Description
Responsibilities- Generate validation IOQ prototol/test plan for control systems
- Perform testing for cell culture and purification system
- Generate and facilitate the resolutions to any deviations during the execution
- Generate and facilitate the review and approval of the validation summary reports
- Minimum 3 years in GMP manufacturing validation engineering
- Computer skill such as Microsoft Excel, Outlook
- Strong writing and speaking communication skills in English
- Experience with manufacturing control systems such as SCADA systems (Intermediate)
- Experience in cleaning validation and steaming validation
- Experience in taking swab samples and rinse samples
- The following experience is preferred to have: experience in Validator 2000
- Experience with validation on the site
- Biopharmaceutical
- Manufacutring
- MS Office
- IQ/OQ Engineering Specification Documents
Synectics is an Equal Opportunity Employer.