Senior Associate QA (GMP)

The Company
Our client is one of the leads from the Biotechnology industry who try to improve patients’ lives, by distributing their medicines to hospital and pharmacies in 100 different countries in the world, to over 10 million patients, in Europe, Turkey, Middle East and Africa Regions.

Role Description
As an Associate QA you will be responsible for Perform complaint assessments in accordance with internal procedures, regulatory guidelines and business performance objectives.

Responsibilities
– Initiate and own Minor deviations related to Complaints Lab activities.

– Provide QA oversight for Regulatory labeling in the WH

– Prepare metrics and own and maintain departmental performance boards.

– Perform assessments in support of complaint investigations (reserve sample inspection, Return sample inspection and Safety Features verification).
– Prepare, review and approve procedures or work instructions in compliance with corporate, site and regulatory requirements.

Requirements
– Master’s degree in Life Sciences or related field or the equivalent combination of education and/or experience.

– Typically a half year of related experience.

– Experience in Quality Assurance in pharmaceutical industry

– Accurate mindset, flexible and pro-active attitude

Other information
Are you interested? Feel free to contact me!