Freelance QA/RA Manager
Location: GermanySIRE 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 Baden-Württemberg Germany.
My client, an innovative and internationally acting service provider for the pharmaceutical industry, is currently looking for a Quality and Regulatory Affairs Manager on a freelance base. The position is located in the greater Ulm area and is to be filled immediately for the duration of eight months.
ROLE DESCRIPTION
As Freelance QA/RA Manager you will lead interim wise the QM and RA team. Furthermore you'll be the responsible for the submission of the pharmaceutical products. You will ensure all quality processes and systems are implemented and maintained in accordance to industry standards and regulations.
RESPONSIBILITIES
Ensure the maintenance and development of the current QMS
responsibility for conducting SOP's as well as CAPA- and Change-Management
Be an expert in international regulatory aspects of importing and exporting pharmaceutical products and act as an contact point for regulatory matters
Develop and maintain knowledge of industry trends and developments through practical experience and knowledge gathering, interpreting the regulations on a product and country level
Deliver multidisciplinary regulatory and product delivery feasibility reports
REQUIREMENTS
University degree in Pharmacy or a related science
Several years relevant working experience within the pharmaceutical industry
Very good knowledge of quality and regulatory aspects within an GMP regulated environment is mandatory
Very good German and English language skills.
Project Management experience and able to travel internationally (up to 50%)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Matthias Kunkel.
