Mechanical Technician Ii - Sylmar, United States - Validation Associates

Validation Associates
Validation Associates
Verified Company
Sylmar, United States

3 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description

Description:


  • Performs research and engineering functions involving the layout, building, testing, troubleshooting, repairing and modification of, but not limited to, cardiac lead assemblies and implantable medical devices.
  • Performs a variety of duties in the electrical, mechanical, electromechanical, chemical, or optical areas.
  • Constructs, operates, troubleshoots, calibrates, adjusts, maintains, and tests equipment, systems, or products.
  • Works from schematics, engineering drawings, and written or verbal instructions.
  • Performs tests, analyzes data, and writes reports.
  • Reviews and/or develops processing and/or manufacturing instructions.
  • Maintains detailed documentation through all phases of development, testing and analysis.
  • Plans and organizes nonroutine tasks with approval.
  • Initiates or maintains build/project schedule and establishes priorities of work assignments with management input.
  • Solves a wide range of problems requiring some interpretation of defined procedures and practices.
  • Selects methods and practices with guidance from supervisor to obtain imaginative, thorough, and practical solutions to questions.
  • Maintains general knowledge of products/services associated with area and employees involved with specific product lines and services.
  • Validate components and fixtures following receiving inspection standard procedures.

Qualifications:


  • H.S. diploma or equivalent.
  • 35 years of medical device (or similar field) manufacturing/assembly experience and/or 2+ years of experience in technician trade or equivalent technician experience.
  • Receive general instructions and able to work independently and efficiently without direct guidance, solve challenges, and appropriately relay concerns to management when needed.
  • Exercises judgment within defined procedures and practices to determine appropriate action.
  • Understands timelines and ensures deadlines are met with high quality work. Responsible for completing project tasks successfully within time and budget constraints.
  • Perform routine and nonroutine moderately complex assignments using standard methods and sequences.
  • Assignments require broad judgment in troubleshooting proven processes as well as the ability to suggest alternatives.
  • Work in a stringent quality system environment. Work experience in the medical industry under FDA regulation preferred.
  • Good communication skills, both written and verbal required.
  • Interacts well with diverse groups and maintains strong working relationships with internals in a collaborative, fastpaced, goaldriven environment.
  • Listens to and understands others' points of view; possesses interpersonal skills to negotiate and reconcile differences.
  • Exercises discretion regarding work details.
  • Coordinates efforts with technical and support staff.
  • Ability to utilize a SmartScope or other CMM a plus.
  • Experience with validating raw materials, parts, or components through receiving inspection a plus.

Job Type:
Contract


Pay:
Up to $31.00 per hour


Schedule:

  • 8 hour shift

Experience:

- medical devices: 2 years (required)

- troubleshooting: 2 years (required)


Work Location:
On the road
More jobs from Validation Associates
See all jobs of Validation Associates