Freelance QA Consultant
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 Hessen Germany.
My client, an international Pharmaceutical company, is currently looking for QA consultant on a freelance basis. The position is located in Marburg and ist to be filled immediately for a duration of eight months.
ROLE DESCRIPTION
In the role as Freelance QA/RA Consultant you are responsible for the documentation and compliance of Quality Management System as well as the implementation of QMS strategy and tactics. Furthermore you act as contact person for the notified body.
RESPONSIBILITIES
Oversee and assure the continuous compliance of the QMS
Responsible for SOP-Management
Represent the Quality department in global projects
Staff training in Quality matters as well as maintaining a training database
Act as a key contact for internal audits
Coordination of CAPA responses
Support regulatory agency inspections including pre-inspection and related follow-up activities
Contribute to audit and inspection readiness activities
REQUIREMENTS
University degree in the field of Pharmacy or a similar Life Science
At least 5 years of experience in managing QMS for the Pharmaceutical industry
Excellent knowledge of GMP regulations as well as experience in the submission of Pharmaceuticals
Very strong language skills in German and English (orally and written)
Ability to travel internationally
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.
