Assembler II

Abbott•Temecula, CA

20d•$16 - $31•Onsite

About The Position

The Assembler II works under close supervision at Abbott Vascular Devices in Temecula, California. The role performs routine, standardized assembly, welding, soldering, x-ray, repair, testing, casting/coating, mechanical assembly, and packaging operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical-device assemblies. Work is closely and continually reviewed, and certain problems may be referred to a supervisor or more senior personnel. The position uses microscopes, applicable tools, production equipment, computerized test equipment, small hand tools, and precision measuring instruments. Work takes place in a production or air-conditioned clean-room manufacturing environment and requires gowning attire. The role supports company initiatives and quality, environmental, and regulatory systems; follows FDA requirements and company policies and procedures; and communicates and collaborates with employees, customers, contractors, and vendors.

Requirements

High school diploma or equivalent.
Typically six or more months of relevant training or experience in assembly of digital or analog circuitry, devices, components, or equivalent.
Demonstrated manual dexterity and hand-eye coordination.
Ability to use standard hand tools used in assembly of bio-instruments or bio-devices.
Ability to work cooperatively and productively with others, multitask, rotate through assigned work-group jobs as needed, and meet deadlines on multiple projects.
Demonstrated spelling, punctuation, grammar, basic math/numerical, and organizational skills, and familiarity with standard manufacturing and office equipment and procedures.
Ability to read, write, and communicate effectively in English, including clear speech and demonstrated comprehension skills.
Successful completion of a mandatory reading-comprehension pre-employment examination.
Ability to understand and comply with applicable FDA regulations and company operating procedures, processes, policies, and rules.
Ability to occasionally lift up to approximately 25 pounds.
Ability to work in a highly matrixed and geographically diverse business environment, both as a team member and an individual contributor, in a fast-paced, changing environment.
Ability to leverage or engage others to accomplish projects.
Strong verbal and written communication skills and ability to communicate effectively at multiple organizational levels.
Strong organizational and follow-up skills, with attention to detail.
Ability to maintain regular and predictable attendance.
Availability for regularly scheduled overtime.

Nice To Haves

Experience working in a broader enterprise or cross-division business-unit model.
Formal training in assembly techniques.
Experience assembling manufactured items in a bio-instruments or bio-devices-related facility.
Prior experience in an air-conditioned clean-room manufacturing environment requiring stringent environmental controls.

Responsibilities

Assemble, weld, solder, and x-ray medical devices and related parts using microscopes and applicable tools.
Inspect x-rays and parts visually to identify and correct problems.
Repair and test units using computerized test equipment.
Inspect devices and assemblies after molding for bubbles, nicks, and excess epoxy; access and remove defects, patch or repair voids, and bake parts to cure epoxy patches.
Kit, assemble, bond, coat, and process medical devices and related parts; inspect and correct problems; and repair devices and components using microscopes and applicable tools.
Kit, assemble, and package devices and related accessories; identify and correct problems; and review device documentation for completeness and accuracy.
Set up or use special test equipment as needed.
Notify the supervisor when supplies or materials need replenishment and report production difficulties that cannot be readily corrected.
Perform other related duties as directed or assigned.
Support company initiatives and quality management, environmental management, and other regulatory requirements.
Comply with FDA regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.
Maintain positive and cooperative communication and collaboration with employees, customers, contractors, and vendors.