Johnson & Johnson ir globāls veselības aprūpes uzņēmums, kas darbojas farmācijas, medicīnas ierīču un patērētāju veselības jomā. Tā pētniecības un produktu izstrādes darbība ietver onkoloģijas, imunoloģijas, neirozinātnes, kā arī sirds un plaušu slimību zāles un terapijas, līdztekus MedTech risinājumiem sirds un asinsvadu aprūpei, ortopēdijai, ķirurģijai un redzes aprūpei. Uzņēmuma plašākā darbība ietver arī veselības un labklājības izglītību, liela mēroga ražošanu, darbu ar investoriem un globālas sociālās ietekmes iniciatīvas, radot iespējas zinātnes, klīniskā darba, inženierijas, ražošanas, komercdarbības un uzņēmuma funkcijās.
Experienced SAP Quality Management Process Analyst – Johnson & Johnson, Cork (Hybrid)
Experienced Process Analyst leading SAP S/4HANA Quality Management deployment for Johnson & Johnson’s pharmaceutical ERP transformation. Oversees global QM implementation, testing, compliance, and batch traceability.
Īrija52 400 € – 82 915 € / gads
HibrīdiPilna slodzeVidējais līmenisVecākais speciālistsNepieciešamā Valoda: angļuAnalītiķisApraksts
- Lead and support the global deployment of SAP Quality Management capabilities in coordination with NextGen QS
- Enable real-time quality event and non-conformance management across Source, Make, and Deliver operations
- Coordinate satellite-system integrations covering release management, laboratory testing, manufacturing batch-record review, and artwork key-date governance
- Establish Global Batch Traceability through a unified ERP backbone and support preparation for future GBT and BRH integrations
- Define and govern batch-determination rules to ensure compliant batch use and customer shipments
- Serve as the senior functional authority for Quality Management SMEs and analysts
- Manage workload planning, prioritization, and delivery quality
- Provide functional leadership and coaching while maintaining solution quality and regulatory compliance
- Act as the primary escalation contact for QM topics within Transcend
- Support solution confirmation with Global Template Owners, Quality Assurance, and Regulatory partners
- Oversee functional testing, validation support, and hypercare in line with GxP and CSV expectations
- Drive QM issue resolution and incorporate lessons learned into the global template
- Work with Manufacturing, Supply Chain, Commercial Execution, IT, Validation, and Quality Assurance teams
- Partner with system integrators and satellite-system owners to deliver compliant, auditable, and sustainable integrations
Prasības
- University degree or equivalent experience in Quality, Engineering, Life Sciences, or a related discipline
- At least four years of demonstrated professional experience
- Extensive knowledge of Quality Management processes in GxP-regulated manufacturing environments
- Advanced functional expertise in SAP S/4HANA QM, including batch management, inspection processes, non-conformance handling, and release workflows
- Demonstrated experience leading or supporting SAP implementations governed by Computer System Validation and regulatory inspection requirements
- Proven people-management experience with responsibility for functional delivery and quality results
- Experience integrating SAP QM with quality satellite systems such as NextGen QS, LIMS, or electronic batch-record platforms
- Experience with Global Batch Traceability or Batch Record Hub concepts or implementations
- Previous participation in global ERP transformations in the pharmaceutical or life sciences sector
- Willingness and ability to travel domestically and internationally up to 50% of the time
Priekšrocības
- Annual bonus with a target determined by pay grade and location
- Vacation days
- At least 12 weeks of parental leave
- Bereavement leave
- Caregiver leave
- Volunteer leave
- Well-being reimbursement
- Programs supporting financial, physical, and mental health
- Service-anniversary and recognition awards
- Insurance plans for employees and, where applicable, eligible dependents
- In the Netherlands, annual base pay includes an 8% holiday allowance