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Manufacturing Technical Trainer

Location
Lodi, California
Job Type
Permanent
Posted
15 Oct 2020
POSITION SUMMARY:Responsibilities of this role include developing, leading and coordination of training schedules, training compliance monitoring, training system improvements, and onboarding within the manufacturing team.Technician Trainer support operations on the floor and is required to engage in Quality, Compliance, Safety and Continuous Improvement Initiatives.ESSENTIAL JOB RESPONSIBILITIES:AssistSupervisors/TrainingSpecialists in coordinating, delivering, and monitoring training activities that directly affect manufacturing processes, including QSR/GMP complianceFacilitate and deliver classroom training sessionsDevelop and implement computer base trainingServe as the point of contact for specific learning programs, as assigned.Facilitate focus groups and conduct needs assessments, under the guidance of managementServe as back-up Learning Management System Administrator (eLMS).Maintains and generate all Manufacturing personnel records of training activities, on the job training records and certificationCommunicate frequently; reporting on audit findings, Associates feedback and individual performance results to management. Ensure compliance with all Standard Operating Procedures (SOP's), Standard Work (SW) and Work Instructions (WI's)Support training for all key personnel and end usersAchieve a high level of Associates satisfaction from training sessionsTeaches and models technical skills, concepts, resources and toolsAssists participants in developing specific skills related to the processProvides individual instruction and training as neededAssesses needs of participants and modifies class content or teaching methods to meet those needs.Applies evidence-based education techniques in teaching methods.Answers questions and provides training participants with appropriate resources of information.Arranges and coordinates room set-up, availability of materials and audio/visual equipment.Administers and collects class evaluation forms and assessmentsConducts follow-up and monitor progress of traineesBecome a recognized expert in technical areas and including competencies to answer a wide range of questions regarding Manufacturing processesMaintains and promotes knowledge and utilization of resources related to Manufacturing processCompletes required continuous training and education such as those related to workplace safety, legal and regulatory compliance, accreditation and licenser requirements and department specific requirementsPerform regular floor audits80% on the manufacturing floor and 20% administrative workMINIMUM REQUIREMENTS:Education or Experience (in years): High School degree (or equivalent) with 4+ years manufacturing experience with training experience and advance computer proficiency. Preferably in an ISO 9001 certified medical device company and proven knowledge of GMP/QSR/FDA/ISO regulations and compliance requirements.ORBachelor's degree in relevant field with advance computer proficiency and social skills.Knowledge and skills: Experience in compiling data to support metrics analyzing current process.Experience in using precision toolsExperience in program development and creationKnowledgeable in Advanced Microsoft Office software.Ability to interface effectively with a cross-functional team environment.Strong attention to details skills.Ability to use tools such as magnifying glass, and other handheld toolsAbility to work and communicate with people at all levels from assemblers to engineers to managementProficiency on PC, MS-Word, Powerpoint and MS-EXCELAbility to communicate effectively and facilitate group trainings.Physical requirements/abilities: Posture and Movement equal to but not less than requirement of the following:Position1-2 hours2-4 hours4-6 hours6-8 hoursStandWalkSitBendReachGraspPush/PullSquatPREFERRED REQUIREMENTS:Understand basic Manufacturing processing and the relation to defects.Must have basic inspection techniques. Intermediate knowledge and experience with SAP/MES ERP.4+ years manufacturing experience preferably in an ISO 9001 certified medical device company and proven knowledge of GMP/QSR/FDA/ISO regulations and compliance requirements.Experience in a Quality EnvironmentDanaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The "EEO is the Law" poster is available here.
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Details

  • Job Reference: 182900729-2
  • Date Posted: 15 October 2020
  • Recruiter: Cepheid
  • Location: Lodi, California
  • Salary: On Application
  • Sector: Manufacturing Operations
  • Job Type: Permanent