A leading health and wellness provider is seeking a mid-level Packaging Engineer for their Packaging Innovation Centre. In this role, you will develop and implement sustainable packaging solutions while ensuring compliance with regulations. Candidates should have a degree in relevant engineering fields and at least 2 years of packaging development experience. Strong CAD skills and understanding of packaging materials are essential. #J-18808-Ljbffr
A leading healthcare company in Dublin seeks an experienced Regulatory Affairs Manager to lead regulatory strategy for biocidal products. Responsibilities include lifecycle management, regulatory submissions, and team leadership. The ideal candidate will have at least 5 years of experience in Regulatory Affairs and a strong understanding of EU regulatory frameworks. This position offers a hybrid working model and competitive benefits. #J-18808-Ljbffr
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®, 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. Description Overview Perrigo is seeking a dynamic and experienced Regulatory Affairs Manager to lead regulatory strategy and execution for our biocidal product portfolio across multiple territories. This role offers a unique opportunity to shape regulatory pathways, drive compliance excellence, and lead a high‑performing team within a fast‑paced, innovation‑driven environment. Scope of the Role Strategic Regulatory Leadership Lead the regulatory lifecycle management of biocidal products, including licensing, renewals, variations, and post‑marketing activities. Develop and implement regulatory strategies aligned with business objectives and evolving regulatory frameworks (e.g., BPR, REACH, CLP). Serve as the subject matter expert on biocides, providing strategic guidance to internal stakeholders and senior leadership. Team Management & Development Manage and mentor the Biocides Regulatory Affairs team, fostering a culture of accountability, collaboration, and continuous improvement. Set clear objectives, monitor performance, and support professional development within the team. Cross‑Functional Collaboration Partner closely with cross‑functional teams including R&D, Quality, Supply Chain, Commercial, and Legal to ensure regulatory alignment and support product development and market access. Actively contribute to regulatory input in innovation projects, product launches, and strategic business initiatives. Technical Excellence Prepare, review, and submit high‑quality regulatory dossiers for active substances and product authorisations under the Biocidal Products Regulation (EU BPR). Maintain up‑to‑date knowledge of EU and international regulatory requirements for biocidal products, including emerging trends and legislative changes. Ensure regulatory compliance across all relevant markets and proactively manage regulatory risks. Experience Required University degree in Chemistry, Biology, Pharmacy, or related scientific discipline; advanced degree preferred. Minimum 5 years experience in Regulatory Affairs, with a strong focus on biocidal products and chemical regulations. Proven experience in preparing and submitting dossiers under BPR, REACH, and CLP. Demonstrated leadership experience, including team management and stakeholder engagement. Strong understanding of regulatory frameworks across EU and global markets. Excellent project management skills with the ability to manage multiple priorities and deadlines. Fluent in English; additional European languages are a plus. Strategic thinker with a hands‑on approach and a passion for regulatory excellence. Strong interpersonal and influencing skills, with the ability to build trust and drive alignment across diverse teams. Detail‑oriented, analytical, and solution‑focused. Resilient and adaptable in a dynamic regulatory and business environment. Committed to continuous learning and professional growth. Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to support you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more about Total Rewards at Perrigo. Hybrid Working Approach We love our offices and the setting they provide for in‑person collaboration and celebration. We also appreciate the opportunity to work remotely to energise you, so we promote flexibility with the ability to work two days a week from home in many roles. We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here . Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. 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. #weareperrigo #J-18808-Ljbffr
Senior Legal Counsel, Enterprise Contract Management and Risk Join to apply for the Senior Legal Counsel, Enterprise Contract Management and Risk role at Perrigo Company plc 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®, 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. Description Overview In this position, you will report directly to the Vice President, Assistant General Counsel and will provide comprehensive legal support with a focus on overseeing the end-to-end management of all contract processes, drafting, and negotiation within the enterprise, encompassing both procurement and sales agreements. You will be responsible for creating, managing, and deploying contract playbooks, clause libraries, and trainings across the organization and supporting the Legal & Governance function in its contracting needs. You will also oversee the lawyers