We are a family-owned international group of companies, reaching over 1950 team members across Asia, Europe and North America. Our people are our main asset for continued success.
About Hovione
Our innovative technological and productive capabilities have positioned us as a top Contract Development and Manufacturing Company in the world market. We help Pharmaceutical Customers bring new and off-patent drugs to market.
Key Responsibilities
You will be responsible for:
* Defining and implementing quality control techniques to verify the quality of raw materials, intermediate and end products.
* Managing and controlling Quality Control activities according to quality assurance standards, company procedures and regulatory guidelines.
* Organizing daily priorities within assigned tasks to perform sample analysis accurately and promptly.
* Ensuring an efficient Quality Control system by adhering to the laboratory testing schedule.
* Taking responsibility for all data generated and ensuring it meets GMP requirements.
* Maintaining checklists, laboratory records and notebooks according to GMP standards.
* Maintaining good hygiene and housekeeping within the laboratory.
* Performing routine calibration and maintenance of laboratory instruments.
* Complying with high standards in the QC Laboratories.
* Reporting discrepancies, deviations or non-conformance in testing or work practice.
* Issuing events and supporting the investigation of OOS/OOT/atypical results, deviations and QC incidents.
* Communicating with internal departments regarding QC work.
* Assisting with audits as required.
* Undertaking additional tasks to support laboratory activities.
Requirements
To be successful, you must have:
* A qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field.
* Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment.
* Experience of GMP practices and HSE standards.
* A technical understanding of GMP practices, analytical theory and techniques.
* Clear and open communication skills.
* Competency in English (preferable).
* The ability and availability to work in shift patterns, as required by business needs.
* Computer literacy with knowledge of the MS Office package.