Senior Executive - QA (QMS)

Darwinbox Digital Solutions Pvt. Ltd.

Solan

On-site

INR 1,500,000 - 2,100,000

Full time

6 hours ago
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Job summary

Darwinbox Digital Solutions Pvt. Ltd. is seeking a senior QA/QMS professional for a manufacturing unit in pharma. The role requires handling CAPA, investigations, change controls, and risk management, with responsibility for SOP review and training of staff.

Location: Baddi, Himachal Pradesh. The position is permanent/full-time with extensive regulatory and quality assurance duties. Candidates should have 8-9 years of related experience and be prepared to lead cross-functional quality

Qualifications

  • Responsible for handling and review of Quality Management System including Change controls, Deviations, investigation and Corrective and Preventive Action.
  • Preparation of CAPA, tracking of CAPA response and implementation and CAPA closure.
  • Handling of product complaints and ensuring the investigations and closure.
  • Tracking and Handling of Quality Risk Management.
  • Review of Standard Operating Procedures and their compliance.
  • To impart training to departmental personnel on own departmental SOPs and cross functional SOPs.
  • Updation of Site Master File.
  • Preparation of Monthly and Quarterly Review for Management Review.

Responsibilities

  • Handle and review Quality Management System processes (Change controls, Deviations, investigations).
  • Prepare and track CAPA, ensure timely closure.
  • Investigate product complaints and close investigations.
  • Monitor Quality Risk Management activities.
  • Review SOPs for compliance and effectiveness.
  • Train staff on SOPs and cross-functional SOPs.
  • Maintain Site Master File updates.
  • Generate Monthly/Quarterly Management Reviews.
  • Perform other duties as assigned by Head of Department.

Skills

Quality Management
CAPA Management
Investigations
Risk Management
SOP Compliance

Job description

MANUFACTURING UNIT (PHARMA), Baddi, Himachal Pradesh, India

8 - 9 Years

PERMANENT

Job Description
  • Responsible for handling and review of Quality Management system including Change controls, Deviations,investigation and Corrective and Preventive Action.
  • Preparation of CAPA, tracking of CAPA response and implementation and CAPA closure.
  • Handling of product complaints and ensuring the investigations and closure.
  • Tracking and Handling of Quality Risk Management.
  • Review of Standard Operating Procedure and its compliance.
  • To impart training to departmental personnel on own departmental SOPs and cross functional SOPs.
  • Updation of Site Master File.
  • Preparation of Monthly and Quarterly Review for Management Review.
  • To perform any other works as and when assigned by Head of department.
Job Snapshot
Updated Date

21-09-2026

Job ID

JOB_1382

ONCOLOGY FORMULATION PLANT
Location

Location MANUFACTURING UNIT (PHARMA), Baddi, Himachal Pradesh, India

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