Validation Consultant - Singapore - Triton AI Pte Ltd
Description
Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:- Process Equipment
- CIP / SIP
- Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations
- Method validation (analytical chemistry, biochemistry, microbiological)
- Enterprise system (LIMS, QMS)
- Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
- Develop validation protocols using a science and risk based approach that meets regulatory requirements and industry best practices.
- Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
- Investigate deviations, write investigation reports and create summary reports.
- Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
Requirements:
- Bachelor's degree in technical discipline such as Engineering or Science or with experience relevant to the Job Description. Graduates of related discipline may also apply.
- Minimum 3 years of experience in pharmaceutical industry
- Experiences in commissioning, qualification, validation, quality systems, quality operations, manufacturing, engineering, technology transfer.
- Foundational understanding of ICH Q7, Q8, ICH Q9, ISO 14644, ANSI Z1.4 and other regulatory requirements preferred
- Experience with investigations into manufacturing / laboratory deviations and determination of product impact potential, root cause and corrective/preventive actions.
- Strong knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
Benefits:
- Up to $6000 with 2 months Variable Bonus, Permanent Position
- West Singapore
- Pharmaceutical Industry Experience is a MUST
- Experiences in multiple CQV discipline (such as CIP, SIP)
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