Manufacturing Support Associate 3
- Lead operational readiness initiatives to prepare people, processes, equipment, and systems for start-up.
- Lead site commissioning and qualification efforts to ensure facilities and equipment are ready for compliant use.
- Lead troubleshooting in assigned process areas, acting as a process subject matter expert to resolve issues, prevent recurrence, and minimize downtime.
- Coordinate batch planning, including creating process templates and importing and managing preventive maintenance plans.
- Recommend and perform documentation updates to keep records accurate, current, and aligned with process improvements.
- Initiate and support training and onboarding; develop, manage, and improve curricula that build consistent capability across shifts.
- Coordinate non-batch activities and create associated documentation for changeovers, preventive maintenance, and column packing.
- Support technology transfer, ensuring seamless introduction and scale-up of processes within manufacturing.
- Initiate or support change management records, investigations, corrective and preventive actions, and continuous improvement activities.
- Identify and drive highly technical improvement projects in drug substance manufacturing to enhance reliability, yield, and throughput.
- Support inspections and audits by preparing and providing required manufacturing documents and evidence of compliance.
- Perform other duties, as assigned, to meet production, quality, and safety goals.
- Operate advanced machinery used in production, including assembly lines, presses, and related equipment, to meet quality standards and production targets.
- Set up and fine-tune machines, monitor production processes, and troubleshoot moderately complex technical issues; promptly alert colleagues of more complex issues or suspected faults.
- Maintain accurate, timely production records and strictly follow all safety regulations and procedures.
- Expertise in manufacturing operations with a high degree of troubleshooting ability.
- Strong technical experience with batch planning and the creation and maintenance of manufacturing documentation.
- Experience supporting audits, leading investigation support activities, and leading continuous improvement projects.
- Clear communicator with strong collaboration skills across operations, quality, and engineering.
- Organized, detail-focused, and able to prioritize in a dynamic, around-the-clock environment.
- High School Diploma with 8 years of related experience; or
- Associate's Degree with 6 years of direct experience; or
- Bachelor's Degree with 4 years of direct experience; or
- Equivalent military experience or training
- Associate's or Bachelor's Degree, preferably in life sciences or engineering
- BioWorks or BTEC Capstone current Good Manufacturing Practice coursework preferred
- High-impact ownership: Lead readiness, troubleshooting, and continuous improvement that directly affects delivery and quality.
- Technical growth: Build depth as a process expert while shaping training and documentation that scale best practices across shifts.
- Team culture: Partner with skilled colleagues committed to safety, compliance, and operational excellence.
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