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 [email protected]
Reg No. R1549345
Triton AI Pte Ltd
License no. 21C0661
