Qualification Engineer Consultant
Location: SwitzerlandSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Basel-Stadt Switzerland.
Bio-pharmaceutical company with several cell lines that produces for external clients. It is a mid size with big expanding plans. It combines a family atmosphere with a strong interaction with international clients.
ROLE DESCRIPTION
The purpose of the Qualification Engineer Consultant is to develop a Qualification plan and ensure the quality of the equipment and infrastructure fulfils a the required standards.
- Starting date: ASAP
- Type of contract: temporary or temporary + possibility of permanent employment afterwards
This means that the company is open to hire a consultant for 6 months or a professional immediately available open for a temporary contract of 6 months that becomes a permanent employment afterwards.
RESPONSIBILITIES
- Preparation and execution of Qualification plans
- Ensure the quality of equipment and infrastructure
- Implementation of risk assessments
- Maintenance of technical documentation, equipment and devices
- Performance of calibration
- Develop SOPs and active contribution to Quality related tasks
REQUIREMENTS
- Technical or scientific background
- Previous experience in the biotech or pharma industry within GMP
- +5 years of previous experience in a similar role (recent)
- CSV experience is appreciated
- Fluent in English, fluency in German is a big plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
