample Handling & Laboratory Operations

  • Manage sample receipt, inward processing, labeling, storage, and traceability.
  • Maintain chemical inventory records and bin card documentation.
  • Support laboratory housekeeping, audit readiness, and GLP/GMP compliance.
  • Perform additional departmental responsibilities as assigned by QC leadership.

Educational Qualification

Preferred qualifications:

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

Experience Requirements

  • 3–6 years of pharmaceutical Quality Control experience
  • Experience in finished dosage analytical testing or GMP-regulated QC laboratories preferred
  • Hands-on experience with analytical instruments is mandatory