Interim Quality Specialist
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 Biotechnology organization, based in Nordrhein-Westfalen Germany.
My client, a innovative and internationally acting pharmaceutical company, is currently looking for Interim Quality Specialist due a maternity leave. The position is located in Cologne and is to be filled immediately for the duration of 12 months.
ROLE DESCRIPTION
You will work together with the Head of Quality and the global QM department to implement the QMS strategies and harmonize and standardize the QMS across all sites.
RESPONSIBILITIES
Assist the Global QMS team in the development and maintenance of the global QMS
Work with the sites to develop and implement local Quality Management Systems in compliance with the global QMS
Collaborate closely with site and global documentation managers for Change control and CAPA activities
Workshops and employee training in quality matters
Contribute to frequent discussions aimed at the continuous improvement of the QMS
REQUIREMENTS
University degree in a technical field like Chemistry, Biochemistry or Engineering,
Several years of relevant work experience with ISO standards and ICH guidelines as well as other Quality Management Systems references
Multiple years' experience within the pharmaceuticals production environment and very good GMP knowledge
Ability to communicate in an international environment and motivating colleagues from other departments
Excellent spoken and written command of English and good language skills in German
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.
