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Validation Engineer

Job in Vereeniging, 1904, South Africa
Listing for: Placements24
Full Time position
Listed on 2026-10-17
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
  • Pharmaceutical
    Quality Engineering, Pharma Engineer, Regulatory Compliance Specialist, Pharmaceutical Manufacturing
Job Description & How to Apply Below
Location: Vereeniging

About the Role

Our client is looking for a detail-oriented Validation Engineer to join their facility in Vereeniging . This role is crucial for ensuring that all pharmaceutical manufacturing equipment, processes, and systems meet stringent regulatory requirements and are fit for their intended purpose. You will be responsible for planning, executing, and documenting validation activities, including IQ, OQ, PQ, and CSV. The successful candidate will have a strong understanding of GMP, validation principles, and a meticulous approach to documentation.

Your work will directly contribute to the safety, efficacy, and compliance of the pharmaceutical products manufactured by our client.

Key Responsibilities
  • Develop and execute validation master plans (VMP) and associated protocols (IQ, OQ, PQ, CSV) for pharmaceutical equipment, utilities, and processes.
  • Perform validation activities in compliance with GMP guidelines and regulatory expectations.
  • Write comprehensive validation reports, summarizing results and providing conclusions.
  • Collaborate with Engineering, Manufacturing, and Quality Assurance departments to ensure seamless validation processes.
  • Maintain validation documentation and ensure its readiness for regulatory inspections.
  • Investigate and troubleshoot any deviations or issues encountered during validation activities.
Requirements
  • Bachelor's degree in Engineering (Mechanical, Electrical, Chemical) or a related scientific field.
  • Minimum of 3-5 years of experience in validation within the pharmaceutical or related regulated industry.
  • Thorough understanding of validation principles, cGMP , and regulatory requirements (e.g., FDA, EMA, SAHPRA).
  • Experience with Computer System Validation (CSV) is highly desirable.
  • Strong documentation skills and attention to detail.
  • Ability to work independently and as part of a team.
Benefits
  • Competitive annual salary and potential for overtime pay.
  • Comprehensive medical and retirement benefits.
  • Opportunities for professional development and specialized validation training.
  • Work within a reputable pharmaceutical company known for its commitment to quality.
  • Generous annual leave and employee wellness programs.
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