Req ID
Quality Assurance Specialist
Quality Assurance Specialist
2108 Couvet
Canton Neuch√Ętel

Company Overview
Established in 1921 in Switzerland, Sintetica is a pharmaceutical company delivering injectable anesthetics and analgesics to patients worldwide, through innovative science and excellence in development, production and marketing. Our people are the biggest asset. That is why we believe in the great place to work culture that promotes creativity, informed risk-taking, an exciting environment and a good feeling in everyday work.

• Analysis and evaluation of monitoring data and key performances indexes in order to insure a continuous improvement of the quality system
• Complaints management
• Deviation management
• Quality investigations and definition of corrective and preventive actions
• Supplier qualification for finished and semi-finished products, materials, raw materials and their periodic requalification
• Issuance of Master Batch Records
• Issuance of validation and qualification protocols and reports
• Definition of standard operating procedures and GMP-related documentation along with other involved Units/Department Managers
• Definition of training plans for employees along with other involved units/departments Managers
• Execution of batch record review
• Involvement in self-inspections
• Involvement in third parties inspections
• Issuance of GMP related documents (risk analysis, technical reports, etc.)

Position Description
For our production site in Couvet (Val de Travers - Canton Neuchâtel) that focuses on bags and vials anesthesia products, we are looking for a full time Quality Assurance Specialist.
This position supports the QA Manager by establishing and maintaining the Corporate Quality System.

Qualification and Skills
• Bachelor/Master degree in related technical science (Chemistry, Pharmacy or equivalent)
• Knowledge of the pharmaceutical industry and expertize in pharmaceutical manufacturing and GMP procedures
• 5 or more years experience in the Pharmaceutical field, Production or Quality Assurance (experience gained preferably in small-medium Pharmaceuticals)
• Fluency in French and English (the knowledge of Italian would be an asset)
• Strong relational, communication and adaptability skills
• Strong organizational, analytical and problem solving skills
• Ability to work independently and as part of a team
• 360° commitment to develop expertise on activities requiring high flexibility

We offer 

Fulltime permanent employment and extensive development opportunities within a dynamic and strongly motivating business environment.

For additional information please contact:
Corporate Sustainability/HR Department
+41(0)91 640 42 50

To apply for this position:
Applications can be submitted electronically via this official online form
Removal Date
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