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Quality Assurance Senior Associate

West Greenwich, RI
Top 3 Must Have Skill Sets:    

Previous Quality experience in the Pharmaceutical and/or Medical Device industry.
Experience and training in electronic document management system, Trackwise, Maximo.
Demonstrated proficiency of written and verbal communication skills with ability to communicate and collaborate effectively with team and internal stakeholders.

Description:

Previous Quality experience in the Pharmaceutical and/or Medical Device industry.
Experience and training in electronic document management system, Trackwise, Maximo.
Demonstrated proficiency of written and verbal communication skills with ability to communicate and collaborate effectively with team and internal stakeholders.
This resource will be required to sit on-site at Rhode Island and will be responsible for Quality support of Manufacturing and related functional area activities. This position provides the opportunity to work directly with Operations staff during bulk drug substance operations. The shift structure is Monday-Friday (Admin shift) (8 hour/day).

"This posting is for Contingent Worker, not an FTE"

 

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