Description
Cleaning Validation Specialist - Contract/FreelanceA Global pharmaceutical/biopharmaceutical organisation requires a competent, experienced Cleaning Validation Specialist to join their manufacturing facility based on West Coast of the USA.
The Role:
*Working to the Cleaning and Quality standards - Quality Modules, Quality Standards, VMP and SOP`s develop and execute, including sampling - in a timely manner - the relevant cleaning Qualification and Validation Protocols and Reports. This includes requalification activities.
*Ownership of cleaning validation related CAPAs previously identified during deviation investigations, audits, or inspections
*Timely and compliant execution of qualification activities
*Timely and compliant completion of qualification protocols and reports
*Participation in teams and projects which require cleaning or other validation expertise and input as dictated by the Validation Manager
Experience:
*Education - Bachelor`s in Engineering, Biology or related field or equivalent combination of education
*Min 6 years in a GMP environment, preferably with some medical devices - non sterile exposure.
*Demonstrated excellent oral and written communication skills; and must be able to work in both a team environment as well as independently.
*The position requires full-time, on-site support
*You must be a US Citizen or have the right to work in United States of America to be considered for this position.
An excellent daily rate is on offer alongside an exceptional opportunity to work for a Global pharmaceutical organisation based in USA.
Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this contract / freelance opportunity.