Weekend Medical Device Assembler (GMP & QC)

Employbridge; Maple Grove (MN); On-site; USD 25,000 - 30,000; Part time

Job summary

EmployBridge is seeking detail-oriented Medical Assemblers to join our Maple Grove manufacturing team. This weekend opportunity is ideal for individuals who enjoy working with small components in a clean, regulated production environment and are comfortable using computers as part of their daily responsibilities.

Responsibilities include assembling components, performing inspections, documenting activities in computer systems, and maintaining GMP-compliant processes while meeting production

Qualifications

• Ability to work with small components and perform detailed assembly tasks.
• Basic computer skills and comfort navigating electronic systems.
• Strong attention to detail and hand-eye coordination.
• Ability to follow written instructions and standard operating procedures.
• Previous manufacturing, assembly, medical device, or GMP experience is a plus but not required.
• Ability to sit or stand for extended periods and perform repetitive tasks.

Responsibilities

• Assemble small medical device components according to work instructions and quality standards.
• Perform visual inspections to ensure product quality and compliance.
• Accurately document production activities using computer-based systems.
• Follow GMP regulations and company procedures.
• Maintain a clean and organized work area.
• Meet production goals while adhering to safety and quality requirements.

Skills

Small components handling

Attention to detail

Basic computer skills

Follow SOPs

GMP awareness

Tools

Computer systems

Job description

EmployBridge is seeking detail-oriented Medical Assemblers to join our Maple Grove manufacturing team. This weekend opportunity is ideal for individuals who enjoy working with small components in a clean, regulated production environment and are comfortable using computers as part of their daily responsibilities.

Responsibilities include assembling components, performing inspections, documenting activities in computer systems, and maintaining GMP-compliant processes while meeting production