Clean Room Decontamination Technician — Medical Devices

Hologic, Inc.; Marlborough (MA); On-site; USD 45,000 - 68,000; Full time

Job summary

Hologic, Inc. in Marlborough, MA is seeking a Manufacturing Supervisor to oversee decontamination, testing, and assembly in a regulated medical device environment. You will ensure compliance with GMP, ISO 13485, and FDA requirements while leading a cross-functional team.

The role requires a High School Diploma, a technical Electronics credential is preferred, and at least 3 years of manufacturing experience in regulated settings. Strong documentation and communication skills are essential.

Qualifications

• High School Diploma or equivalent required.
• Technical degree or trade certification in Electronics Technology or related discipline preferred.
• Equivalent combination of education and relevant work experience will be considered.

Responsibilities

• Operate decontamination equipment for returned products.
• Clean and decontaminate products using proper PPE.
• Inspect, test, rework, and assemble products and subassemblies.
• Communicate production priorities with cross-functional teams.
• Support process validations and continuous improvement initiatives.
• Maintain 6S workplace standards and clean, safe environment.
• Verify calibration status and equipment readiness.
• Perform routine and preventive maintenance on equipment.
• Complete GMP-compliant manufacturing records accurately.
• Work effectively in a team-based manufacturing setting.
• Operate in Clean Room environments when required.
• Follow safety, quality requirements and company policies.
• Support special projects and overtime as needed.

Skills

MS Office

ERP/MRP systems

Oracle

Agile

Documentation

Communication

Education

High School Diploma

Electronics certificate/Technical degree

Experience considered

Tools

Oscilloscopes

Multimeters

Calibrated equipment

Job description

Hologic, Inc. in Marlborough, MA is seeking a Manufacturing Supervisor to oversee decontamination, testing, and assembly in a regulated medical device environment. You will ensure compliance with GMP, ISO 13485, and FDA requirements while leading a cross-functional team.

The role requires a High School Diploma, a technical Electronics credential is preferred, and at least 3 years of manufacturing experience in regulated settings. Strong documentation and communication skills are essential.