Quality Assurance Technician
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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