Manufacturing Technician - 3rd Shift
Merrimack Manufacturing · Manchester, NH · 1 mo ago
On-siteManagementFull-time
About the role
Merrimack Manufacturing is a growing medical device manufacturer located in the Manchester Millyard. We are seeking a resourceful Manufacturing Technician to preserve the condition, functionality, and safety of production equipment. The role requires self-sufficiency in performing preventive and reactive maintenance activities on various equipment and machinery, as well as interfacing with multiple teams to ensure clear communication and task progress.
Responsibilities
- Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures
- Utilize small hand tools (both manual and electric), manual presses, assembly fixtures, calibrated instruments, measurement equipment, microscopes, and test fixtures
- Use documentation such as Bill of Materials, product flow charts, work orders, check sheets, visual aids, production reports, and assembly drawings to assemble product and record results
- Perform soldering, fabricating, crimping, mechanical assembly, sealing, ultrasonic welding, bonding and gluing with adhesives, epoxy or RTV
- Kit assemblies using a parts list, scanner, and inventory software as required
- Participate in routine start-up or end-of-day equipment inspections or verifications
- Inspect work throughout the assembly process and communicate any quality or operational issues to appropriate leadership
- Maintain a neat, orderly, and clean work area to ensure efficiency and safety
- Participate in safety programs, meetings, and trainings; bring safety concerns to management
- Participate in continuous improvement activities as part of a cross-functional team
- Meet all quality, quantity, and good manufacturing practices to satisfy customer and Regulatory Affairs requirements
- Read and/or understand operating procedures for specific products where training has been completed
- Show constant attention to detail and immediately inform supervisor of anything out of the ordinary or non-conforming to approved process sheets
- Work with Engineers and line leads to resolve issues and correct procedures to ensure quality and efficiency
- Maintain clean room integrity by using proper attire and adhering to clean room environment practices and procedures as applicable
- Maintain accurate records/documentation related to quality, work in progress, test results, labor (e.g., timecards), and special projects
- Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations
Qualifications and Skills
- Minimum of 2 years hands-on experience in a manufacturing environment
- Experience with assembly, testing, and the documentation of mechanical and electrical devices
- Exceptional interpersonal, verbal, and written communication skills
- Willingness to undertake various tasks and adapt to unexpected situations within a dynamic company environment
- Medical device manufacturing experience preferred
- Working knowledge of medical device regulatory procedures, lean manufacturing, and manufacturing processes preferred
- Good hand-eye coordination and manual dexterity required
- Experience with small parts assembly and ability to work under a microscope
- Proficiency with tools such as tweezers, torque drivers, magnifiers, and microscopes
- Ability to read, write, and speak English
- Comfortable using computers
- Ability to remain in a stationary position 50% of the time
Education
High School Diploma or GED.