Valeant Pharmaceuticals

Sr. Technician (Technician V)

US-CA-Irvine
Job ID
8546
Category
R&D
Pos. Type
Full Time

Overview

Job Title: Sr. Service Technician - Technician V

 

Pay Band: 42

 

 Shift: 1st

 

Hours: Monday – Friday 8:00am – 5:00pm

Responsibilities

The Senior Service Technician is responsible for providing testing support for development of new and existing medical device products such as IOLs and injectors. Must work independently with limited direct supervision from the R&D engineers. Perform lab work as per general written/verbal instructions for routine work and detailed instructions on new work.

 

Specific Duties

  • Executes engineering tests and DOE studies to support design and development of new products.
  • Provides input into product design, testing, and processes.
  • Supports root cause investigations and corrective action activities to address product performance issues.
  • Keeps complete and accurate documentation of all work and summarize data for reporting to the engineers.
  • Recognizes problems and takes corrective actives as needed.
  • Follows Protocols to execute Validation studies to support regulatory submission in global markets.
  • Assume leadership responsibilities organizing test material for evaluation, checking completeness of work and organizing work assignments.
  • Requisition material and supplies necessary for the work to be done.
  • As needed, participates in project team meetings & provide written and verbal updates.
  • Maintains safety and environmental regulations in the lab.
  • Ensures product quality and perform all tasks in accordance with established SOPs, GMP and Divisional Specifications.
  • Reports progress and other concerns on a regular basis.
  • Performs other duties as assigned.

Qualifications

Experience: Minimum 10 years’ experience. Medical device experience preferred. Experience in ophthalmic medical device industry is a plus.

 

Qualifications

  • Associates degree or equivalent specialized training required.
  • Ability to communicate and work in project teams.
  • Ability to work without close supervision.
  • Ability to complete assignments as requested.
  • Ability to create technical documents and packages (procedures and transfer packages).
  • Ability to work in a FDA regulated, clean room manufacturing environment of medical devices.
  • Strong interpersonal skills in combination with solid communication skills.
  • Strong hands-on mechanical/computing aptitude and troubleshooting skills.
  • Strong documentation skills suitable to working in a project-based global team and communicating/coordinating with outside suppliers as well.
  • Ability to read and understand engineering drawings.
  • General computer skills including Word and Excel.

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