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Global Process Owner for Product Life Cycle (PLM)

Posted 25 days ago

  • London, Greater London
  • Any
  • External
  • Expires In 2 months
Site Name: UK - London - Brentford, Belgium-Wavre, UK - County Durham - Barnard Castle, UK - Hertfordshire - WarePosted Date: May 20 2024We’re excited to be moving to our vibrant new home on New Oxford Street in central London from the end of June 2024. At GSK HQ, we’re building an energising space where we can connect, collaborate and get ahead of disease together. Designed especially for us, it’ll be one of the healthiest workplaces in the world, with best-in-class tech and bright, light spaces to help us thrive.Global Process Owner for Product Life Cycle (PLM)We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 2.3 billion packs of medicines and doses of vaccines in 2023.We continue to modernise, so we can launch even more new products at speed whilst continuing to deliver across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions, and artificial intelligence to deliver for patients.The Global Process Owner for Product Lifecycle will be accountable for new product introduction, extension & lifecycle management in Supply Chain. They will lead an initiative to understand current processes & principles around product definition, build a consistent ‘to be’ standard incorporating inputs from transformation programmes and other customer requirements. Define impact of change, develop a roadmap, and deliver.This position will be a 2-Year Fixed Term Contract.Key Responsibilities include, but are not limited to: Responsible for Digital Product Definition in Supply Chain:Accountable to ensure all digital elements that constitute a unique SKU are consistent and processes interact effectively (incl GTIN/Serialisation)Accountable for the structure of SKU to ensure product can be effectively grouped with like material (Type/Stage/Status/Hierarchy)Accountable for management of SKU change process in SC including:Definition of what constitutes a requirement for SKU change.E2E Process to execute change that ensures all required changes in various systems are understood and factored in.As owner of portfolio management process, you will develop a consistent approach and ensure you meet business requirements. Other responsibilities Include: Support design & implementation of PLM solution in Supply Chain to support visibility of history of change & enable alignment of change with regulatory status.Key understanding of core Supply Chain systems – MyPSR/MySKU, ERP/OMP/Glams/ATTP/ES) and role played in launch.Understand current & future system architecture and impact on PLM.Design input to S4 on data process & drivers of SKU change including workflow management, system integration, data provision & master data management to enable NPI.Why you? Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:Degree qualification or equivalent in a Supply Chain or related subject. Considerable experience as a leader who can demonstrate influencing skills at multiple levels of the organization.Commercial awareness of NPI & SKU launch process and the principles underlying the procedure.Global experience obtained either by working at regions or as part of a central organisation delivering / operating globally. Proven experience in planning team actively and managing product lifecycles.Preferred Skills If you have the following characteristics, it would be a plus: Regulatory knowledge and experience on how to manage market approval & product changes.Previous experience with Quality Systems & Data to align on change control processes and impact on SKU definition.Experience with R&D including PDLM solution and Digital Tech TransferLean six sigma skills at green belt or above.Closing Date for Applications: 28th May 2024 (EOB)Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only).We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on ##### or 0808 234 4391. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive .As you apply, we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it.
Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.
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