Deviation Investigators, Sterile Manufacturing

Proclinical is in the process of building a project team to assist with deviation investigation within a pharmaceutical manufacturing facility in the Midwestern United States.

We are seeking qualified consultants to join the team who have a background in grade A sterile manufacturing. The successful applicants will have had experience of investigating and writing deviations relating to sterile process equipment such as lyophilizers, dry heat ovens, washers, aseptic fillers or autoclaves. The project can be offered on a W2 or 1099 basis.

The successful applicants will be degree educated and have experience of working in GMP regulated environment. They will have worked in grade A sterile conditions and have written and investigated deviations related to sterile/ aseptic processing equipment such as lyophilizers, dry heat ovens, washers, aseptic fillers or autoclaves. You should be a strong communicator who is able to influence change at all levels of of an organisation. Strong problems solving skills are essential.

The contract will be offered on a 6-month rolling basis

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 Owen Bach on +44 203 8261 330 or upload your CV 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.