Assistant Manufacturing Associate
- Complete training and demonstrate competency on Assistant Manufacturing Associate qualification blocks in accordance with the training progression pathway
- Execute and document procedural steps in compliance with CGMP standards, clean room behavior and Standard Operating Procedures
- Comply with all applicable rules and regulations of Emergent and the Pharmaceutical / Biotech industry. This includes FDA regulations such as CGMP, GDP, EH&S regulations, and company regulations such as the employee handbook
- Maintain state of facility environmental control including preparation of defined concentrations of cleaning solutions, daily, monthly, quarterly, and annual cleaning of manufacturing areas per Standard Operating Procedures
- Review all documentation for accuracy and completeness of process signature steps as each step is completed. Perform “real time” review of all documentation (BPRs, forms, logs, etc.) in the area throughout the shift
- Stock gowning and consumable supplies in the controlled areas maintaining Kanban inventory control of manufacturing materials
- Follow standard work guidelines
- Collaborate with applicable Integrated Process Teams to participate in continuous improvement and learn new Lean concepts
- Actively participate in Kanban and 6S programs
- Successfully complete inspector qualification requirements to identify, classify and cull product defects, including those defects which could impact patient safety (inspector qualification)
- Independently operate labeling equipment with minimal supervision (Qualification)
- Apply traceability and expiration information to secondary packaging components such as cartons and cases. Confirm suitability of secondary packaging components during printing processes through 100% inspection (carton printing, case creation)
- Package product in secondary and final packaging components while performing 100% reconciliation of product rejects (Packaging)
- Complete ambient tracking documentation
- Execute material issuance and confirmation of process steps using specific SAP modules
- Execute material issuance and confirmation of process steps using specific SAP modules
- Precisely weigh and hydrate media components
- Load, run and unload parts washer and sterilization/decontamination using specific validated load configurations per Standard Operating Procedures
- Assemble clean process glassware configurations and portable tanks utilizing sanitary connections, quick connects and stainless-steel ancillary parts
- Perform Cleaning (COP/CIP) and Sterilizing (SOP/SIP) of production vessels through interface with automated control system (DeltaV)
- Prepare and dispense intermediate materials.
- Standing Shoulder to Shoulder (no matter what):
- working collaboratively with others, communicating, and managing conflict effectively
- Break Through Thinking:
- cultivating innovation and nimble learning
- Own It Always:
- ensuring accountability, and making good and timely decisions
- Compete Where It Counts:
- demonstrating courage and focusing on customers
- Integrity and Instills Trust:
- gaining the confidence and trust of others through honesty, integrity and authenticity
- Manages Complexity:
- making sense of complex, high quantity, and sometimes contradictory information to effectively solve problem
- Plans and Aligns:
- plan and prioritize work to meet commitments aligned with organizational goals
- Drives Engagement:
- creating a climate where people are motivated to do their best to help the organization achieve its objectives
- HS Diploma
- 0–1-year experience working in a CGMP environment
- Knowledge of CGMP and CFR requirements preferred but not required
- Personal Competencies: Self-awareness, Integrity, Team Player, Creative, and Culturally aware
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