(Sr.) Specialist, LS & ASAT, Biologics
Roche View all jobs
- Shanghai
- Permanent
- Full-time
- The role supports on the equipment/system qualification and validation, sample/material management and QC operation readiness and start up.
- Work independently and with a level of autonomy and authority in efficient execution to ensure on-going compliance against approved global/local procedure documents, current Good Manufacturing Practices, and CN/EU Annex-1 during the product lifecycle.
- Enable and self-motivate, and demonstrate leadership behavior and mindset
- Perform the qualification, validation, calibration and maintenance activities for relevant equipment with Roche’s QMS and regulatory guidelines.
- Set up master data according to business requirements and ensure data integrity.
- Adhere to all effective SOPs and safety requirements and document laboratory work consistent with cGMP requirements
- Assist Head of Lab Support to complete GMP Self-Inspection as well as the relevant CAPAs to maintain the global level of GMP compliance.
- Presents technical analytical data clearly and concisely to internal investigations and regulatory inspectors. Accomplish sample and testing materials management(eg account management, DI assessment), to ensure they are in good order to meet the analytical needs any time. Report the abnormal status, deviations to supervisors with initiative.
- By identifying abnormal status and unexpected results during routine operation by detailed data, support to alert supervisors to investigate and solve the problem in correct way and in time.
- Maintain laboratory cleanliness and inventory of bioanalytical materials and cell supplies Supports lean initiatives in the area of lab operations, test method execution, documentation updates and equipment qualification
- Equipment qualification and validation: Support and execute the equipment qualification and validation for the aseptic product.
- Sample and material management: Execute GMP sample management; Execute material inventory management.
- Digital system deployment: Support and ensure on time delivery for QC digital system(eg.LIMS).
- Bachelor’s Degree (Life Sciences, Microbiology, or Analytical Sciences is preferred) and above
- 2 or more years of QC experience, QC experience, with a focus on bioanalytical and bioassay testing. MNC Bio-pharma experience is preferred
- Sound knowledge of quality control procedures and legal standards, with experience in aseptic assurance and physical and chemical testing.
- Experienced in QC new system startup readiness and operation ramp up is preferred.
- Fluent communications skills in English
- Project management skills are preferred.