Job Overview
This role is crucial in ensuring the quality of our products and processes. It involves GMP documentation preparation, review, approval, and management of D2 system used onsite, as well as participation in training initiatives.
Key Responsibilities:
* Preparation, review, and approval of GMP documentation
* Management of deviation investigation reports and change control systems
* Compilation of annual product quality reviews and CAPA management
* Assistance with regulatory and customer audits
* Generation and reporting of Quality metrics monthly
* Participation in GMP and Continuous Improvement projects
Requirements:
* Bachelor's degree in Science or equivalent industry experience
* Relevant experience in a pharmaceutical or life science organization
* Strong problem-solving and attention to detail
* Good understanding of EU GMP
* Proficiency in speaking, comprehending, reading, and writing English
* Ability to work independently and as part of a team
* Experience in TrackWise, MES, SAP, LIMS, and MS Office applications
About Us
We are a global healthcare company that empowers people worldwide to live healthier at every stage of life. We are committed to creating healthier communities through education, outreach, and better access to treatment. Our inclusive environment values diversity, equity, and inclusion, offering competitive salaries, benefits, and career progression opportunities.