Job Title:
Engineer II, Validation

Req #:
4795BR

Job Description:
Validation of manufacturing equipment, facilities, utilities and computerized systems associated with the manufacturing of pharmaceutical or medical devices to assure compliance with cGMP's, FDA's and B&L's guidelines. Job assignments are to be completed without a considerable amount of supervision or coaching. Assume the responsibility for the GMP and Environmental Health and Safety procedure awareness, and compliance within the respective area.

Qualifications


Education:
BS in one of the following fields: Mechanical, Electrical, Chemical or Packaging Engineering, Microbiology or Chemistry. Experience: No less than 2 years of pharmaceutical validation experience. No less than 5 years total pharmaceutical experience. Manufacturing experience highly desirable. Other: Validation experience in an FDA regulated environment desired. Strong project management, organizational, analytical, computer, writing and communications skills. Knowledge of aseptic processing highly desired. Excellent logical/mechanical aptitude. Knowledge of cGMP regulations and latest validation guidelines required. Able to handle multiple priorities in a fast paced environment. Able to work extended/odd hours around manufacturing schedule is required.

Work Location FL - Tampa Relocation Available Yes

Status Full-Time