Deviation & investigation Consultants job in Chicago, Illinois

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This vacancy has now expired. Please see similar roles below...

Proclinical is working with a leading, Global Pharmaceutical company based in the US who are looking to add consultants to an existing quality department.

There are 4 open positions in Kansas and 3 in Missouri.

Extremely competitive salary/package

Job Responsibilities:

There are 2 FDA remediation projects. Same responsibilities at each site focusing on the contamination during the manufacturing process of injectable sterile drugs.

We have a batch block of 300+ Deviations open and in this role and you will work as a Consultant and act as a GMP Investigator.

All your activities will focus on root cause resolution;
You will be using the investigation tools for the identification of the correct root cause;
Training and support will be provided during the project.

Skills and Requirements:

Track wise
Deviation & investigation experience
GMP understanding
Work experience in sterile manufacturing processes
Good knowledge of the investigation tools

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 Ivan Gitardi on +44 203 0789 551 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.

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