Validation Engineer (qc, Pharmaceutical)

Singapore, Singapore

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Responsibilities:

Conduct cleaning validation activities with a specific emphasis on CIP for pharmaceutical manufacturing equipment and processes.
Develop and execute cleaning validation protocols, ensuring compliance with regulatory requirements and industry standards, especially in the context of procedures.
Collaborate with cross-functional teams to establish and enhance protocols, ensuring optimal cleaning efficiency and validation outcomes.
Perform risk assessments and gap analyses related to CIP processes and equipment.
Provide technical support to manufacturing teams, addressing CIP-related challenges and optimizing cleaning procedures.

Requirement:

Bachelor\'s degree in Chemical Engineering, Pharmaceutical Sciences, or a related field.
Proven experience in cleaning validation, specifically with a focus on CIP, within the pharmaceutical industry.
Strong understanding of regulatory requirements, including FDA and EMA guidelines, related to CIP processes.

Interested candidates can forward their CVs in MS Word format to alex@triton-ai.com

Reg No. R1549345

Triton AI Pte Ltd

License no. 21C0661

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