
Validation Specialist Position
7 days ago
Job Overview:
We are seeking an experienced Validation Specialist to join our team. In this role, you will be responsible for preparing and executing validation protocols for equipment such as CIP tanks, robotic cleaners, and utility systems.
Main Responsibilities:
- Develop and execute validation protocols (URS, IOQ, PQ, FMEA, PVP)
- Conduct cleaning validation, temperature mapping, and requalification activities
- Ensure timely delivery of validation documentation and compliance with project timelines
- Develop and review qualification documentation (DQ, IQ, OQ, PQ, SAT, QSR) in both paper-based and digital platforms
- Support validation of chemical production systems and cleanroom equipment
- Coordinate equipment change releases and ensure timely CR closures
Requirements:
- Degree related to Science or Engineering
- Good knowledge and experience in GMP facilities
- At least 5 years of experience in manufacturing, and biopharmaceutical industries
- Ability to multitask and work in a fast-paced environment with competing priorities
- Strong interpersonal and communication skills and ability to develop close working relationships and work collaboratively with internal and external contacts at all levels
- Exhibit continuous improvement mindset and innovative thinking
Benefits:
- Greatest exposure to the pharmaceutical industry
- Annual leave benefits
- Full Health coverage and benefits
- Training and Development allowance
About Us:
- A dynamic and collaborative work environment
- Ongoing training and development opportunities
- A competitive salary and benefits package
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