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Job Title: Manufacturing Associate III (Fill Associate) (NCI)
Job Location: MD: Frederick
Pay Rate: Open
Job Length: full time
Start Date: 2008-03-24
Company Name: SAIC
Contact: HR
Phone: email only please
Fax: email only please
Description: Manufacturing Associate III (Fill Associate) (NCI) Full Time Regular posted 3/14/2008 Job Category BIO - Biopharm Mfg/Dev Req ID 111276 Able to obtain security clearance? None Currently possess security clearance? None Location Frederick, MD % Travel Relocation No Requirements Performs drug product component preparation, aseptic formulation and filling, inspection, and labeling activities under cGMPs for the Vaccine Pilot Plant. Responsible for planning production activities within assigned area. Assists in the development of budgets, schedules and performance requirements. Writes Standard Operating Procedures and reviews batch production records. Will serve as a lead technician within assigned area. Duties will include training others within the working group and providing feedback to the supervisor. Will interface with Quality Control/Quality Assurance and frequently interact with customers and/or Senior Management. REQUIRED SKILLS: Possession of Bachelors degree in a scientific/computer related discipline from an accredited college/university or four (4) years related experience in lieu of degree. Foreign educated candidates who have completed part or all of their education outside of the United States must have their foreign education evaluated by an SAIC-approved accrediting organization to assure that it has met the equivalency of the qualifications of degree work in the United States. In addition to educational requirements, a minimum of five years progressively responsible job related experience or a minimum of three years progressively responsible job related experience in a cGMP environment. Strong understanding of the regulatory issues associated with cGMP manufacturing of biopharmaceutical products; strong understanding of cGMPs as they related to manufacturing operations. Knowledge of cGMP operations, cleanroom environment and production isolators used for aseptic pharmaceutical filling. Ability to write and follow Standard Operating Procedures, assist in writing master batch records and complete Batch Production Records under Good Manufacturing Practices. Working knowledge of computer assisted manufacturing/production equipment. Ability to lift up to 35 pounds and work in a BL2 environment. This position is subject to obtaining a Public Trust Clearance. DESIRED SKILLS: Experience in isolation technology. Experience as lead technician in a GMP environment.
Please refer to Job code saic-111276 when responding to this ad.
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