How you will contribute
Accountable person for the site for analytical agenda; capability measuring of people and equipment, compliance to internally defined testing equipment, testing methods, proficiency testing, specifications and calibration of equipment. Manage the Analytical scientist and provide development opportunitiesAccountable person and site subject matter expert (SME) for compliance to internal specifications and escalation of any deviations, managing site specification control plan. Leading programme during internal and external audits.Accountable person and site SME for compliance to internal monitoring and measuring QP including Measurement Systems Analysis (MSA)/Attribute Agreement Analysis (AAA) for equipment and people for critical to quality (CTQ) measurements. Maintaining site calibration register compliance. Leading programme during internal and external audits.Accountable person and site SME for compliance to Net Contents legal, regulatory and internal controls for in-line and off-line weighing. Leading programme during internal and external audits.Accountable person and site lead for timely monthly KPI reporting of consumer complaints – including analysis trending and key drivers. cpm and capability reporting of variable CTQ’s. Parts Per Million (PPM) reporting of attribute CTQ’s. Providing updates to Corporate QualitySite sensory champion, ensuring compliance to internal requirements to maintain level 2 sensory siteDigital Quality Records Management system (IQS) – site administrator and SME for the site. Maintain and update the system, implement new sampling requirements/tests as required, provide day to day troubleshootingLean implementation – Site Lead for QM Pillar roll out, lead meetings and activities linked to QM Pillar roll out, lead phase assessments, represent QM Pillar on Leadership Pillar. System Work Process (SWP) owner for Consumer Focus and Manufacturing Standards (including Qualification in SWP)Provide day to day support on incidents for the wider Quality TeamSite Lead for (Consumer Inspired Quality) CIQ agenda – non food safety agendaLead own agenda’s during internal and external auditsLead Internal audits both desktop and plant based for the clusterCarry out monthly GMP audits within BournvilleParticipate, conduct and coach teams through internal investigations and root cause analyses, for any quality compliance incidents including, consumer & customer complaints, out of specification results, internal audits and factory/GMP issues. Create, support and/or approve the maintenance of SOP’s, work instructions & methodologies linked to any quality criteria and specifications. Prepare and maintain quality related documents for processes and products. Ensure site documentation is in line with Global Quality Policies.Coach and train operational teams in all aspects of Quality Management where directed. Engage in daily morning meetings with the core teamSupport Quality training, education and coaching with specific responsibility for maintaining, updating and training of Date and Batch Code, Net Contents and IQS for both operators and shift leadership sign off Support Quality engagement programs.Know the ethical and legal compliance responsibilities of the position; raise questions and concerns when faced with an ethical or compliance issue; apply integrity in all aspects of professional conduct.Complete other work required as directed by the Quality Manager or delegates to support continuous improvement.Key measures.
Reduce Quality loss. (Internal NC’s, Customer complaints etc.)QP Global Audit successes.Reduction in CPMU.Robust systems management and maintenance.Quality continuous improvement projects implemented.Successful external audits and other supply chain audits and visits.What you will bring
A desire to drive your future and accelerate your career and the following experience and knowledge:
Experience of Food Safety and/or Quality within a manufacturing environmentAudit experience (plus FSCC 22000 Lead Auditor desirable)Stakeholder management across all levels of the businessAnalytical mindset with ability to handle and interpret many different data setsLean/Six Sigma/TPM experience and knowledge desirableAn accountable, honest, hardworking work ethicFlexibility and adaptability to meet customer/business requirementsMeticulous attention to detail and an ability to follow verbal and written instructionsGood written and verbal communication skillsSelf-motivation, enthusiastic and quick to learnWorking well individually or as a member of a teamOrganisation skills that allow for working on multiple activities concurrentlyComputer literacy in standard MS office applications, strong Excel skills (PowerBI and Minitab preferred).More about this role
Work schedule: 100%
Relocation Support Available? Country to country Relocation support available through our Global Mobility PoliciesBusiness Unit SummaryWe value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!Our people make all the difference in our succesMondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Excited to grow your career?We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!
IF YOU REQUIRE SUPPORT TO COMPLETE YOUR APPLICATION OR DURING THE INTERVIEW PROCESS, PLEASE CONTACT THE RECRUITERJob TypeRegularSupply Chain Quality AssuranceProduct Quality, Safety and Compliance