Quality Assurance Specialist I to III

Quality Assurance Specialist I to III
Responsibilities & Duties:Responsible for giving disposition and reviewing executed batch and test records for clinical trials.
Maintains an Exception Handling report system and reviews received document reports that includes deviations, investigations, OOS, etc. Ensures completion of assigned action items with timely close-out.
Gives disposition to raw materials.
Works closely with other departments and performs area clearances.
Uses innovation and creativity to improve and develop new Quality Systems, departmental guidelines, and group activities/tasks.Minimum Requirements:Bachelor’s Degree in science or equivalent with Pharmaceutical, Biotech or related industry experience. (Note years of experience required per level: Level I: 1-2, Level II: 2-5 and Level III: 5-8.) Expertise in GMPs, ability to work with minimal supervision, excellent organizational and communication skills with ability to coordinate multiple tasks in a team environment, experience in Microsoft Office.ADA Notations:Ability to sit for long periods of time, handling, feeling with hands, reaching with arms.
Regular communication (hearing/speaking).
Lifting up to 25 lbs.
Occasionally works near moving or mechanical parts.
Routine office duties including computer keyboard use
Vision requirements include: close vision and ability to focus.
Noise conditions range from quiet to moderate. Contact Thelma Gerome email [Click here for email]
REQUIREMENTS
Please see job description.