validation Engineer at Al Alamia Veterinary Medicines Manufacturer
Al-Ayn, , United Arab Emirates -
Full Time


Start Date

Immediate

Expiry Date

08 Dec, 25

Salary

0.0

Posted On

09 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Validation, Biotechnology, Cleaning Validation, Manufacturing, Chemical Engineering, Analytical Method Validation, English, Computer System Validation, Pharmaceutical Engineering, Arabic, Equipment Qualification

Industry

Pharmaceuticals

Description

REQUIRED SKILLS & EXPERIENCE

Strong hands-on experience in validation with:

  • Equipment qualification (IQ/OQ/PQ).
  • Process and cleaning validation.
  • Analytical method validation and GMP documentation.
  • Troubleshooting and improving validation systems in industrial environments.
  • Prefer: Computer System Validation (CSV) and ERP/lab system compliance.

PREFERRED QUALIFICATIONS

  • Bachelor’s degree in Pharmaceutical Engineering, Chemical Engineering, Biotechnology, or related field.
  • 3–5 years of validation experience in pharma, veterinary, biotech, or feed manufacturing.
  • Familiarity with EU/FDA/WHO GMP validation guidelines.
  • Experience handling validation projects for new equipment or facility expansions.
  • Strong knowledge of industrial quality systems and audit compliance.

ADDITIONAL REQUIREMENTS

  • Must be able to relocate or commute to Al Ain before starting work.
  • Language: English (Required), Arabic is a plus.
    Job Type: Full-time
    Pay: AED4,000.00 - AED7,000.00 per mont
Responsibilities

ABOUT THE ROLE

We are seeking a skilled and detail-oriented Validation Engineer to join our growing team in Al Ain. This is an on-site role in a dynamic veterinary pharmaceutical and feed-additive manufacturing facility, ideal for someone with hands-on experience in validation of equipment, processes, utilities, cleaning, and computerized systems.

KEY RESPONSIBILITIES

  • Lead and execute validation and qualification activities across equipment, utilities, processes, cleaning, and computerized systems.
  • Develop and maintain the Validation Master Plan (VMP).
  • Prepare and perform IQ, OQ, and PQ protocols in compliance with GMP standards.
  • Document all validation activities, generate audit-ready reports, and maintain regulatory compliance.
  • Conduct risk assessments and recommend improvements to ensure system reliability and compliance.
  • Support cross-functional teams (QA, QC, R&D, Engineering, and Manufacturing) in validation-related activities.
  • Investigate deviations and implement CAPA (Corrective and Preventive Actions).
  • Provide training and technical guidance to staff on validation procedures.
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