Biologics Sourcing Manager, IMSCP (Single Use Technology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Location: Hybrid role based in Titusville, New Jersey, United States; Cork, Ireland; or Zug, Switzerland. On-site work is required at least three days per week, with up to two remote days. Up to 15% domestic and international travel may be required.
Base pay: €70,100–€121,210 annually, plus an annual bonus or sales commissions depending on pay grade and location.
Company
Johnson & Johnson develops healthcare solutions across Innovative Medicine and MedTech, including medicines and technologies intended to improve patient outcomes.
What you will do
- Lead strategic and critical supplier relationships for Single Use Technology materials used in biotherapeutics drug substance manufacturing.
- Execute sourcing events, develop negotiation strategies, and negotiate supplier agreements to improve cost, service, flexibility, and supply assurance.
- Implement the global category strategy through supplier diversification, standardization, specification simplification, and resilience initiatives.
- Partner with Supply Chain, Planning, Quality, manufacturing sites, R&D, technical teams, Legal, Finance, and suppliers to resolve performance, quality, availability, and lead-time issues.
- Support risk assessments, business continuity planning, alternative supplier qualification, product introductions, technology transfers, capacity expansions, and manufacturing readiness.
- Maintain sourcing, contracting, savings, supplier-performance, and risk-management records while supporting procurement excellence and continuous improvement.
Requirements
- Bachelor’s degree or equivalent in Business, Supply Chain, Economics, Engineering, Science, or a related discipline.
- At least five years of relevant professional experience in Procurement, Supply Chain, Operations, Engineering, supplier management, or a related field.
- Experience with strategic sourcing, category management, supplier relationship or performance management, and contract management.
- Demonstrated ability to lead sourcing projects, negotiate commercial agreements, analyze business and financial information, and influence stakeholders without direct authority.
- Strong project-management, communication, analytical, judgment, and execution skills in complex cross-functional environments.
- Ability to work across global teams and time zones and to work on site at least three days per week.
Nice to have
- Experience in pharmaceutical, biopharmaceutical, life sciences, medical technology, or another highly regulated industry.
- Knowledge of bioprocessing, biotherapeutics drug substance operations, or Single Use Technology.
- Experience with supplier performance management, supply market analysis, cost modelling, procurement excellence, or business continuity initiatives.
- Experience supporting new product introductions, manufacturing network expansion, technology transfers, or launch-readiness programs.
- Professional certifications such as CPSM, CSCP, CPIM, or PMP, or an MBA or other relevant advanced degree.
Culture & Benefits
- Inclusive work environment guided by the company’s Credo and focused on patient impact.
- Vacation days, parental leave of at least 12 weeks, bereavement leave, caregiver leave, and volunteer leave.
- Well-being reimbursement and programs supporting financial, physical, and mental health.
- Insurance plans, subject to applicable plan terms and location eligibility.
- Service anniversary and recognition awards, with compensation and benefits varying by location.
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