Quality Assurance Officer
Location: SwitzerlandSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Basel-Stadt Switzerland.
- Quality inspections
- Report audits
- Internal and External facility evaluations
- System Audits
- Data reviews
- Support release activities
- Execution and reporting of Process, Facility and Supplier audits
- Preparation and authorization of Quality Assurance Statements
- Preparation and management of study audit files
- Monitoring of follow-up on findings
- Advise in quality issues
- Involvement in Quality projects
- Working under GMP standards
- At least 3 years' of relevant Quality Assurance or manufacturing experience in the pharmaceutical industry
- Experience in investigations, change control, validation and/or audits
- Good knowledge of Good Manufacturing Practices (GMP)
- Good understanding of English, German and preferable French
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Helene de Vries
The Company
This company is bringing word wide innovative science. Transforming individual lives and together with the team achieving the best possible results. As a part of this team you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career,Role Description
As a Quality Assurance Officer you assure compliance with regulatory requirements and internal procedures via appropriate oversight and planning, conducting and reporting:- Quality inspections
- Report audits
- Internal and External facility evaluations
- System Audits
- Data reviews
- Support release activities
Responsibilities
- Planning, execution and reporting of study audits for the customer- Execution and reporting of Process, Facility and Supplier audits
- Preparation and authorization of Quality Assurance Statements
- Preparation and management of study audit files
- Monitoring of follow-up on findings
- Advise in quality issues
- Involvement in Quality projects
- Working under GMP standards
Requirements
- Minimum Bachelor in a relevant field- At least 3 years' of relevant Quality Assurance or manufacturing experience in the pharmaceutical industry
- Experience in investigations, change control, validation and/or audits
- Good knowledge of Good Manufacturing Practices (GMP)
- Good understanding of English, German and preferable French
Other information
Want to know more? Contact me via the details below!Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Helene de Vries
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