Laboratory Equipment Qualification & Validation Lead - GMP

At Proclinical, we are seeking an individual to fill the role of Laboratory Equipment Qualification and Validation Lead, based in Boston, MA.

Responsibilities

• Generate and approve commissioning protocol.
• Execute commissioning protocol/discrepancy generation and resolution.
• Generate/approve commissioning final report.
• Generate and approve supplemental I/OQ protocol.
• Execute I/OQ protocols and conduct discrepancy generation and resolution.
• Generate/approve I/OQ final report.
• Manual soiling of glasswasher equipment with worst-case soil.

Skills And Qualifications

• BA in a related field and 2-4 years of relevant experience.
• Laboratory equipment qualification experience in a GMP environment.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Corrin Pyle at (+1) 2674358555 or upload your resume on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.