Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceuticals ingredients and finished dosage forms.
In Centrient Pharmaceuticals Ramos Arizpe we are looking for a Quality Leader for being part of a new project. This position will be responsible of manage the Quality System focused on the Quality Risk Management and Change Control System, ensuring regulatory and quality compliance of the improvements and changes to be implemented on the site.
To participate in the vacancy it is essential to fulfill the following requirements:
Requirements
* Bachelor degree in chemist pharmacobiologist, chemistry or pharmacist (indispensable both, document amp; chemical area)
* Advanced (fluent) english written amp; spoken
* 5- 7 years of minimum experience in:
• Quality Systems coordination, in management and analysis of Quality Risks and change controls in the pharmaceutical industry.• Regulatory activity, attention to regulatory inspections and monitoring of findings to obtain a GMP certificate.
• Handling deviations, CAPAS and complaints.• Validations, review and / or authorization of protocols and executive reports to management and CVS
• Statistical data analysis, trend analysis and process capabilities
• Leading Quality assurance topics in multidisciplinary projects