Medical Device Tech - Inspection & Fulfillment

ADP, Inc.; Belgrade (MT); On-site; USD 25,000 - 30,000; Full time

Job summary

Xtant Medical seeks a Medical Device Tech to perform inventory fulfillment, quality maintenance, and regulatory tasks in Belgrade, MT. You will support the Medical Device Technician Team Lead and work to meet FDA/ISO standards.

The role emphasizes GMP, GDP, safety procedures, and accurate documentation while handling trays, inventory, and product inspections. Strong detail orientation and ERP proficiency are essential.

Qualifications

• High School Diploma or equivalent required.
• Experience with ISO 13485 QA and cGMP preferred.
• Experience with inventory control software.
• 1 year of QA/manufacturing experience preferred.
• ERP experience is highly desirable.

Responsibilities

• Perform inventory fulfillment and quality maintenance activities.
• Ensure FDA/ISO compliance and maintain necessary documentation.
• Adhere to GDP, GDP and safety SOPs during processing and packaging.
• Support product inspections and packaging operations.
• Assist with tracing, lot control and traceability in ERP system.

Skills

Quality control

Inventory control

Regulatory compliance

Attention to detail

ISO 13485 knowledge

Education

High School Diploma

Tools

ERP software

Job description

Medical Device Tech - Inspection & Fulfillment

Full Time Technical Belgrade, MT, US

3 days ago Requisition ID: 1213

Salary Range: $20.00 To $20.00 Hourly

Classification: Full Time - Non-exempt

Reports to: Medical Device Technician Team Lead

• Job Summary

This position will perform activities related to inventory fulfillment, quality maintenance, and regulatory compliance in their department, as assigned. This person will support the activities of the Medical Device Technician Team Lead and/or Manager.

This position works with the department team lead and manager and with other technicians at the fulfillment and distribution level to help ensure that Xtant Medical complies with and meets the standards of theFood and Drug Administration (FDA) and International Organization of Standardization (ISO), and other regulatory agencies as necessary in distributing Xtant Medical inventory.

