Facilities Technician II

EvergenEden Prairie, MN
13d$22 - $25Onsite

About The Position

Purpose of this position is to provide support to production operations either directly by assisting with production related activities or indirectly by maintaining and/or introducing new critical building equipment and systems.

Requirements

  • Experience working under an ISO 13485 quality system.
  • Calibration and maintenance experience.
  • Fault finding and resolution.
  • Safe manual handling activities.
  • Escalation of identified issues in a timely manner.
  • Teamwork, Communication & Continuous Improvement mindset.
  • Proficient with Microsoft Office (Word, Excel, Project etc.).
  • Strong organizational and time management skills.
  • Strong ability to demonstrate sound judgement under all circumstances and in a timely manner.
  • Excellent interpersonal and collaborative skills, with a professional demeanor and the ability to interact with all levels of management, colleagues, and vendors.
  • Effective oral and written communication.
  • Validation of new and existing equipment.
  • Detail-oriented.
  • Ability to be self-motivated and to work independently.

Nice To Haves

  • Stock control and management experience preferred.
  • Associate or bachelor’s degree preferred.
  • Experience within Medical Device Industry preferred.

Responsibilities

  • Perform and/or facilitate equipment calibrations and preventative maintenance in accordance with internal procedures on process and/or test equipment and facility plant systems within specific timescales / deadlines to keep calibration and maintenance schedule up to date.
  • Perform plant walk-arounds recording the status of plant equipment and associated systems to aid in preventative maintenance. Data gathering on the performance of equipment.
  • Communicate with other departments to assist in the planning of planned or unplanned maintenance which may affect production or quality.
  • Assist with the control and monitoring of production related materials and critical spares.
  • Liaise with external service providers who visit the site to perform critical works, as required.
  • Execute equipment validations, as assigned, on new and existing equipment including IQ/OQ/PQ to ensure that equipment conforms to required specifications. To include introduction of new equipment and systems for production use.
  • Writing/editing documentation such as work instructions, SOP’s etc as applicable.
  • Assist with waste disposal procedures to ensure the safe and compliant disposal of waste from the site.
  • Participate in Health and Safety initiatives throughout the site.
  • Ensure all activities are performed in accordance with cGMP where applicable, ISO 13485 / ISO 22442 and any other relevant regulations or SOPs. Always keep training folder up to date.
  • Actively support timely closure of CAPAs, Non-conformances, and deviation reports wherever the area of expertise allows

Benefits

  • Benefits including health, dental, vision, PTO, & paid holidays
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