Iflow Lead

Conteúdo do emprego

Why Patients Need YouAt Pfizer, our mission is to deliver first-in-class science to our customers by unleashing the power or our people. We strive to be an engaged, high-performing, and diverse organization as well as a premier launch engine leveraging innovative technology. Pfizer Global Supply aspires to be the best supply organization, a Digital leader, and be an industry leader in Quality, compliance, safety, and sustainability while delivering innovative and life-sustaining products to meet our customer needs.What You Will AchieveThrough the implementation of a Lean Production System you will install the “One Best Way” of working throughout Pfizer Global Supply (PGS), focusing both vertically (on departments) and horizontally (Door-2-Door across departments). Vertical focus is better known as IMEx – Integrated Manufacturing Excellence, while horizontal focus is iFlow – Intelligent Flow. Deployment of both perspectives will be resulting in enhanced supply reliability, increased capacity, and agility to meet customer demands while improving quality performance and competitive costs. This role will primarily focus on iFlow and your knowledge and skills will be utilized in an innovative environment to ensure reliable customer supply and achieve PGS business objectives.

• This role is responsible for leading iFlow deployments at Site, including workstream Material Supply Excellence (MSE) and Design for Flow (D4F), helping to build capabilities across teams on iFlow (MSE and D4F), initiating related Continuous Improvements (CI) Initiatives at respective T3-T1 for effectiveness and efficiency towards designed / agreed performance, and monitoring and measuring success of entire initiatives.
• This role will develop site colleague capabilities with Global support, helping them understand the IMEx approach, iFlow (MSE & D4F), the necessary lean tools and provide coaching and guidance support.
• This role will provide input into the refinement of iFlow via the Above Site IMEx/iFlow Deployment Lead.

How You Will Achieve It

• Lead successful Intelligent Flow (Iflow) at site in alignment with the Site IMEx and CI lead
• Network with stakeholders for both SME and D4F, define and align with Voice of Customer/Voice of Business, provide overall progresses.
• Coach Leaders and key internal Customers on how to manage the cultural changes requested.
• Lead successful Material Supply Excellence (MSE) progress as per agreed plan following the MSE playbook or alternative
• Identify process improvement opportunities to enhance Material Supply Excellence based on baseline Material Supply Excellence assessment
• Initiate related CI Initiatives at respective T3-T1 for designed / agreed process improvements to enable improved performance (calmness)
• Monitoring and measuring success of CI loops (e.g. Gemba)
• Ensure sustainment of IMEx Material Supply Ecosystem in alignment with the Site IMEx and CI lead according to IMEx operating standards
• Lead successful Design For Flow (D4F) progress as per agreed Site plan (product/product families) following the D4F playbook or alternative
• Identify current state for related products in scope
• Define desired / agreed future state respectively overall and detail performance goal and service level agreements between departments
• Identify necessary improvements to reach desired future state
• Ensure that process improvements are translated into role cards or service level agreements or equivalent standardization
• Ensure link to Material Supply Ecosystem with respect to parameters for new / improved standards
• Initiate related CI Initiatives at respective T3-T1 for designed / agreed improvements to enable improved performance (e.g. higher throughput and/or shorter lead time/Manufacturing Cycle time)
• Ensure adequate local (T1-T3) and Global visibility though IMEx / IMEx digital and related process (eg. Flow meeting unsing Batch tracker and Material Flow tool)
• Monitoring and measuring success of CI loops as part of IMEx (e.g. VMC, CI loop meeting, action / escalation, Gemba/coaching)
• Ensure sustainment of performance
• Partner with
• All internal stakeholders (team organization)
• Above Site Support with respect to alignment on deployment (coaching, guidance and support)
• External stakeholders (e.g. Manufactuitng Excelence leads, OPS VP) related to progress reporting
• Provide change management guidance and coaching where needed (or seek support)
• Support Maturity Healthcheck related to opportunities identified
• Partner with Site OpEx / Above Site to ensure that necessary capabilities are built as appropriate (specifically Material Supply & SAP or nGPS knowledge & skills, Lean and Six Sigma tools).

QualificationsMust-have

• Applicant must have Bachelor or BS degree in a Technical or Business field with 10 years of relevant experience, Master degree in business administration or technical discipline a plus at least five years of experience; OR a Master’s degree with more than three years of experience;
• Proven experience influencing; collaboration across various levels of the Site organization and facilitating alignment on goals, targets, etc. at site and stakeholder management capabilities for Above Site. Excellent communication skills to enable interactions in the organization
• Proven capabilities in program management; experience in successfully executing larger project; experience in integrating / motivating teams.; ability prepare/organize and facilitate workshops
• Knowledge and/or experience in IMEx or similar production systems. (Examples include production system installations, helping build lean capabilities across site teams, troubleshooting challenges, and monitoring and measuring success of deployments).
• Experienced in Lean concepts (Flow, VSM), ideal Lean Black Belt certified. This included experience in process excellence and performance improvement tools, techniques, and concepts; lean operating model inclusive of 5S, Kaizen, waste reduction, SMED, Standard Work, VSM etc.)
• Relevant operational experience in pharmaceutical industry required.
• Real world experience in process excellence and performance improvement tools, techniques, and concepts incl. Six Sigma, Lean are preferred
• Experience in SAP / ERP system use are preferred
• Experience working in pharmaceutical manufacturing or an understanding of pharmaceutical industry
• Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop, and coach others, oversee, and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

De Pfizer site in Puurs is één van de grootste productie- en verpakkingssites van Pfizer wereldwijd, gespecialiseerd in aseptische productie en verpakking. Jaarlijks worden in Puurs meer dan 400 miljoen doses injecteerbare vaccins en medicijnen geproduceerd. Deze zijn ter plaatse verpakt in ampullen, flacons, plastic flessen, spuiten en patronen voor pennen.De medicijnen die in Puurs worden gemaakt, zijn bestemd voor patiënten in meer dan 170 landen wereldwijd. 30% van de productie uit Puurs is bestemd voor ontwikkelingslanden, in samenwerking met UNICEF, WHO, GAVI en ngo’s.Met het gebruik van twee windturbines, zonnepanelen en een warmtekrachtcentrale richten we ons op hernieuwbare energie.Continuous Imprv and Proj Mgmt