in the contract team, ensuring best processes and practices. The candidate selected to fill this role will be based at our Dublin or Warsaw offices. Scope of the Role Oversee the end-to-end management of all contract drafting and negotiation within the enterprise, including both procurement and sales contracts. Create, manage, and deploy contract playbooks, clause libraries, and training programs across the organization to ensure consistency and efficiency in contract management. Continually analyze and assess enterprise integrated contract and operational risks. Provide legal support, counsel, and risk assessment on complex contract-related matters, ensuring all contracts comply with relevant laws and regulations. Monitor changes in global contract law and compliance regulations, and work with business units to address these developments. Collaborate with the compliance team to evaluate the company's activities, policies, practices, and transactions to safeguard the company's legal and business interests. Provide legal support for critical business development, mergers and acquisitions, and other initiatives, particularly in the areas of contract due diligence and advice. Assist the litigation department in managing, monitoring, and advising on any contract-related disputes or claims made, including the management of external counsel as needed. Collaborate with the contracts teams to prepare/review proposed contracts and other legal documents to protect the company's interests. Collaborate with Legal Operations to implement and manage contracting technology. Experience Required A qualified and licensed attorney. You will typically have 10+ years of experience in contract management and negotiation. The key experience sought is expertise in creating, managing, and implementing contract playbooks, clause libraries, and training programs. Strong ability to analyze and ingrain technology solutions into processes - strong technology acumen. People Management - Experience managing lawyers in a global organization. Broad experience as a legal advisor to a global business in an in-house corporate legal department. Strong analytical skills, attention to detail, and the ability to work collaboratively in a fast-paced environment. Experience advising on contract matters in regulated industries, preferably in selfcare or consumer goods. Excellent communication and leadership skills. Benefits We 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. Find out more about Total Rewards at Perrigo. Hybrid Working Approach We 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. Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. 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. #weareperrigo Seniority level Mid-Senior level Employment type Full-time Job function Legal, Management, and Strategy/Planning Industries Pharmaceutical Manufacturing, Research Services, and Manufacturing #J-18808-Ljbffr
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®, 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 win in self‑care. Description Overview The Packaging Engineer role is a mid‑level position within Perrigo’s Packaging Innovation Centre of Excellence (COE). This position is responsible for the development, improvement, and implementation of packaging solutions that deliver value, performance, and sustainability. Operating with a level of technical autonomy, the Packaging Engineer leads packaging development initiatives ensuring that Design‑to‑Value (DtV), recyclability, and sustainability are central to every solution. Reports To: Packaging Innovations Manager Scope of the Role Serve as the packaging development lead on one or more medium‑to‑large projects, providing end‑to‑end technical leadership from concept design through validation and launch. Translate business objectives and consumer insights into innovative, compliant, and cost‑effective packaging concepts. Lead manufacturing troubleshooting and provide on‑site support for line trials, validations, and root cause investigations. Manage packaging documentation, specifications, and qualification reports in accordance with regulatory and quality system requirements. Partner cross‑functionally with Marketing, R&D, Operations, Quality, and Procurement to deliver consumer‑preferred, cost‑effective, and scalable packaging solutions. Build and maintain strong external partnerships with suppliers, CMOs, and technical experts to advance packaging innovation and resolve technical challenges. Communicate project risks, progress, and recommendations effectively to internal stakeholders. Embed Design‑to‑Value (DtV) methodologies into packaging development to balance cost, quality, and consumer experience. Evaluate and improve packaging recyclability in alignment with EU PPWR and EPR requirements. Drive material and process optimization to reduce environmental impact, minimize waste, and enhance operational efficiency. Support Perrigo’s Open Innovation and Sustainability strategies, introducing recyclable, mono‑material, and low‑carbon packaging solutions. Provide day‑to‑day technical support to ensure project quality, consistency, and compliance across active packaging programs. Contribute to the creation of best‑practice documentation, technical specification standards, and continuous improvement initiatives within the COE. Experience Required Degree level qualification in Packaging, