Hovione Overview
Hovione is an independent family-owned international group of companies that has set itself apart through innovative technological and productive capabilities. As a leading Contract Development and Manufacturing Company, we help Pharmaceutical Customers bring new and off-patent drugs to market.
Our success is built on the expertise of our team members from 36 different nationalities located across Asia, Europe, and North America. Working at Hovione means striving for innovation and excellence in everything we do: for our clients, partners, and patients.
Job Description:
The successful candidate will be responsible for defining and implementing quality control techniques to verify the quality of raw materials, intermediate, and end products, as well as providing analytical services relevant to our client base and according to regulatory requirements.
Main Responsibilities:
* Define and implement quality control techniques to ensure compliance with regulatory requirements.
* Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.
* FOLLOW THE DAILY PRIORITIES TO ACCURATELY AND PROMPTLY PERFORM THE ALLOCATED SAMPLE ANALYSIS.
* Achieve an efficient Quality Control (QC) system by adhering to the laboratory testing schedule.
* Ensure data generated complies with all applicable GMP requirements and HSE regulations.
* Maintain checklists, laboratory records, and notebooks to an acceptable GMP standard.
* Maintain good hygiene and housekeeping within the laboratory.
* Perform routine calibration and maintenance of designated laboratory instruments.
* Comply with high standards in the QC Laboratories.
* Brought any discrepancies or non-conformance to the attention of QC management.
* Issue events and support the investigation of OOS/OOT/atypical results, deviations, and QC incidents.
* Ensure appropriate communication with other internal departments.
* Undertake additional tasks to support laboratory activities as required.
Requirements:
* Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related, or science-related field (strong preference).
* Proven practical experience in a GMP regulated QC laboratory environment (preferable).
* Experience of GMP practices and HSE standards (preferable).
* Technical understanding of GMP practices, analytical theory, and techniques.
* Clear and open communication skills (written and verbal).
* Competent English language skills (preferable for sites where English is not the first language).
* Ability and availability to work in shift patterns, as required by business needs.
* Computer literacy with knowledge of the MS Office package.
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