Manufacturing Technician 2

Under general supervision, perform assembly, testing, inspection, calibration, troubleshooting, rework, and repair of products, equipment, and subassemblies in accordance with approved assembly drawings, schematics, work instructions, and quality procedures. Ensure compliance with applicable quality system and regulatory requirements, including ISO 13485, FDA Quality System Regulations (21 CFR Part 820), and GMP standards.

The responsibilities listed below are representative of the essential functions of this position. Additional duties may be assigned as required to support business needs.

• →Assemble, test, calibrate, troubleshoot, and repair production equipment, products, and subassemblies according to specifications and established procedures.
• →Accurately document test results, process data, and production records in accordance with quality and regulatory requirements.
• →Partner with Engineering, Quality, and Operations teams to support production objectives and continuous improvement initiatives.
• →Maintain and communicate daily production metrics through management board updates.
• →Participate in process validation activities and recommend improvements to enhance quality, efficiency, and productivity.
• →Adhere to 6S standards and maintain a safe, clean, and organized work environment.
• →Perform inventory transactions and maintain accurate inventory records.
• →Verify that all calibrated equipment is operating within specified limits prior to use.
• →Review nonconforming material documentation for completeness and accuracy.
• →Report product, process, or equipment issues through the Nonconformance Report (NCR) process.
• →Work effectively both independently and as part of a team.
• →Perform work in a controlled manufacturing or clean room environment as required.
• →Complete routine equipment maintenance and assist with troubleshooting activities.
• →Follow all safety procedures, GMP requirements, and company policies.
• →Support special projects and cross-functional initiatives as assigned.
• →Work overtime as needed to meet production schedules and business demands.

• Must comply with all applicable FDA regulations, ISO requirements, and company quality standards.
• Must be able to work in a manufacturing environment and perform duties requiring standing, walking, lifting, and manual dexterity as needed.
• Ability to work overtime as necessary to support production requirements.

• High School Diploma, GED, or equivalent required.
• Technical degree or trade school certification in Electronics Technology, Manufacturing Technology, or a related field preferred.

• Minimum of 3 years of manufacturing experience, preferably in a regulated environment.
• Experience with product assembly, testing, troubleshooting, inspection, and shipping activities.
• Experience in the medical device, diagnostics, electronics, or other highly regulated manufacturing industries preferred.

• Knowledge of Electrostatic Discharge (ESD) practices preferred.
• Proficiency with Microsoft Office applications; experience with Oracle, Agile, or similar ERP/MRP systems preferred.
• Experience using hand tools and test equipment, including screwdrivers, wrenches, torque tools, crimpers, soldering equipment, multimeters, and oscilloscopes.
• Ability to read and interpret assembly drawings, schematics, specifications, and work instructions.
• Understanding of GMP, FDA regulations, and ISO 13485 quality system requirements.
• Strong computer skills, including data entry, documentation, and spreadsheet applications.
• Effective verbal and written communication skills.
• Ability to work independently with minimal supervision while maintaining high-quality standards.
• Strong attention to detail, accuracy, and organizational skills.
• Demonstrated commitment to continuous improvement and operational excellence.

Agencies that submit resumes to Hologic must have a current, fully executed Hologic Agency Agreement approved by the Human Resources Department. Agencies may only submit candidates for positions when specifically authorized by a Hologic Recruiter. Resumes submitted outside of these terms will not be considered.

Hologic is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

This position must comply with all applicable FDA regulations and ISO requirements.