Quality Assurance GMP Associate

Company Description

Bioplan is a leading company providing GMP and GDP Quality Assurance System services to local Israeli pharmaceutical sectors, including supporting QP and PV functions for Manufacturers, Importers and GMP warehouses

With a focus on quality and excellence, Bioplan is committed to adhering to Good Manufacturing Practices (GMP) that ensure top-notch products are delivered to local customers, via QA services that meet EU mutually recognised industry standards. Located in Caesarea, we prefer to offer our full-time, onsite positions to those residing within the geographical radius of Haifa in the North, to Natanya in the South.

Role Description

This is a full-time, on-site role for a Quality Assurance GMP Associate located in Caesarea. The chosen candidate will oversee quality assurance processes, ensure compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP), and work closely with various Bioplan RA departments in order to maintain high quality standards. Daily tasks include monitoring and actively reviewing GMP/GDP ongoing processes, managing Good Documentation Practices, implementing core quality assurance process initiatives, monitoring validation documents, whilst maintaining proper documentation and ongoing reporting.

This onsite role is only suitable for professionals with a proven Pharmaceutical QA background and is not suitable for hybrid work

Qualifications

• Proficiency in Pharmaceutical Core Quality Assurance methods
• Excellent Communication skills, both written and verbal, for effective collaboration across teams
• Knowledge of Pharmaceutical GMP/GDP regulations and standards is essential
• NLT Bachelor's degree in Life Sciences, Biotechnology, Chemistry or a related field
• Detail-oriented mindset with the ability to identify and resolve quality-related issues
• Experience in the pharmaceutical or biotechnology industry is an advantage
• Excellent English language capabilities