Manufacturing Technician

Key Responsibilities

• Perform precision assembly of medical devices using microscopes, micro tools, fixtures, and calibrated equipment.
• Follow detailed work instructions, engineering drawings, and process specifications to ensure all assemblies meet defined tolerances.
• Document all manufacturing activities in batch records, forms, and lab notebooks in compliance with GDP standards.
• Prepare chemical solutions and support chemical and electrical based processes such as cleaning, anodizing, or surface treatments.
• Clean and prepare medical device components using established procedures.
• Maintain and disinfect clean rooms, laminar flow hoods, and controlled environments to support ISO classified operations.
• Operate production equipment such as microscopes, ovens, laser tools, bonding equipment, semiconductor tools, and metrology instruments.
• Perform in process inspections using microscopes, measurement tools, and test equipment to verify conformance to specifications.
• Support equipment maintenance, calibration, and troubleshooting in collaboration with engineering and quality teams.
• Assist in manufacturing prototype or pilot scale components for R&D and process development activities.
• Participate in root cause investigations, nonconformance documentation, and corrective/preventive action activities.
• Identify opportunities for process improvements and contribute to continuous improvement initiatives.
• Perform other duties as assigned to support production and operational needs.

Minimum Qualifications and Education Requirements

• Associate degree or equivalent experience in a technical, scientific, or engineering discipline.
• Minimum of 2 years of experience in medical device, biotech, semiconductor, or other high precision manufacturing environments.
• Demonstrated fine motor skills and manual dexterity for handling micro scale components.
• Strong attention to detail and ability to follow complex, multi step procedures.
• Proficiency with pipettes, laboratory equipment, and basic wet chemistry techniques.
• Proficiency in Microsoft Excel.
• Strong verbal and written communication skills.
• Solid understanding of GDP and documentation practices in regulated environments.

Preferred Qualifications And Skills

• Experience in GMP regulated manufacturing (ISO 13485, 21 CFR Part 820).
• Background in Class II or Class III implantable medical device assembly.
• Experience with aseptic technique, sterile assembly, or cleanroom gowning (ISO 7/8).
• Familiarity with micro fabrication, laser processing, or semiconductor processing.
• Working knowledge engineering principles relevant to manufacturing.
• Familiarity with Lean or Six Sigma principles (e.g., waste reduction, root cause analysis, standard work) and ability to apply them to daily manufacturing tasks.
• Ability to apply critical thinking to troubleshoot process deviations or equipment issues.

• Ability to stand, walk, sit, reach, balance, or stoop for extended periods.
• Fine motor skills and dexterity required for micro assembly and handling delicate components.
• Ability to lift up to 25 lbs.
• Ability to visually inspect small parts under magnification for extended periods.

• Frequent work in clean rooms and controlled environments, often in close proximity to others.
• Work in laboratory hoods where fumes or chemical vapors may be present.
• Exposure to hazardous or toxic chemicals with required PPE.

Salary Range: $75,000 - 95,000
Final compensation will be determined based on job‑related factors such as experience, education, and training.

• Medical
• Dental and Vision
• Flexible Spending Account (FSA)
• 401K with Company Safe Harbor Match: 100% /up to 4%
• Life Insurance
• Long Term Disability
• Home Office Stipend
• Commuter benefits