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Executive – Quality Control (Icp-Ms / Lc-Ms Analyst)

Piramal Pharma
5-8 years
preferred by company
Digwal, Telangana, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L.

Executive – Quality Control (ICP-MS / LC-MS Analyst)

Company: Piramal Pharma Solutions
Location: Digwal, Telangana, India
Job Type: Full-Time
Work Mode: Onsite
Industry: Pharmaceutical | Quality Control | Analytical Chemistry | API Manufacturing | CDMO | Life Sciences
Experience Required: 5–8 Years (Freshers Not Eligible)
Mandatory Experience: Minimum 5 Years in ICP-MS / Advanced Instrumentation Analysis
Job Requisition ID: R00001329
Application Deadline: 20 May 2026

About the Company

Piramal Pharma Solutions is a globally trusted Contract Development and Manufacturing Organization (CDMO) offering end-to-end pharmaceutical development and manufacturing solutions across the entire drug lifecycle. With operations across North America, Europe, and Asia, the company supports global pharmaceutical innovator and generic businesses with advanced API manufacturing, pharmaceutical development, clinical trial supplies, and specialized drug development services.

Job Overview

Piramal Pharma Solutions is hiring an experienced Executive – Quality Control for its Digwal, Telangana facility. This role is ideal for pharmaceutical analytical professionals with deep expertise in ICP-MS, LC-MS, analytical method development, method validation, method transfer, quality control operations, batch release, data integrity, and regulated laboratory compliance.

The ideal candidate will be responsible for advanced analytical testing, instrumentation management, QC documentation review, regulatory compliance, CAPA investigations, analytical release activities, and cross-functional coordination to support production dispatch timelines.

This opportunity is best suited for professionals seeking growth in pharmaceutical quality control, analytical instrumentation, API quality systems, and GMP-regulated manufacturing environments.

Key Responsibilities

Analytical Testing & Quality Control Operations

  • Perform chemical and instrumentation analysis for:
    • In-process samples
    • Raw materials
    • Packing materials
    • Intermediates
    • Finished products
  • Ensure timely analysis and release support aligned with production dispatch schedules.
  • Support production through accurate and timely QC testing execution.

Advanced Instrumentation Analysis

Operate and manage advanced analytical instruments including:

  • ICP-MS (Inductively Coupled Plasma Mass Spectrometry)
  • LC-MS / LC-MS/MS
  • Other pharmaceutical analytical instruments as required

Key responsibilities include:

  • Routine analysis execution
  • Instrument calibration and performance monitoring
  • Instrument qualification compliance
  • Breakdown reduction and maintenance coordination
  • Critical spare inventory management

Method Development, Validation & Transfer

  • Perform and review:
    • Analytical method development
    • Method validation
    • Method verification
    • Analytical method transfer
  • Prepare and review protocols, reports, worksheets, and validation documentation.
  • Support analytical lifecycle compliance aligned with regulatory standards.

Quality Documentation & Data Integrity

  • Maintain online and audit-ready QC documentation including:
    • Calibration records
    • Qualification certificates
    • Standard certificates
    • Traceability records
    • Consumption logs
    • Analytical raw data
    • Method documentation
  • Ensure strong compliance with pharmaceutical Data Integrity expectations.
  • Perform real-time data monitoring and quality record review.

Investigations, CAPA & Compliance Management

  • Lead/support investigations related to:
    • OOS (Out of Specification)
    • OOT (Out of Trend)
    • OOC (Out of Calibration / Control)
    • Deviations
    • Laboratory incidents
  • Implement corrective and preventive actions (CAPA).
  • Reduce repeat analysis and laboratory non-compliance risks.

Batch Release & SAP Operations

  • Review analytical results and release batches within defined timelines.
  • Prepare Certificates of Analysis (COA) as per customer requirements.
  • Approve or reject batches within SAP systems.
  • Support smooth product dispatch operations.

Inventory & Laboratory Resource Management

  • Maintain minimum inventory levels for:
    • Working standards
    • Reference standards
    • Impurity standards
    • Chemicals
    • Reagents
    • Solvents
    • Glassware
    • Instrument spare parts
  • Ensure uninterrupted QC operational readiness.

Team Coordination & Leadership

  • Allocate work to chemists within the QC section.
  • Provide GLP/GMP training to employees, contract staff, and laboratory helpers.
  • Train staff on:
    • Glassware cleaning
    • Safety compliance
    • Good laboratory practices
    • Analytical process discipline

Cross-Functional Coordination

Coordinate effectively with:

  • Quality Assurance (QA)
  • Production
  • PPIC
  • Warehouse
  • TSD
  • External analytical laboratories

Support seamless batch release, dispatch execution, and issue resolution.

Safety, Housekeeping & Compliance

  • Ensure safe laboratory working practices.
  • Maintain clean environmental conditions and instrument housekeeping.
  • Promote use of required safety appliances.
  • Support SFTI and workplace compliance initiatives.

Educational Qualification

Preferred qualifications:

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

Experience Requirements

  • Minimum 5 years of pharmaceutical Quality Control experience
  • Mandatory expertise in ICP-MS analysis
  • Experience with LC-MS / LC-MS/MS
  • Experience in GMP-regulated analytical laboratories
  • Exposure to API or pharmaceutical manufacturing quality environments preferred