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Posted: Wednesday, March 8, 2017 9:12 AM

Job Description:/h3:
Supervisors/Training Specialists in coordinating, delivering, monitoring and improving training activities and systems that directly affect manufacturing processes, including QSR/GMP compliance
Perform skills training and classroom training in assembly and production areas.
Participates in the implementation of new training programs and standard operating procedures.
Maintains all department training records to include on the job training records of all departmental employees and other department record keeping assigned by the training supervisor.
Demonstrates and serves as role model and a resource to trainers; responsible for coaching/mentoring trainers.
Assist in new employee orientation in manufacturing.
Train assemblers in
GMP/QSR/ISO/MDD/FDA/Hazcom regulation related SOPs.
Function as training database SEM for systems such as LMS.
Generate and maintain all training
records/certificates of manufacturing personnel (hard records and electronic database), and update (subsequent to revisions) WI/MPI/SOP files related to manufacturing production in a timely manner.
Manage Retraining program: Initiate re:training request, re:train if necessary and update training records (hard records and electronic database) subsequent to re:training, according to the re:training plan. Actively involved in corrective action follow:ups when applicable. (NCMR, Audits, etc.)
Implement and maintain Visual Training Management Tools (VTMT) on the production lines.
Works as a team member of the training team and identifies the need or suggested areas of improvement for production training.
Coordinates and collaborates with engineering, production supervisors and managers, HR and Document Control to ensure compliance for all training documentation.
Ability to perform trainer certifications and training file reviews.
Demonstrate working knowledge of the Training policy and ensure adherence to.
Empower Trainers to continuously improve the training policy, training steps, and forms.
* High School Diploma. * Preferred AA or Equivalent Experience * 2+ years manufacturing experience preferably in an ISO 9001 certified medical device company and proven knowledge of GMP/QSR/FDA/ISO regulations and compliance requirements. * Previous training experience preferred. * Proven skills in multiple manufacturing processes, demonstrated problem solving and people skills, ability to work and communicate with people at all levels from assemblers to engineers to management. * Ability to interpret specs and tolerances, knowledge of equipment such as microscope, ruler, calipers and micro:meter; and processes. * Proficiency on PC, MS:Word, MS:EXCEL, MS:PowerPoint and proficient typing skills. * Proficient with digital/video camera and related software preferred. * Ability to work overtime as required. * Ability to communicate effectively and facilitate group trainings. * Demonstrated ability to support training needs at multiple site locations. * Demonstrated high functioning ability to develop and lead training sessions for large groups of people in a classroom/public speaking format. * Ability to travel to multiple sites locally as needed.
Company Description:/h3:
Global Medical Device Manufacturing Company


• Location: Salt Lake City, west valley city

• Post ID: 11326643 saltlakecity is an interactive computer service that enables access by multiple users and should not be treated as the publisher or speaker of any information provided by another information content provider. © 2017