• Supervisory Responsibilities
  • This position does not supervise others or teams
• Duties and Responsibilities
  • Develop and maintain an understanding of relevant industry standards and regulations including but not limited to 21 CFR 820, 21 CFR 1271, AATB, MDSAP (per jurisdictional requirements), and ISO 13485, ensuring compliance with these requirements across the organization.
  • Actively contribute to the fulfillment of Xtant Medical’s mission, values and quality policy
  • Maintain a safe, clean work environment and ensure proper disposal of hazardous and non-hazardous waste according to OSHA guidelines and Xtant Medical standard operating procedures (SOP)
  • Develop and maintain an understanding of Xtant Medical products
  • Understand the interaction of departmental activities with the Quality System and their impact on the production of medical devices and human cells, tissues, and cellular and tissue-based products (HCT/Ps)
  • Adhere to Xtant Medical SOPs, Good Documentation Practices (GDP), and safety protocols
  • Perform Quality Control (QC) as required by SOPs
  • Assist with managing inventory warehouse counts utilizing cycle count program
  • Follow OSHA bloodborne pathogen standards, universal precautions, AATB Standards, and current Good Manufacturing Practices (cGMP), and current Good Tissue Practices (cGTP) during all phases of processing packaging, storage and cleaning
  • Daily Product Transaction Activities – inventory allocation within an ERP system, tracking and reconciling inventory returns to match finance and invoicing
  • Maintaining tray inspection throughput to provide necessary inventory redistribution within a timely manner
  • Receiving/Inspecting/Reprocessing of Surgical Sets and Reconciling Associated Documentation
  • Building of Sets for Product Launches and Reconciling Associated Documentation
  • Identifying Material Storage & Stock Locations
  • Track Material with Limited Shelf Life or Expiration Dates to appropriately discard inventory if within expiration window
  • Processing of returned trays from field:
    • Allocate new inventory from warehouse to fill empty tray items
    • Transfer items missing in tray to Distributor’s MIA warehouse for invoicing
    • Update lot numbers in all trays to properly track inventory
    • Complete all associated documentation and tray second checks before returning to finished goods shelf
    • Report missing inventory items to invoicing to verify billing and transact records
  • Other duties as assigned
• Submit timely expense reports and abide by the Expense Reimbursement Policy
• Training
  • Complete required training, including but not limited to initial orientation and environmental health and safety training prior to performing tasks
  • Participate in training programs, ensuring timely completion and accurate, up-to-date training records
  • Complete annual SOP review and safety training (i.e. OSHA, bloodborne pathogens) as applicable
  • May require OSHA (bloodborne pathogen) training, SDS, and other safety training as applicable
  • May be asked to travel to complete LIVE training and job shadowing
• Document Control and Record Control
  • Complete all documentation accurately and legibly per GDP, retain records according to Xtant Medical’s procedures, and review others’ documentation as needed
• Performance of Duties
  • Perform duties and responsibilities to the highest standards with efficiency, professionalism, and attention to detail; adapt to job changes and contribute to team success
  • Represent the company in a professional manner to the public, customers, and vendors and maintain trusting relationships with physician partners, customers, and fellow employees
  • Maintain confidentiality of donor and recipient information according to HIPAA
• Required Skills/Abilities
  • Must be able to reason independently and work with guidance
  • Professionalism and strong communication skills
  • Attention to detail and quality control
  • Basic knowledge of ISO 13485 Medical Devices – Quality Management System and FDA 21 CRF Part 820 Quality System Regulation
  • Experience with manufacturing related Inventory Control software
  • Ability to manage multiple tasks but maintain focus to finish job to completion
  • Effectively utilize PC applications to complete required job function
  • Understands sense of urgency in a fast-paced environment but commits to quality over quantity
  • Ability to interpret data and make sound judgments based on those interpretations
  • Must be able to adapt to quickly changing priorities and schedules
  • Must have excellent manual dexterity and good eye/hand/foot coordination
• Education & Experience
  • High School Diploma or equivalent is required
  • Basic knowledge of ISO 13485 Medical Devices – Quality Management System and FDA 21 CRF Part 820 Quality System Regulation
  • Experience with manufacturing related Inventory Control software
  • 1-year of experience in QA functions and/or manufacturing is preferred, but not required
  • ERP and automated document control experience is desired
• Working Conditions
  • This position is based in an office environment
  • Standard work hours are Monday – Friday; 8:00 am – 5:00 pm, with occasional overtime or weekend work based on project/production needs. Shift times may change based on the current needs of the department
  • This position is located at 732 Cruiser Lane – Belgrade, MT
  • Will operate magnification and inspection/laboratory equipment
  • Duties may include contact with human tissue, blood, bone, and fluids (Clinical Laboratory, Donor Services, Engineering, Processing, Packaging and Labeling, etc.). Working in PPE such as cleanroom suites, with face shields and masks as necessary
  • Adhere to all health and safety requirements specified when entering laboratory and device manufacturing areas and in the handling of company products
  • This position will sometimes be required to wear personal protective equipment (PPE), including laboratory coat, scrubs, gloves, etc.
  • Hepatitis B vaccine is highly recommended and provided to employees who may have contact with human tissue at no cost to the employee. Any employee who declines a Hepatitis B vaccine will be required to sign a waiver
• Physical Requirements
  • Ability to sit, stand, and work at a computer for prolonged periods
  • Ability to lift, carry, push or pull items of varying weight, typically up to 80 lbs.
  • Ability to move, bend, or twist the body in various ways
  • Ability to perform repetitive motions, such as reaching, grasping, bending, squatting, and stooping
  • Requires hand-eye coordination and manual dexterity for tasks such as typing, using hand tools or equipment, and assembling or handling small components with precision
  • Ability to see clearly, whether with or without corrective lenses
  • Ability to hear and understand safety signals, alarms, and requests in a noisy environment

Note: This Job Description is not designed to include a detailed listing of the activities, duties or responsibilities that may be required of the employee. This job description does not constitute an employment contract, implied or otherwise, and is subject to change by the employer as the needs of the employer and requirements of the job change.

Xtant Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.