Process EngineerEngineering & TechnologyKapuni (NZL)Professional - Experienced32-40 hoursJob-ID : 52000Process EngineerDid you know that you already know us? Almost every second tablet which is on the global market contains our products. This demands great entrepreneurial power so that we are always looking for people who take ownership and are not afraid of accountability.Now it is your chance to join!Process EngineerWhat we ask5+ years' experience, preferably in powder processing or infant formula / pharmaceutical industryFluent in EnglishStrong communication skillsStrong focus on quality and accuracyStrong analytical skillsExperience in project management / contractor managementRelevant Bachelor Degree or equivalent preferredKnowledge of cGMP requirements preferredExperience in operational excellence is preferredWhat we offerAn international work environmentWorking in a science based and solution driven teamContinuous learning and development; your development is not only good for your career; we also benefit from itExcellent remuneration packageShort communication and short decision linesYou are seeing this because you have not accepted our advertising cookies.If you want to see our videos, please change your cookie preferences.Vacancy descriptionIdentification and implementation of production process improvements.Organisation of production trials and implementation of new products.Validation of automation, process and equipment changes.Ensuring control of analytical test methods.Problem solving, deviation and failure investigations.Management of R&D / technical projects, including investments (capital requests)DFE contact for relevant process development projects in Fonterra (TGL).Sympatec key user, responsible for monitoring SPR and reporting when outside limits.As TQF operator responsible for maintaining TQF certificate.Responsible for annual review and updates of HACCP.Responsible for annual review and update of CMDB and OT MasterplanMonthly reporting on KPIs allocated to Site Engineer responsibilitiesEnsure compliance with all regulatory, health, safety, customer and DFE standard & requirementsCompilation and Review of completed batch documentation in absence of Site ManagerWork with regulatory affairs manager to ensure timely updates of DMF and maintaining FDA registrationAssuring a high quality of work permits within the shifts through monthly Permit / SWS reviewsReview plant Work Instructions to ensure they are up to date with changes to customer, regulatory and DFE business system requirements.Ensure plant operates efficiently through all stages from receipt of raw ingredients and packaging materials to final product dispatch.Continuous improvement of equipment, processes and safety and wellbeing.The Site enginer is the allocated Deputy Environmental Management Representative (DEMR)Team DetailsReports to the Site ManagerDirect reports :Connects to DFE Pharma's Global Engineering community#J-18808-Ljbffr
