Senior 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.
- Investigate complaints
- Drawing, analyze and track CAPA's, reporting to clients if required
- Performing internal audits
- Plan and execute quality control activities
- Suggest process improvements
- Facility while ensuring compliance with all existing GMP and safety standards in the area of responsibility
- Analyze change requests, review the class of change, determine the impact on the organization
- Drafting and updating of quality agreements with customers and suppliers
- A minimum of 3-5 years of experience in Quality in the pharmaceutical industry
- Knowledge of GMP
- Accuracy, tidiness, teamwork, eye for detail
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
The Company
Our customer is one of the largest supplier of medicines in the Netherlands. This is a unique opportunity to work in one of the largest pharmaceutical companies in the world!Role Description
The Quality Specialist will be focused on managing the Complaint Handling and Corrective Action Preventive Action (CAPA) processes. This position requires the ability to drive improvement across multiple functional areas and locations. The Quality Specialist must be a good problem solver and relentless in ensuring the root cause of the problem is addressed. Good judgment skills are necessary to ensure the appropriate balance of quality, compliance, and business needs.Responsibilities
- Release/Rejection of the batches- Investigate complaints
- Drawing, analyze and track CAPA's, reporting to clients if required
- Performing internal audits
- Plan and execute quality control activities
- Suggest process improvements
- Facility while ensuring compliance with all existing GMP and safety standards in the area of responsibility
- Analyze change requests, review the class of change, determine the impact on the organization
- Drafting and updating of quality agreements with customers and suppliers
Requirements
- Master's degree or equivalent experience- A minimum of 3-5 years of experience in Quality in the pharmaceutical industry
- Knowledge of GMP
- Accuracy, tidiness, teamwork, eye for detail
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
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