Job Duties:
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Planning and adjusting own schedule to meet priorities on a daily basis.
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Checking and reviewing data for accuracy and completeness independently.
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Interacting with group members to coordinate functions and maximize efficiency.
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Resolving routine manufacturing problems independently / utilizing the appropriate technical group resource and problem solving techniques.
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Communicating with vendors.
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Reading operation manuals and contributing to writing of SOP's.
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Contributing to preparation and completion of deviation reports.
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Communicating effectively in situations involving pressure.
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Demonstrating the ability to apply knowledge of the cGMP Regulations.
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Demonstrating knowledge and fundamental understanding of operating computer-controlled production equipment.
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Performing numerous tasks ranging from basic to complex functions.
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Demonstrating knowledge of applicable software.
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Performing inventory transactions and troubleshoots discrepancies.
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Recommending process/quality improvements.
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Offering innovative solutions to manufacturing problems.
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Recognizing and suggesting personal objectives which complement and support group and organizational goals. Influences others in meeting their group objectives through support and cooperation.
Education:
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Associates Degree in a science related field and 1-2 years’ experience in a pharmaceutical/biotech manufacturing environment or a High school diploma with 3 – 5 years work experience in a manufacturing and/or quality environment.