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Summary

a self-motivated and accomplished production shift manager with 16 years + experience of working in a Pharmaceutical company, extremely proficient in all areas relating to the running of a class 100 lean sterile/ clean facility.

Experiences

Current Experience

  • Production Shift Supervisor ( class 100 sterile manufacture )


    Since June 1998
    monitor and control production of class 100 sterile manufacture through continuous support within the sterile and clean Manufacturing areas. completed a 6 month assignment at the india bangalore site as part of global over site team. key responsibilities were to up skill the work force in readiness for moving into a new state of art production facility working to lean principles and techniques. Monitor and control production of class 100 sterile manufacture through continuous support within the sterile and clean manufacturing areas. Completed a 6 month assignment at the India Bangalore site as part of Global Over Site team. Key responsibilities were to up skill the work force in readiness for moving into a new state of art production facility working to lean principles and techniques.

Past Experience

  • Finisher

    October 1988 --- June 1998
    worked as Process Operator in the production of forming fabrics as used in the paper making industry. completed an internal auditors course with the stockport chamber of Commerce ( accredited )this was used in conjunction with the company attempting to become bs5750 iso9002 accredited.

  • Distribution router

    November 1978 --- October 1988
    during this employment i gained knowledge of high rise warehousing and became licensed to operate several type of fork lift truck, heister fork lift , reach truck , narrow isle high rise truck. i moved from the main warehouse into the distribution department where i would load and set the route Documentation for all deliveries throughout england,scotland,wales and northern ireland.

Personality

Self Assessment :
ApproachabilityAssertivenessCollaborationCommunicativeCritical thinkingDependabilityEfficiencyFlexibilityInterest in knowledgeProactivityResponsibilityResult OrientedSelf-confidenceSelf-disciplineInnovative thinkingKindnessProblem solvingService orientedTrustStrategic thinkingSociability

Knowledge

LinkedIn Assessment :
GMPManufacturingPharmaceutical IndustrySterilizationFDAValidationAseptic ProcessingSOPLean ManufacturingCleaning ValidationQuality SystemChange ControlContinuous ImprovementQuality ControlCross-functional team leadershipCAPAComputer System ValidationRegulatory RequirementsPharmaceuticsQuality AssuranceRoot Cause Analysis21 CFR Part 11GLPGXPFDA GMPQuality ManagementChange ManagementMedical DevicesTechnology transferSix SigmaProcess SimulationTrainingProcess improvementQuality AuditingLIMSBiopharmaceuticalsAnalytical Chemistrydevelops people and organisationRegulatory affairsLeadershipV&VBiotechnologyOperational Excellence

Skills and Expertise

Self Assessment :
Aseptic processingAseptic techniquesAssess adverse reactionsAssess product quality issuesAssess quality process issuesAssist with proceduresAssist with routine testsAssist with experimentsAssist with site trainingCoachCoach staffChemistry Manufacturing and Controls (CMC) activitiesCollaborate with project teamCollect dataCommunicate effectively on different company levelsCommunicationCoordinationData entryDetermine availability of facilities and equipment at the siteDetermine needsDirect co-workersDirect co-workers to achieve resultGuide staffGuide studentsHandle callsHandle incidentsIdentify growth / improvement potentialIdentify risksImplement Key Performance Indicators (KPI's)Implement ProcessesLead teamsLiaise with professionals in other divisions of the company as requiredlifescienceMaintain strong relationshipsManage aseptic riskManage risksManufacture of GMP batchesManufacture of non-GMP batchesManufacture of non-GMP and GMP batchesMonitor Key Performance Indicators (KPI's)Provide support for scientific and/or technical projectsProvide trainingReport Key Performance Indicators (KPI's)Report serious adverse events (SAE)

Education

  • in from Bradbury County Secondary school for Boys in 1977

Training and Certification

  • City and Guild qualification in class 100 sterile manufacture in 0000 Certification
  • City and Guild qualified in sterile / clean area design in 0000 Certification

Languages

BrightOwl Assessment:
Self Assessment:
English
Native

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Production Manager Production Supervisor
  • Locations I am interested in:
  • Work From Home:
    No
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Macclesfield, United Kingdom

Others

Driving License
  • Yes

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