Engineering Validation Specialist

Hobson Prior Ltd; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

Hobson Prior Ltd is seeking an Engineering Validation Specialist in London to ensure compliance with regulatory standards in biotechnology. The role involves reviewing validation documents and collaborating across departments, positioned within a growing company focused on healthcare advancements.

Qualifications

• Experience in a cGMP pharmaceutical/biotechnology setting.
• Knowledge of validation in engineering and computerized systems.
• Experience with utilities, equipment, and facilities.

Responsibilities

• Ensure all equipment and systems meet regulatory validation standards.
• Review approval processes for validation documents and protocols.
• Collaborate with departments to align validation with business goals.

Skills

cGMP environment

Computerized system validation

Validation compliance

Job description

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.

Hobson Prior is seeking an Engineering Validation Specialist to join a dynamic team in London.

In this role, you will ensure that all equipment, facilities, and computerized systems used in regulated processes meet the required standards. You will act as a subject matter expert on validation, ensuring compliance with EU, UK, and FDA regulations while supporting quality management activities.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Ensure all equipment, facilities, and systems are validated and compliant with regulatory requirements.
• Review and approve validation documents, protocols, and reports.
• Collaborate with various departments to align validation plans with business objectives.
• Support audits and inspections by acting as a subject matter expert.
• Address and resolve issues related to validation and compliance.
• Maintain inspection readiness and ensure documentation meets quality standards.
• Manage changes and deviations effectively, ensuring timely resolution.
• Stay updated on industry regulations and best practices.

Key Skills and Requirements:

• Experience working within a cGMP pharmaceutical/biotechnology manufacturing environment
• Knowledge of computerized system validation and engineering validation
• Experience working on utilities/equipment/facilities

For more information, please contact William Hay.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - (url removed)