Oferta


Quality Assurance Technician
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The candidate will be expected to be key member of the Quality Assurance.
The candidate will be expected to provide quality assurance oversight.
Proficiency and capability in managing activities in a fast paced environment is expected.
 
Assessment criteria:
• At least three years’ experience in Quality Assurance from a related industry, with a preference from within the biopharmaceutical industry.
• Draft quality assurance policies and procedures
• Experience training staff in Quality Assurance
• GMP experience
• Audit experience
• CAPA experience
• Ensuring Deviations, CAPA and Change Control are progressed in a compliant and timely manner
• Ensuring complaints and non-conformance issues are investigated in a compliant and timely manner
• Ensuring batches are reviewed and released as required to support business needs
• Participating and supporting internal audits
• Participating and leading risk assessments
• Knowledge of tools, concepts and methodologies of QA
• Capable to identify areas for improvement in the quality system and implement improvement actions
• Knowledge of relevant regulatory requirements
• Proficient verbal and written communicator.
• Proficiency to work within regulatory guidelines.
• Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment.
• Experience in the preparation and review of documentation (SOPs, Development Reports, Characterization Reports, Qualification reports, Validation Reports) in English to regulatory standards is essential.

Other requirements:
• Fluent in English.
• Willing to relocate to Northern Spain
Contact Email: rrhh@3pbio.com
WebSite: www.3pbio.com



 
 
 
 
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