Interim QA 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 Hessen Germany.
My client, an innovative and internationally acting pharmaceutical company, is currently looking for a QA Manager on an interim base. The position is located in the Frankfurt area and is to be filled immediately for an duration of 6 months.
ROLE DESCRIPTION
In the role as Interim QA Manager you'll be responsible for the implementation and maintenance of the QMS. Furthermore you'll maintain and improve the global SOP system.
RESPONSIBILITIES
Develop and implement a global audit plan
Support the development of a global QA strategy
Conduct and report gap analysis audits
Oversee execution of global audit plan and CAPA management as well as follow ups
Perform risk assessment and evaluation of global vendors/third parties
Implement all necessary tools to evaluate the process quality
Update and maintain relevant sections of the System Master File
Review and approve SOPs as well as manage the evaluation of existing SOPs
REQUIREMENTS
University degree in Pharmacy, Chemistry or a related field
Multiple years relevant experience in international pharmaceutical and/or biotech industry
Expert knowledge of current GMP requirements as well as in depth knowledge of drug development processes
Multiple years auditing and QA experience
Knowledge of document management/quality systems
Very good language skills in German and English (orally and written)
Ability 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.
