Manufacturing Assembler II at Verathon
Burnaby, BC, Canada -
Full Time


Start Date

Immediate

Expiry Date

23 Jul, 25

Salary

18.18

Posted On

23 Apr, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Manufacturing Principles, Manual Dexterity, Communication Skills

Industry

Pharmaceuticals

Description

Company Overview:
Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility. Two areas where Verathon has significantly impacted patient care, and become the market leader in each, are bladder volume measurement and airway management. The company’s BladderScan portable ultrasound and GlideScope video laryngoscopy & bronchoscopy systems effectively address unmet needs for healthcare providers and meaningfully raise the standard of care for patients. Verathon, a subsidiary of Roper Technologies, is headquartered in Bothell, Washington, USA and has international subsidiaries in Canada, Europe and Asia Pacific. For more information, please visit www.verathon.com.
Overview:
Verathon® is looking for a Manufacturing Assembler II to become the newest member of our Operations located in Burnaby, British Columbia.

Responsibilities:

  • Assemble, test and rework electronic devices utilizing approved procedures
  • Maintain proper documentation to meet quality regulations
  • Ensure that daily production and quality targets are met
  • Maintain a clean and safe work environment
  • Responsible for learning new assignments quickly and effectively
  • Assist with the training of new and current co-workers on procedures
  • Uphold Verathon’s Company Mission and Culture Statement
  • Ensure consistent professional communication with all team members
  • Work on ad-hoc projects when required
  • Support Verathon’s Quality Management System that establishes and maintains effective quality assurance processes and compliance to the International Standards: ISO13485, Canadian Medical Device Regulations (CMDR, SOR 98-292), FDA Quality System Regulations (QSR, 21 CFR Part 820) and the Medical Device Directive (MDD93/42/EEC)

Qualifications:

  • 2 – 3 years of intermediate to senior manufacturing experience in electro-mechanical industry preferred
  • Excellent manual dexterity and hand-eye co-ordination
  • Excellent soldering and mechanical assembly skills
  • Ability to read and interpret procedures and drawings
  • Strong interpersonal communication skills
  • Understanding of Lean Manufacturing principles
  • Attention to detail, ability to meet deadlines and work under time demands
  • Ability to ensure that daily production and quality targets are met
Responsibilities
  • Assemble, test and rework electronic devices utilizing approved procedures
  • Maintain proper documentation to meet quality regulations
  • Ensure that daily production and quality targets are met
  • Maintain a clean and safe work environment
  • Responsible for learning new assignments quickly and effectively
  • Assist with the training of new and current co-workers on procedures
  • Uphold Verathon’s Company Mission and Culture Statement
  • Ensure consistent professional communication with all team members
  • Work on ad-hoc projects when required
  • Support Verathon’s Quality Management System that establishes and maintains effective quality assurance processes and compliance to the International Standards: ISO13485, Canadian Medical Device Regulations (CMDR, SOR 98-292), FDA Quality System Regulations (QSR, 21 CFR Part 820) and the Medical Device Directive (MDD93/42/EEC
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