Job Details
Do you have some years of experience in Quality Assurance in pharmaceutical environments? Do you have knowledge in validation/qualification, deviation, and CAPA management? Then you should read the following lines!
One of our clients, an international pharmaceutical company, is looking for a:
Quality Assurance Officer
Contact type: permanent
Location: Neuchatel Canton
Your Tasks:
- Monitoring data and key performances indicators in order to insure continuous improvement of the quality system
- Complaints and Deviation management
- Quality investigations and definition of CAPAs
- Supplier qualification for finished and semi-finished products, materials, raw materials and their periodic requalification
- Issuance of Master Batch Records, and validation and qualification protocols and reports
- Definition of standard operating procedures and GMP-related documentation along with other involved units/ department Managers
- Execution of batch record review, validation, and qualification of equipment utilities and machines
- Involvement in self- and third parties’ inspections
- Issuance of GMP related documents (risk analysis, technical reports, etc.)
- Change Control
Your Profile:
- Bachelor/Master degree in related technical science (Chemistry, Pharmacy, Engineering, or equivalent)
- Already experience in the Pharmaceutical field, Production or Quality Assurance. Experience gained preferably in small-medium Pharmaceuticals with marketing authorization (GMP certificated) released by the local health authorities.
- Knowledge of the pharmaceutical industry
- Expertise in injectables production both aseptic and terminally sterilized processes advantageous
- French and English Fluent
Do you have some years of experience in Quality Assurance in pharmaceutical environments? Do you have knowledge in validation/qualification, deviation, and CAPA management? Then you should read the following lines!
One of our clients, an international pharmaceutical company, is looking for a:
Quality Assurance Officer
Contact type: permanent
Location: Neuchatel Canton
Your Tasks:
- Monitoring data and key performances indicators in order to insure continuous improvement of the quality system
- Complaints and Deviation management
- Quality investigations and definition of CAPAs
- Supplier qualification for finished and semi-finished products, materials, raw materials and their periodic requalification
- Issuance of Master Batch Records, and validation and qualification protocols and reports
- Definition of standard operating procedures and GMP-related documentation along with other involved units/ department Managers
- Execution of batch record review, validation, and qualification of equipment utilities and machines
- Involvement in self- and third parties’ inspections
- Issuance of GMP related documents (risk analysis, technical reports, etc.)
- Change Control
Your Profile:
- Bachelor/Master degree in related technical science (Chemistry, Pharmacy, Engineering, or equivalent)
- Already experience in the Pharmaceutical field, Production or Quality Assurance. Experience gained preferably in small-medium Pharmaceuticals with marketing authorization (GMP certificated) released by the local health authorities.
- Knowledge of the pharmaceutical industry
- Expertise in injectables production both aseptic and terminally sterilized processes advantageous
- French and English Fluent