Description
A global biotech organisation is looking for x2 experienced Equipment Requalification Validation Engineers to work within the Vaccines and Diagnostics manufacturing facility, based in California.The validation engineers will interact with cross-functional teams including representatives from Manufacturing, Maintenance & Calibration, Technology Development and Quality to ensure scheduled requalification are complete as planned and production is not negatively impacted.
Responsibilities include:
-Working to the clients Validation and Quality standards - Quality Modules, Quality Standards, VMPs and SOP`s to develop and execute, in a timely manner, the relevant Requalification Protocols and Reports. This includes all requalification activities.
-Timely and compliant execution of Requalification activities
-Timely and compliant completion of Requalification protocols and reports
-Participation in teams and projects which require validation expertise and input as dictated by the Validation manager relevant to the appropriate Requalification activity
Experience Required:
-Bachelor`s in Engineering or related field or equivalent combination of education and experience,
-Experience in a GMP environment, preferably with medical device and biotech experience.
-Excellent oral and written communication skills, and must be able to work in both a team environment as well as independently.
This is an exciting opportunity for experienced Validation Engineers to come and join a fast paced environment. These positions are offering competitive rates of pay and are initially until the end of the year with possibilities of extensions. Please apply now for more information.