Manufacturing Operator in a 3‑shift production environment, operating and supervising injection moulding or assembly lines, troubleshooting, documenting processes, and contributing to continuous improvement.
Responsibilities
Operate injection moulding or assembly lines
Identify and report product and process deviations
Resolve operational disturbances
Document processes and relevant events
Participate in continuous improvement (KVP) and 5S activities
Supports site operations with on-the-floor QA activities, including area clearances, room changeovers, batch record review, deviation identification, and Veeva workflows.
Responsibilities
Supports site operations with on-the-floor QA activities
Quality Technician responsible for maintaining GMP compliance, conducting inspections, documenting findings, and supporting continuous improvement at the Green Dragon Palatka facility.
Compensation
Compensation: $18/hour
Responsibilities
Work with all teams to maintain compliance with written standards and GMP
Uphold and maintain PPE in each controlled environment
Monitor production processes to identify areas for improvement and implement corrective actions
Perform inspections and tests on products to ensure compliance with quality standards and specifications
Document and report findings from inspections and tests, including any deviations or non-conformities
The Packing Operator will follow direction of the Line Leader and Supervisor, and will perform solid oral dose bottle and/or blister packaging activities.
Responsibilities
Performs routing checks to ensure that the quality standards are met and that no violations to cGMP's occur during the operation of assigned machines.
Takes the initiative, to set the slat pattern and efficiently operate the filling machine at the required speed.
Able to disassemble the Slat Filler, clean the parts, and re-assemble the Slat Filler machine.
Loads and efficiently operates the MGS Topserter at the required speed.
Changes labels on the Labeler and efficiently operates Labeler at the required speeds.
The Receiving and Distribution Lead coordinates complex Blood Typing Solutions shipments including the management of shipments from GDS San Diego to multiple destinations, while handling and storing of materials, parts, supplies, and equipment.
Compensation
The estimated pay scale for Receiving and Distribution Lead based in San Diego, CA, is $29-$38 per hour.
Responsibilities
Oversee and execute the loading, unloading, inspection, and verification of inbound materials (ambient, refrigerated, frozen, and hazardous) against purchase orders and specifications.
Log received items accurately into the warehouse management or ERP system and resolve any discrepancies.
Maintain accurate stock levels through cycle counts, reconciliations, and proper stock rotation (FIFO/FEFO).
Oversee timely distribution of supplies, raw materials, and consumables to internal departments to ensure uninterrupted operations.
Monitor warehouse activities to ensure tasks are completed accurately, efficiently, and safely.
Requirements
High school diploma
Nice to have: international shipping experience (Latin America, Brazil)
The Packing Operator will follow direction of the Line Leader and Supervisor, and will perform solid oral dose bottle and/or blister packaging activities.
Responsibilities
Performs routing checks to ensure that the quality standards are met and that no violations to cGMP's occur during the operation of assigned machines.
Takes the initiative, to set the slat pattern and efficiently operate the filling machine at the required speed.
Able to disassemble the Slat Filler, clean the parts, and re-assemble the Slat Filler machine.
Loads and efficiently operates the MGS Topserter at the required speed.
Changes labels on the Labeler and efficiently operates Labeler at the required speeds.
Lonza is seeking Bioprocess Engineers with a relevant background in Life Sciences and a passion for Biotechnology for Upstream Processing, Downstream Processing or BioConjugate Manufacturing.
Responsibilities
Ensure operational activities for clinical and/ commercial manufacturing are performed on-time and within given safety and quality standards
Act as the functional lead for preparation, manufacturing execution, cleaning and changeover in the assigned area
Lead one or more defined USP areas (e.g. seed train, main cultivation or harvest) for the production of therapeutic proteins with either mammalian or microbial expressions systems
In charge of one or more defined DSP areas (e.g. capture, polishing or filling) for the purification of therapeutic proteins from either mammalian or microbial cells
Responsible for entire processes or process units for clinical and commercial manufacturing projects regarding therapeutic BioConjugates like Antibody Drug Conjugates (ADC)
The Manufacturing Associate II is responsible for operating production equipment, interpreting instructions, checking product quality, maintaining equipment, and troubleshooting minor production problems.
Compensation
Annual base salary for new hires in this position ranges: $53,550.00 - $75,600.00
Responsibilities
Operate manufacturing equipment and machinery to produce high-quality products
Follow standard operating procedures to ensure safety and efficiency in the production process
Perform quality checks on finished products to maintain high standards of quality control
Collaborate with team members to troubleshoot issues and optimize production processes
Maintain a clean and organized work environment to uphold regulatory standards
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