Quality Validation Specialist
(1 years contract)
About the Company:
Our client is a Swiss pharmaceutical based corporation that provides solutions to address the evolving needs of patients worldwide. Their main discoveries are development, manufacture and marketing of prescription and generic pharmaceutical products and eye care products.
Role Overview:
In this role, you will support the commissioning and qualification activities for the equipment/system/process until the system is released to the Manufacturing site use.
Key Responsibilities:
- Represents site QA Validation Subject Matter Expert (SME) for Computer System Validation (CSV)/Lab systems based on the assigned project
- Advice and guide stakeholders on non-routine and non-standard activities or plans to ensure projects are completed according to timelines and specifications
- Advise and resolve challenging issues relating to modifications of current processes and systems and qualification and validation approach within and across various functions to ensure all health, safety or training procedures meet requirements
- Review of deviations / non-conformances and lead the strategic discussion for investigations
- Oversight of assigned validation activities, ensures compliance with current Good Practice (cGxP), inclusive data integrity and eCompliance
Requirements:
- Diploma or Bachelor's degree in a scientific / technological background (e.g. Chemistry, Pharmacy, Biology, Biochemistry, or equivalent)
- At least 3 Years experience in Quality Validation/Operations within Pharmaceutical industry
- Good communication skills
- Ability to work well in a team environment.
Reg No: R22104540
EA License no: 94C3609
