Validation Executive

Closing on: Dec 24, 2026

Job role

Join a high-performing pharmaceutical team where you will lead commissioning, qualification, and validation activities for manufacturing equipment, utilities, and cleanroom systems. You will develop and execute validation protocols and reports, support system impact assessments, and ensure compliance with GMP and regulatory standards. The role also involves process, cleaning, and packaging validation, temperature mapping, and maintaining accurate documentation through QAMS/DMS systems, while contributing technical expertise to uphold product quality and operational excellence.

Qualifications

  1. Bachelor’s degree in pharmacy, chemical engineering, biotechnology, industrial engineering, or a related field; higher qualifications will be an advantage.
  2. 1-2 years of experience in the pharmaceutical industry.
  3. Strong knowledge of GMP and GDP standards. Additional certifications or training in Quality Management Systems (QMS) are a plus. Excellent communication and interpersonal skills, with proficiency in English (written and verbal).
  4. Ability to perform effectively in a fast-paced, results-driven environment.

When applying

Attractive remuneration package, transport and other benefits will be on offer. If you are confident that you possess the above requirements, we invite you to send your complete CV to reach us within 7 days of this advertisement.

Company: Navesta Pharmaceutical (Pvt) Ltd
Company email: [email protected]
Job Location: Nawala
Job Category: Pharmaceuticals / Biotechnology / Life Sciences
Job Type: Full Time

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