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QC Supervisor Nights at Thermo Fisher Scientific
Thermo Fisher Scientific
Lebanon, NH
Manufacturing
Posted 0 days ago
Job Description
Work ScheduleThird Shift (Nights)Environmental ConditionsCleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowedJob DescriptionResponsibilitiesCoordinate daily quality control activities in accordance with design and process documentation to meet safety quality output on-time delivery targets and revenue activities are completedParticipate and lead improvement events (such as Kaizen 5S Practical Process Improvement); coach and mentor direct reports to drive continuous improvement as a way of lifePartner with the Operations team to facilitate understanding of quality expectations and requirementsLead daily quality control meetings and create and publish daily/weekly/monthly metricsLead training and coaching of direct reports and complete annual performance reviewsEnsure adherence to company policies and procedures holding staff accountable and working with human resources to apply corrective action as requiredIdentify quality constraints and resolve issues including resolving material concerns prioritizing support functions (receiving inspection mfg. engineering etc.) and escalating issuesExecution of root cause correction plan on any metrics not meeting targetEnsure that safe work practices are in use including teams adherence to Personal Protective Equipment (PPE) requirements of the job functionAssist with 3rd party auditsDirect the daily workload to ensure schedule completion while managing utilization and efficiencyBuild and develop a disciplined workforce that adheres to all procedures and Work Instruction DocumentsAbility to have flexible work schedule and cover shifts as needed. Weekday and Weekend shiftsAssist in TrackWise investigation and Root Cause investigation.How will you get hereHigh School Diploma or GED bachelors degree from an accredited University preferredMinimum 3 years experience leading teamsExperience working in a regulated environment (medical device or pharmaceutical preferred)Knowledge Skills Abilities3-years experience leading a team in a professional work environmentWorking knowledge of Microsoft Office (Word PowerPoint Excel)Problem solving skillsWritten and verbal communication skillsAbility to coordinate and work on multiple projects with other departments or functionsAbility to mentor train motivate and coachPreferred experience working in a ISO9001 ISO16949 or ISO13485 environment.Preferred experience with Continuous Improvement Lean Manufacturing and/or Six Sigma experienceRequired Experience:Manager Key Skills Bidding,Food Safety,IT Audit,Compliance,Actuarial,Airport Employment Type : Full-Time Experience: years Vacancy: 1
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