Production Technician

Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger.

The Production Technician (Operator III) supports the manufacturing process by ensuring that production jobs are physically, documentally, and systemically complete and consistent prior to transfer to Quality Assurance. The role reviews manufacturing documentation and Job Travelers, reconciles physical material and system records, verifies packaging and identification, supports the resolution of discrepancies and nonconformances, and completes final manufacturing job-closure activities in accordance with applicable procedures and quality requirements.

Join Resonetics and be part of a team that’s redefining medical device manufacturing. If you’re passionate about innovation and thrive in a fast-paced environment, we’d love to hear from you.

1. Review and verify Job Travelers and supporting manufacturing documentation to ensure operations, signatures, revisions, quantities, inspections, and required records are complete and accurate.
2. Reconcile physical material, production documentation, Job Traveler quantities, and Epicor records; investigate discrepancies and complete authorized corrections or adjustments when required.
3. Verify product labels, packaging, seals, material identification, and quantities to ensure integrity, traceability, and consistency with the applicable Job documentation.
4. Review dimensional reports, AQL records, setup documentation, final inspection records, production forms, and other applicable controlled documentation.
5. Identify documentation errors, material discrepancies, and nonconformances; document and follow up on QCBD/App entries, NCR requirements, rework instructions, and required corrections or escalations.
6. Complete final Job-closure activities, including verification that documentation and quantities are reconciled, Epicor is updated, the MFG operation is complete, final labels are prepared and verified, and material is properly packaged and identified.
7. Prepare and organize the completed Job documentation and transfer the material and documentation package to Quality Assurance once the Job meets the required readiness criteria.
8. Support Production personnel in resolving documentation questions, manufacturing-record discrepancies, and system-related issues, coordinating with Production and Quality as needed.

1. High School Diploma or equivalent required.
2. Minimum of 1 year of manufacturing experience; experience in a regulated or medical-device environment is preferred.
3. Basic knowledge of Good Documentation Practices (GDP), traceability, and controlled manufacturing documentation.
4. Basic computer skills, including Microsoft Office and experience working with manufacturing or ERP systems.
5. Ability to read and interpret work instructions, Job Travelers, labels, drawings, inspection records, and manufacturing documentation.
6. Strong attention to detail and the ability to identify documentation, material, quantity, and reconciliation discrepancies.
7. Effective communication and teamwork skills to coordinate with Production and Quality personnel and escalate issues when necessary.

1. Working knowledge of Epicor, including Job information, raw materials, operations, quantities, production records, scrap, and operation completion.
2. Job Traveler and manufacturing-record review, including verification of current document revisions, completed operations, signatures, inspections, quantities, and required comments.
3. Ability to reconcile physical quantities, production forms, Job Traveler information, and Epicor records.
4. Knowledge of manufacturing documentation such as work instructions, master labels, dimensional reports, AQL records, setup documentation, final inspection records, and retain-sample requirements.
5. Material, labeling, and packaging verification, including label integrity and traceability, seals, containers, packaging condition, quantities, and Job identification.
6. Basic knowledge of nonconformance and documentation-control processes, including QCBD/App entries, NCR requirements, rework instructions, corrections, and escalation of unresolved discrepancies.
7. Basic troubleshooting and problem-solving skills for documentation, material, dimensional, system, and process-related discrepancies.

Resonetics offers a comprehensive benefits package designed to support the health, well-being, and financial security of our employees and their families. Benefits include medical, dental, and vision insurance; a 401(k) retirement plan; paid time off (PTO); 10 paid holidays; Flexible Spending Accounts (FSA); life and Accidental Death & Dismemberment (AD&D) insurance; Short-Term Disability (STD) and Long-Term Disability (LTD) insurance; accident, critical illness, and hospital indemnity insurance. Eligibility and benefit offerings may vary based on employment status and applicable plan provisions.