Facilities Mechanic

Dendreon Corporation•Seal Beach, CA

3d•$25 - $32•Onsite

About The Position

The Facilities Mechanic I is an integral member of a team responsible for assisting and performing building maintenance, equipment maintenance and metrology work for a cGMP compliant pharmaceutical research facility. In addition, this position will train to back-up their direct supervisor during vacations or unplanned leave. This position is ideal for a sharp, mature, and responsible self-starter with career aspirations. NOTE: This role requires on-site presence at our Seal Beach, CA location.

Requirements

Associate Degree in a technical discipline preferred.
Experience working within a regulated GMP environment preferred.
1–3 years of general maintenance experience in a laboratory, manufacturing, or regulated environment preferred, or equivalent combination of education, training, and experience.
Experience completing and documenting work orders using CMMS (BMRAM) or equivalent system preferred.
Competent use of MS office applications and ability to learn specialized programs.
Strong attention to detail with excellent written and oral communications skills.
Self-motivated and able to function effectively within a team environment.
Flexibility to take on additional duties and reprioritize as needed.
Ability to sit or stand for extended periods of time.
Intermittent walking to gain access to work areas.
Finger dexterity sufficient to use a computer and to complete paperwork activities.
Vision sufficient to use a computer, to read written materials and to complete paperwork activities.
Ability to gown aseptically for work in a Clean Room environment.
Hearing sufficient to communicate with individuals by telephone and in person.
Duties may require handling chemicals and biological materials.
Limited exposure to (2ºC - 8ºC); (-20ºC); (-75ºC); (-196ºC) areas.
Must be able to regularly lift 10 – 20 lbs, and on occasion up to 50 lbs.
Ability to climb and work off ladders.
Must have the ability to work around laboratories, manufacturing areas, and equipment, with potential exposure to blood, blood products, or OPIM (other potentially infectious materials), while utilizing required personal protective equipment.

Nice To Haves

Associate Degree in a technical discipline
Experience working within a regulated GMP environment
1–3 years of general maintenance experience in a laboratory, manufacturing, or regulated environment, or equivalent combination of education, training, and experience.
Experience completing and documenting work orders using CMMS (BMRAM) or equivalent system

Responsibilities

Participate in activities involving calibration, validation, and metrology in areas such as temperature, pressure and time interval/rotation on incubators, refrigerators, freezers, centrifuges, fume hoods, biosafety cabinets, and other laboratory equipment.
Performs routine building/office maintenance and repair activities.
Assist with coordination between Facilities, vendors and building management to identify and respond to operational requirements.
Assist with the implementation, revision, maintaining and review of company SOPs and policies.
Performs Routine Safety Inspections.
Support internal and external audit activities relating to GMP compliance.
Responsible for completing all assigned compliance training.
Support tracking and reporting of Facility KPI metrics.
Participate on a scheduled 24/7 on-call rotation and ability to get to our site at any hour day or night in a timely manner. The on-call assignment is typically 1 week (7 days) per month.
Manage time appropriately and work with a sense of urgency.
Cross-train to support departmental operational continuity during supervisor absences.