Find a jobRecruiters

Qa Executive

Exclusive opportunity

Onsite

Qa Executive

Utkarsh Placement

Qa Executive

Skills

Testing & QAGitCompliance

1 month ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

Important information


Contract type:

Permanent

Location:

Dera Bassi, Punjab, India

Work mode:

Onsite

Published on:

19 September 2026

What they need


Job Description QA Executive /QA Officer/ Sr. QA Officer

Location: Dera Bassi, Punjab
Department: Quality Assurance
Industry: Pharmaceutical API Manufacturing
Experience: 3–5 years in API Quality Assurance
Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.

Key Responsibilities

  • Prepare, review, revise and control QA documents as per cGMP and regulatory requirements.
  • Review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), logbooks and analytical documentation.
  • Handle deviations, incidents, CAPA, change controls and root-cause investigations.
  • Prepare and revise SOPs, formats, protocols and other quality-system documents.
  • Manage document issuance, retrieval, archival, version control and record retention.
  • Conduct shop-floor monitoring, line clearance and in-process compliance checks.
  • Support equipment qualification, process validation and cleaning-validation activities.
  • Review calibration, preventive-maintenance and qualification records.
  • Ensure compliance with data-integrity requirements and ALCOA+ principles.
  • Participate in internal, customer and regulatory audits and support closure of audit observations.
  • Coordinate with Production, QC, Warehouse and Engineering departments on quality-related matters.
  • Conduct or coordinate cGMP and SOP training and maintain training records.
  • Ensure timely completion and closure of all assigned quality-system activities.

Candidate Profile

  • Must have 3–5 years of QA experience in an API manufacturing facility.
  • Strong knowledge of cGMP documentation and pharmaceutical quality systems.
  • Hands-on experience with deviations, CAPA, change controls, investigations and batch-record review.
  • Familiarity with regulatory standards such as WHO-GMP, ICH, USFDA or EU-GMP.
  • Good documentation, communication and cross-functional coordination skills.

Please share me your updated resume at: [email protected]

Other offers great for you!

These companies are also looking for great profiles

Tenth Revolution Group

QA Engineer

Freelance

Ghent, Belgium

Hybrid

Skills

QA Engineer

3 months ago

Quick apply

5 Degrés

QA Engineer technico-fonctionnel

Permanent contract

Neuilly-sur-Seine, France

Hybrid

Skills

Testing & QAQA Engineer

2 months ago

Quick apply

Tenth Revolution Group

QA Engineer Automatisation (Playwright / Cucumber)

Freelance

Paris, France

Hybrid

Skills

GraphQLPlaywrightGitHubNotionQaseLinearClaude / Claude Code

4 days ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools