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GCP Quality Manager
SIRE 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!
Our client is a professional Pharmaceutical organization, based in Basel-Stadt Switzerland.
Our client is a strong Pharmaceutical company in Switzerland
Provide expert opinion on Clinical Quality Assurance for Clinical teams in the development unit. Contribute to implement the quality strategy for clinical quality.
Contribute to the implementation of the quality strategy
Interact with Clinical Team members to ensure Quality is consistently
Support strategic Quality & Business initiatives, including the design and implementation of respective quality/compliance activities
Facilitate effective communications by supporting the Global program Quality Leader
Together with the QA Head help to ensure that applicable clinical development processes and quality standards
Monitor effectiveness of implementation of applicable clinical development processes through KQIs
Ensure continued submission & inspection readiness for the respective related submissions
Support the Quality input and oversight for the execution of clinical trials under their responsibility
Support through open and effective communication and business partnering
Proactively contribute towards lessons learned information flow
Degree in Life Sciences, Pharmacy or Medicines. Advanced degree a plus
Fluency in English (oral and written)
At least 4 - 6 years of involvement in regulated activities, clinical development and QA positions; broad understanding of global expectations of Health Authorities in the area of Clinical Development; profound understanding of the science of product development
3 or more years experience in managing projects
Strong skills in GCP, quality and/or clinical development.
Strong project management skills desirable
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.