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Location: Oklahoma City, OK

Salary: $43,000 or based on experience

Days: Tuesday through Saturday (may vary based on laboratory needs)

Hours: 8:00 a.m. to 4:30 p.m. (may vary based on laboratory needs)

Position:

As a Supervisor of Manufacturing Operations in Blood Product manufacturing, you will be responsible for control of daily manufacturing operations for the Component Manufacturing, including all staff, environment and work processes. Ensure compliance with regulatory compliance with all regulations in accordance with AABB, CLIA, federal, state, OBI policies and procedures. Assure compliance with safety policies and procedures in the work area and use of applicable protective equipment at all times to prevent exposure to potentially infectious blood and body fluids. Manage blood component product manufacturing based on inventory and customer needs.

Qualifications:

• Position requires a Bachelors of Science from an accredited institution in chemical, physical, biological or clinical laboratory science; Education may be substituted by years of relative work experience
• 2-5 years supervisory experience
• Preferred to have experience or knowledge of manufacturing and/or transfusion operations
• Must maintain knowledge of regulatory requirements concerning validation, calibration, quality control, and maintenance of equipment and supplies used at Oklahoma Blood Institute
• Must maintain knowledge of and perform according to Standard Operating Procedures (SOPs) and policies
• Must have excellent supervisory, planning and organizational skills
• Must have strong leadership skills and professional appearance and demeanor
• Must have excellent written and oral communication skills
• Must be professional, detail oriented, self-motivated, innovative, creative, assertive, organized, communicative, and have the ability to work independently
• Must maintain good working rapport with all departments
• Must be able to make decisions regarding operation and personnel of the department
• Strong computer skills are preferred

Primary Responsibilities:

• Lead validation of instruments, equipment and products
• Lead continual improvement of all manufacturing documentation (SOPs, WIs, TPs) to ensure they are current, accurate, and clear
• Coordinate cost saving measures by working to improve and streamline manufacturing processes
• Direct supervision of Manufacturing CTII, CTIII, Lead Tech, Quarantine Specialist and Coordinator staff
• Work with Shift/Area Leads to provide timely performance feedback, recognizing and rewarding high achievers, and holding personnel accountable for performance in the Component Manufacturing and Quality Control Laboratories
• Oversee scheduling, personnel development, cross training initiatives, and shift change eligibility when applicable
• Assist with the implementation of new or revised tests, procedures, and equipment with SOPs and CFR regulations
• Effectively coach and counsel employees
• Lead containment/escalation of issues and deviations both within manufacturing and to support functions
• Assist Training Coordinator to ensure all techs are trained appropriately and competency is verified annually/semi-annually as required
• Ensure all product discards are complete within 7 days of the end of the month for efficiency in completing the monthly loss reports
• Ensure product reconciliation is performed
• Partner with Shift/Area Lead and Quality Assurance to identify events that are deviations and completes event investigations
• Maintain a safe working environment and report incidents/accidents to Manager of Technical Operations
• Take call as necessary

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