Quality Manager/ Deputy FvP
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 Pharmaceutical organization, based in Luzern Switzerland.
Well-known pharmaceutical company with an affiliate in Luzern.
ROLE DESCRIPTION
Main representative to deal with the Swiss Health Authorities.
RESPONSIBILITIES
- Release commercial products independent from commercial functions
- Processing complaints defects in quality
- Processing quality defects, deciding on or possibly initiating measures necessary
- Taking decisions concerning destruction of returns Forwarding requests for exceptional re-use of returns
- Planning and monitoring of general GDP training of employees (initial training, GxP-awareness training).
- Quality oversight / auditing for external service providers (e.g. external warehouse).
- Contact person for Quality/Technical Agreements defining GXP responsibilities Decision making for all Quality issues.
- Maintenance of metrics and support the quality
- Regional Inspectorate, and the Cantonal Health Authority Meeting regularly with Swiss Logistic and Regulatory to assure alignment of activities
- Close cooperation with Pharmacovigilance Country
- Lead Participating in regular meetings with EMEA Regional Quality Operations
REQUIREMENTS
Scientific degree (pharmacy, medicine, biology or a comparable discipline)
Qualified or Responsible Person, preferably in Switzerland.
Eligible to be a Deputy Qualified Responsible Person in Switzerland
3 to 5 years of experience in Quality Assurance (GMP/GDP)
Fluency in German and English, (French is appreciated)
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.
