Validation Specialist/Writer

If you’re looking to begin a future in the world of science, Adecco is the best place to start. We have long-term temporary assignments that will put your college degree to work.

Adecco is the world’s largest staffing corporation. We have partnered with a renowned diagnostics corporation in Branchburg, NJ. We have long term, temporary Validation Specialist positions available.

The ideal candidates will be responsible for validation activities in a cGMP /CBER regulated medical device manufacturing environment. This position will perform validation activities for new and existing products, including the manufacturing and filling processes for bulk reagents, detection reagents, and PCR controls.

Duties will include writing of validation plans, protocols and reports. No lab work required.

Bachelor’s degree or Master’s degree, in a scientific discipline or related field; Experience preferred but not required. Academic excellence/high GPA is preferred. Independent projects/thesis work preferred. Excellent written and verbal communication skills with ability to multi-task are required, proficiency in MS Office applications preferred. References required.

For consideration please email your resume. Only qualified candidates will be contacted.

Adecco is an Equal Opportunity Employer (EOE).