Technician
On-siteAll, Catalunya, Kingdom of Spain
All, Catalunya, Kingdom of SpainOn-siteFull TimeEnterprise
Full TimeEnterprise
Job Summary
Authorize signing for Parenteral GMP documents and equipment/area cleaning logs. Manage equipment qualification and re-qualification activities across the Vial Filling Line, PFS Filling Line, Infusion bag line, and API aseptic area. Oversee aseptic area and Freeze Drying area qualification and re-qualification processes within the Parenteral Manufacturing Area. Execute any additional tasks assigned by the superior. Requires 3+ years of experience and an ITI or Diploma qualification.
Required Qualifications
- 3+ years experience
- ITI / Diploma qualification
- Authorized to sign Parenteral GMP documents
- Authorized to sign Equipment and Area cleaning/sanitization logs
- Involved in equipment Qualification / Re-Qualification activity
- Responsible for Vial Filling Line
- Responsible for PFS Filling Line
- Responsible for Infusion bag line
- Responsible for API aseptic area in Parenteral Manufacturing Area
- Responsible for aseptic area and Freeze Drying area related qualification / requalification activities in Parenteral Manufacturing Area
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