Job Title
Join a Market Leader at Hovione, an independent family-owned international group of companies.
We are 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. We have over 1950 team members, from 36 different nationalities, located across Asia, Europe and North America.
Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients.
About the Role
* Define and implement quality control techniques to verify the quality of raw materials, intermediate and end products.
* Manage and control all Quality Control activities in accordance with identified quality assurance standards.
* Rigorously manage, execute and support all assigned projects in accordance with applicable GMP, quality operational standards / procedures and legal regulations.
You will be responsible for ensuring that all assigned analytical tasks are well managed and delivered on time, safely, efficiently, reliably and in a cost-effective manner.
Requirements
* A Master's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar field.
* Typically requires 3-5 years of relevant experience in a pharmaceutical QC laboratory environment.
* Hands-on experience in Analytical Chemistry and QC procedures is mandatory.
You must have strong understanding and knowledge of GMP practices, analytical theory and techniques.
About Us
Hovione is a proud Equal Opportunity Employer.
Inclusion and diversity are key to us. At Hovione, we value a work environment where differences are valued, and everyone is treated with fairness and respect.