Manufacturing Assembler (Contractor) - Vantage MedTech
Confirmed on the employer's own hiring board on Nov 6, 2026. First seen by Alion on Nov 3, 2026.
Job Title: Manufacturing Assembler (Independent Contractor)
Duration: 6 - 12-months (possibility of extension)
Employment Type: Independent Contractor (1099)
Business Unit: Manufacturing
Location: Olathe, KS
Vantage MedTech provides comprehensive design and manufacturing services, supporting the advancement of medical technologies from concept through to product realization. We develop and manufacture new products for the treatment of heart failure, cancer, stroke, Gene Therapy, COPD, TBI, Atrial Fibrillation, Blood Clots, Brain Surgery, and many more! We are searching for top-tier talent to apply their gifts to making life better for hundreds of thousands of patients worldwide. If this is something you aspire to, we would like to talk with you!
* This engagement is for an independent contractor (1099) providing services to Vantage MedTech for an anticipated period of 6-12 months, with potential for extension based on business needs. Contractors are not employees of Vantage MedTech and are not eligible for company-sponsored benefits.
Services:
- Contractor shall provide Vantage with Manufacturing Assembly Services.
The Manufacturing Assembler is responsible for assembling medical device components, subassemblies, and finished products in accordance with approved work instructions, quality requirements, and regulatory standards. This position plays a critical role in ensuring product quality, reliability, and patient safety while supporting production objectives in a collaborative manufacturing environment.
Scope:
- Assemble medical device components and subassemblies by using hand tools such as torque drivers, screwdrivers, wrenches, and pliers.
- Perform assembly and soldering activities by following detailed work instructions and procedures.
- Maintain a clean, organized and safe work environment.
- Accurately complete production transactions in ERP systems and document required manufacturing data.
- Assist with packing, labeling, and preparing finished goods for shipment.
- Identify and communicate nonconformances to senior technicians, quality personnel, or engineering staff.
- Collaborate with team members to ensure products meet quality and regulatory requirements.
- Follow documented procedures supporting FDA quality regulations, IS 13485 requirements, and internal quality objectives.
- Support continuous improvement initiatives that enhance safety, quality, and efficiency.
- High school diploma or equivalent.
- Previous assembly, soldering, inspection, or manufacturing experience preferred.
- Basic mechanical aptitude and ability to use hand tools.
- Basic computer proficiency, including familiarity with Microsoft Office applications.
- Ability to follow written and verbal instructions with strong attention to detail.
- Ability to work independently and as part of a team.
- Experience in medical device manufacturing or another regulated industry.
- Familiarity with IPC-A-610 and/or IPC J-STD-001 standards.
- Experience with ERP systems and manufacturing documentation.
- Knowledge of Lean Manufacturing principles.
Physical Requirements:
- Ability to sit, stand, and walk for extended periods.
- Ability to perform detailed assembly work requiring visual inspection and fine motor skills.
- Ability to occasionally lift and move materials up to 40 pounds.
- Reasonable accommodation may be made to enable qualified individuals with disabilities to perform essential job functions.