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A leading biotech company based in Spain is seeking a dedicated QA Consultant to join their team as they transition into commercial readiness. This role offers the chance to make a significant impact by enhancing GMP efficiency and ensuring the highest standards of quality assurance.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Consultant will be varied; however, the key duties and responsibilities are as follows:
1. Manage and resolve deviations, ensuring all issues are addressed promptly and effectively.
2. Oversee CAPAs (Corrective and Preventive Actions) to prevent recurrence and maintain compliance.
3. Conduct workshops to train and develop staff, fostering a culture of continuous improvement.
4. Strengthen GMP (Good Manufacturing Practice) efficiency, ensuring all processes meet regulatory standards.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the QA Consultant, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in quality assurance within the biotech sector.
3. A working knowledge and practical experience with GMP regulations and quality management systems.
Key Words:
QA Consultant / biotech / Spain / commercial readiness / deviations / CAPAs / recurrence management / GMP efficiency / quality assurance / workshops
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
A leading biotech company based in Spain is seeking a dedicated QA Consultant to join their team as they transition into commercial readiness. This role offers the chance to make a significant impact by enhancing GMP efficiency and ensuring the highest standards of quality assurance.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Consultant will be varied; however, the key duties and responsibilities are as follows:
1. Manage and resolve deviations, ensuring all issues are addressed promptly and effectively.
2. Oversee CAPAs (Corrective and Preventive Actions) to prevent recurrence and maintain compliance.
3. Conduct workshops to train and develop staff, fostering a culture of continuous improvement.
4. Strengthen GMP (Good Manufacturing Practice) efficiency, ensuring all processes meet regulatory standards.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the QA Consultant, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in quality assurance within the biotech sector.
3. A working knowledge and practical experience with GMP regulations and quality management systems.
Key Words:
QA Consultant / biotech / Spain / commercial readiness / deviations / CAPAs / recurrence management / GMP efficiency / quality assurance / workshops
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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