Description
Join a Market Leader:
Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market.
Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites.
Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life.
You will be responsible to:
- Prepare, review or approve analytical test methods to be executed by Analytical areas;
- Prepare and review the protocols for work to be excuted in QC Labs;
- Prepare and review reports related with work carried out within the QC Laboratory;
- Define analytical strategies to allow the resolution of analytical problems detected;
- Verify and approve the analyses performed within the Quality Control Production Group whenever necessary;
- Support technically the analysts when conducting investigations or troubleshooting in the analytical lab;
- An English fluent speaker;Hovione is a proud Equal Opportunity Employer
Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.