GBI-342: Manufacturing Associate II
The selected candidate will use good manufacturing procedures, GMP, to perform a variety of production line tasks to include part assembly, labeling, packaging, inspections and lot accountability. You will perform visual inspection on in process materials according to documented specifications, reject and segregate parts that do not meet specifications, assemble small parts and operate production line machinery and computers. You will perform elements of quality control during assembly and follow manufacturing operating procedures, MOP’s, MBR’s, WI’s etc. You will complete a daily production log, communicate effectively with co-workers and the department supervisor, clean and maintain the work area and turn off and lock out equipment when not in use. You will communicate with the supervisor of any excessive damaged or substandard assembly work and defective parts, tools, equipment, material or other conditions which hinder the assembly process. You will perform reconciliation and accountability of each production lot. You will assist in training new and existing personnel on all work stations/paperwork for the assembly processes and perform basic troubleshooting on equipment.

Qualifications include an AS degree or High School diploma and at least three years of related cGMP experience or equivalent combination of education and training. You must have the ability to effectively communicate in English both verbally and in writing and the ability to follow written and verbal instructions in English. You should be detail oriented with basic computer skills using MS Word, Excel and Outlook along with the ability to frequently lift up to 15 lbs and stand for long periods of time. You must be able to work a flexible schedule to include days, nights, weekends and overtime as needed. Manual dexterity is required for quick and accurate assembly of small parts and operation of equipment.
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GBI-334: Lead Manufacturing Technician
The selected candidate will direct daily activities in the manufacturing area and will manage priorities on shared resources to achieve the manufacturing needs. You will schedule production of work orders and work in progress to meet stated goals for capacity utilization, on time deliver and cost. You will coach team members on implementation of the manufacturing systems to drive cost and waste out of the systems. You will participate in a leadership role in plant wide activities such a s safety, employee satisfaction and continuous improvement. You will write and revise SOP's, MOP's, MBR's, work instructions and preventative maintenance documents. You will work to ensure preventative maintenance is kept on schedule and is documented for all manufacturing equipment. You will repair and maintain production and test equipment. You will operate manufacturing equipment during production runs as well as assist in validation of equipment and tools in manufacturing. You will be responsible for parts and materials purchasing selection, organize and maintain maintenance logs and train manufacturing personnel to operate equipment.

Qualifications include a minimum of a High School diploma or an AA degree with a minimum of two years experience in a cGMP environment in the biotech or pharmaceutical industries. Prior lead or supervisory experience is preferred. You should also be flexible to work with changing shifts for both day and swing shifts. Apply Now TOP MENU

GBI-331: QA Assistant
The selected candidate will assist the QA Lab Supervisor to perform functional testing of in process and final diagnostic products. You will perform general laboratory tasks, complete quality documentation for testing being performed, regularly clean the lab and work areas and coordinate with the Lab Supervisor in determining work assignments to meet production timelines. Other duties may be assigned as needed.

Qualifications include a BA/BS degree in the Life Sciences with the ability to carry out detailed written and oral instructions for testing of diagnostic products. You should be computer literate with very good written and verbal communication skills. You should also be detail oriented with excellent documentation skills. Apply Now TOP MENU