Responsibilities:
- Lead the commissioning and qualification processes for benchtop and process equipment
- Conduct qualification activities for analytical laboratory equipment, including HPLC and GC-MS.
- Author DeltaV recipes for system functionality.
- Develop MES (Manufacturing Execution System) recipes using platforms such as Siemens OpCenter / XFP, PAS-X, and Syncade.
- 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.
- Perform risk assessments and gap analyses related to CIP processes and equipment.
Requirement:
- Bachelor's degree in Chemical Engineering, Pharmaceutical Sciences, or a related field.
- Commissioning and qualification experience is a added advantages.
- DeltaV recipe authoring.
- MES recipe authoring (Siemens OpCenter / XFP, PAS-X, Syncade).
- Proven experience in cleaning validation within the pharmaceutical industry.
- Strong understanding of regulatory requirements, including FDA and EMA guidelines.
Interested candidates can forward their CVs in MS Word format to [email protected]
Reg No. R1549345
Triton AI Pte Ltd
License no. 21C0661
