Manufacturing Technician (1st and 2nd shift)

Page Mechanical Group, Inc.; North Wilmington (MA); On-site; USD 40,000 - 70,000; Full time

Job summary

A leading company in medical device manufacturing is seeking a Manufacturing Technician. This role involves operating production equipment and maintaining quality for restor3d implants and components. Ideal candidates should have a high school diploma and experience in regulated environments, with strong organizational and communication skills.

Qualifications

• Experience in a medical device or regulated environment preferred.
• Familiarity with ISO Standards and Good Manufacturing Practices.
• Demonstrated English reading and writing skills.

Responsibilities

• Operate production equipment while maintaining quality.
• Perform machine set-ups and execute maintenance tasks.
• Adhere to Good Documentation Practices during all tasks.

Skills

Communication

Organizational skills

Analytical skills

Time-management skills

Education

High School Diploma or GED

Tools

Oracle ERP

Microsoft Office

Job description

Job Summary:
The Manufacturing Technician position is responsible for operating production equipment in a productive manner while maintaining a high level of quality in the manufacturing of restor3d implants and components.

1^stShift – Mon – Fri, 7:00am – 3:30pm

2nd Shift - Monday - Fri, 3:30 pm - 11:30 pm

Essential Duties and Responsibilities:

• Develop and maintain strong, internal working relationships across restor3d.
• Understand the objectives, responsibilities, and mission of the Manufacturing department and works towards those goals.
• Prioritize and plan work activities; adapt for changing conditions.
• Execute daily maintenance and start-up activities.
• Perform machine set-ups.
• Operate machinery and processing equipment, including but not limited to clean line and pouch sealers, Perform inspection of components and assembly as required.
• Perform cleaning, pouching/sealing and labeling
• Strict adherence to Good Documentation Practices when executing all assignments.
• Perform timely and accurate transactions of workflow in ERP system.
• Participate in inventory cycle counts, variance investigation and reconciliation.
• Assist in the investigation and implementation of corrective actions on product and process failures.
• Comply with all company policies and procedures including safety regulations, personal protective equipment requirements, Standard Operating Procedures, Work Instructions and Good Manufacturing Procedures.
• Responsible for upkeep of manufacturing areas and provide a clean and safe work environment.
• Review all manufacturing documentation, assembly, inspection, test, packaging procedures and provide feedback.
• Other duties as assigned.

Qualifications:

• High School Diploma, GED, or equivalent work experience; work experience in a medical device and/or regulated environment preferred
• Familiarity with Oracle (or equivalent) ERP systems and Microsoft Office Applications
• Familiar with ISO Standards and Good Manufacturing Practices
• Good verbal and written communication
• Demonstrated English reading and writing skills
• Shipping/receiving/stockroom experience a plus.

Skills, Abilities, Competencies Required:

• Good written and verbal communication skills.
• Demonstrated ability to monitor own work to ensure quality, accuracy and thoroughness.
• Strong organizational, analytical and time-management skills.
• Able to self-motivate and work both independently and as part of a team.
• Manual dexterity to handle tools, inspection gauges and equipment of different sizes.
• Demonstrated organizational skills.
• Ability to work in a fast-paced environment and multitask. Comfortable with change.
• Ability to work as part of a team as well as independently.

Working conditions:

• Ability to lift, pull and push up to 40 lbs
• Ability to stand for prolonged periods of time
• Ability to work in a Class 10,000 or ISO class VII clean room environment for prolonged periods of time
• Busy work environment with frequent interruptions
• Flexible to work overtime, extended hours and weekends as business demands
• Must be aware of hazards within the company; adhere to quality and safety standards established by FDA and other regulatory agencies
• Able to work in changing environments (reduced lighting, increased noise, temperature variances, unpleasant odors, dust etc.).