Senior Executive - QA (Validation)

Darwinbox Digital Solutions Pvt. Ltd.; Solan; On-site; INR 600,000 - 900,000; Full time

Job summary

Darwinbox Digital Solutions Pvt. Ltd. seeks a skilled Validation/Qualification professional for its Pharma manufacturing unit in Baddi, Himachal Pradesh. The role focuses on preparation/review of validation protocols, annual planning, and adherence to QA standards.

The incumbent will execute qualification activities at the department level, investigate deviations, and ensure proper documentation and equipment validation status across QC and production lines.

Qualifications

• Experience in preparing and reviewing validation/qualification SOPs.
• Experience in executing qualification activities at department level.
• Familiarity with QA documentation and deviation investigation.

Responsibilities

• Prepare and review Validation/Qualification protocols and reports.
• Execute and verify Qualification activities at department level.
• Investigate non-conformance/deviations in validation activities.
• Maintain Validation Master Plan and track updates.
• Assign Equipment IDs and monitor Calibration status.

Skills

Validation

Qualification

SOP Review

Documentation

Tools

URS

DQ

IQ

OQ

PQ

Job description

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

7 - 11 Years

PERMANENT

Job Description

• 1.Preparation and Review of Validation and Qualification related SOP’s.
• 2.Execution and verification of Qualification Activity at the departments levels
• 3.To ensure the preparation and Review of URS/DQ/IQ/OQ/PQ related to all new system and equipment to be installed at the site.
• 4.Preparation and review of Validation and Qualification related Protocols and Reports.
• 5.To investigate, evaluate and conclude the non-conformance / deviation related to validation and qualification.
• 6.To prepare Annual Validation Master Planner and to track and update the same, time to time.
• 7.Issuance and control of Validation and Qualification related documents.
• 8.Preparation, review and execution Cleaning Validation protocol and report.
• 9.Preparation, review and execution Process Validation protocol and report.
• 10.To review the protocols and reports for the Microbiological related testing and Analytical Method validation related activities of QC Laboratory.
• 11.To ensure the allotment of Equipment ID to all new equipment to be installed.
• 12.To ensure the Validation and Calibration Status of the equipment at the Site.
• 13.Preparation of Media Fill Protocols and Reports.
• 14.To participate in Media Fill activities and ensure the review and compliance of the activity as per the Batch Records and Protocols

Job Snapshot

Updated Date

21-09-2026

Job ID

JOB_1384

ONCOLOGY FORMULATION PLANT

Location

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