- Clinical Supplies Programme Manager
A fantastic and immediate need has arisen at a global pharmaceutical company for a Clinical Supplies Programme Manager on a contract basis to represent the Global Trial Supply Chain.
- Global Project Manager - Device Development (m/f)
Global Project Manager - Device Development (m/f)office-based in BaselRole:* As Global Project Manager for device development you are responsible for the coordination of global development projects with both internal as well as external stakeholders* In those development projects you define and implement the strategy for technical development * Moreover you monitor the implementation of manufacturing processes * You also coordinate usability engineering activities and support the scale up of ...
- Quality Assurance Manager (IMPs) - French Speaker
Our client, a company dedicated to development and production of biopharmaceutical products based in Belgium is looking for a "Quality Manager (IMPs)" to join their Brussels site. ABOUT THE DEPARTMENT ?The position is available within the department in charge of the manufacturing (primary, formulation, filling and packaging operations) and supply of all clinical lots for phase II and III studies and of stability batches to support registration of new products. ...
- Technical Manager
I am looking for a dynamic Technical Manager to join a successful Pharmaceutical organisation based in London, who are renowned for their high Quality standards. This would be a great opportunity to develop both your Quality and Regulatory experience, a rare and excellent opportunity to cross-skill. ...
- Clinical Supplies Manager – UK South East
This is a new opportunity to join a growing specialist Medical Device company as part of their trial supplies team. This role will be responsible for driving and managing all aspects of the clinical product supply chain for international studies both internally and with vendor oversight.
- Quality Compliance Manager - Cork - Permanent
QA Compliance Manager/ Qualified Person - Cork - Permanent
Optimus Search is currently in partnership with an internationally recognised Pharmaceutical company looking to recruit an experienced QA Compliance Manager and Qualified Person at their site in Cork.
- Senior Global Quality Assurance Auditor - Contract – UK
This company is looking to hire a self-motivated and dynamic individual with experience in Quality Assurance. The ideal candidate will be driven to work in a challenging environment with a leading pharmaceutical company and be motivated to stretch their technical skillset with others in a highly stimulating quality assurance role. This role offers an extremely competitive pay package and a fantastic opportunity to work with world leaders within the field.
- QA/GMP AUDITOR 5+ YEARS EXPERIENCE – NEW YORK
My client are a large-scale developer and manufacturer of generic and special drugs headquartered in New York, USA. Currently, my client are looking for an experienced QA/GMP Auditor to join their team in New York on a permanent basis.
- Quality Assurance Technical Coordinator
An attractive job opportunity has arisen at a leading multinational pharmaceutical company who are seeking a Quality Assurance Technical Coordinator to work at their UK site in the South-West. The company employs 100,000 personnel across 150 countries, working across multiple therapy areas including cardiovascular, oncology, and respiratory. This is a 6 month contract role with the possibility of an extension. ...
- Global Quality Auditor
This position entails performing routine GMP Audits as well as specialty and technical audits in relation to current products and prospective in-license agreements, providing compliance guidance and support throughout the Quality and Compliance organization, training delivery, and leading multi-departmental teams and initiatives. ...