Global Sourcing Manager - Direct Materials (Active Pharmaceutical Ingredients) - Mat leave CoverLocation: Dublin, IE, D02 TY74
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, ACO, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to a blended-branded business to win in self-care.
Description OverviewThis role will specifically manage API (Active Pharmaceutical Ingredients) Raw Material Categories. You will be managing a large portfolio with high annual spend for a Global Leading Self-Care company. This will be a 12 Month Contract based in Perrigo's Dublin Office with some work from home flexibility (up to 2 days per week).
Scope of the RoleService – Ensure a robust raw material supply chain is in place with identified risk mitigation factors.Cost Savings – Review and manage category spend and identify opportunities for cost savings without negatively impacting quality or service.Develop, lead and implement category strategies for each core material group.Represent Procurement in multifunctional initiatives (including alternate source approval, new product developments and new product launches).Contract/Price negotiation and management.Spend Analysis and Budget management.Internal stakeholder management (R&D, Supply Chain, Planning, Innovation, Marketing, Sales and Product Pricing team).Volume allocation management - frequent review of volume forecasts to ensure awarded/contracted vendor quantities met.Experience RequiredPrior experience managing a category with complex technical requirements.Knowledge of regulatory processes in US and Europe, especially those involving APIs (ANDAs, Monographs, filings, submissions, Variations).Knowledge of FDA & European health authorities' databases - FDA (DMF, AFR, Orange book, inspections) and EMA (CEP, active product licences), plus generating reports and detailed analysis thereof.Negotiation & Influencing – Externally for commercial discussions and internally for critical procurement issues.Very proficient in advanced MS Excel, PowerPoint & presentation skills.Ability to work under pressure.BenefitsWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Hybrid Working ApproachWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.
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We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.
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