Manufacturing Technician

A leading Biotechnology company is looking for a Manufacturing Technician to join the team for an initial 3 months starting ASAP. You will support the medical device manufacturing operations, with primary focus on downstream production activities e.g. product inspection, kit assembly, packaging, material handling, documentation and general production support.

Client Details

Our client is a groundbreaking Biotechnology company making waves in their specialized field. This is a fast-paced work environment with a strong team of dedicated and driven Manufacturing professionals.

Description

• Perform manual kit assembly, packaging, sealing, and labeling activities in accordance with approved procedures and batch documentation.
• Inspect components, labels, containers, and finished kits for accuracy, completeness, appearance, and proper configuration.
• Verify product identity, quantity, labeling, lot information, and packaging configuration against applicable work instructions and production records.
• Prepare, assemble, and package finished product kits using defined process steps and controlled materials.
• Operate basic production and packaging equipment such as labelers, sealers, shrink-wrap equipment, torque tools, scanners, scales, or other equipment as required.
• Complete production records, logbooks, forms, and electronic transactions accurately, legibly, and contemporaneously.
• Follow line clearance, segregation, and product status control requirements to prevent mix-ups and maintain GMP compliance.
• Identify and escalate discrepancies, damaged materials, documentation errors, equipment issues, or process concerns to supervision.
• Maintain cleanliness, organization, and GMP readiness of the work area.

Profile

• High school diploma, GED, or equivalent.
• Prior experience in GMP, medical device, pharmaceutical, biotechnology, diagnostics, food, or other regulated manufacturing environment.
• Experience with packaging, kitting, labeling, inspection, assembly, or production documentation.
• Familiarity with Good Manufacturing Practices, Good Documentation Practices, line clearance, material reconciliation, or batch record execution.
• Experience using electronic documentation, ERP, inventory, or production tracking systems.
• Basic understanding of metric units and material/component traceability.
• Ability to read, understand, and follow written procedures, batch records, and work instructions.
• Strong attention to detail and ability to perform repetitive manual tasks accurately.
• Ability to speak, read, and write English sufficiently to complete GMP documentation and follow safety instructions.
• Basic math skills, including ability to count, reconcile quantities, and understanding units of measure.
• Ability to work in a controlled manufacturing, laboratory, warehouse, or cleanroom-adjacent environment.

Job Offer

• Hourly rate $20-$25.
• On site in Irvine/Santa Ana, California.
• 2nd shift 1pm - 9:30pm.
• Quick interview process.
• 2 week training period with pass or fail.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.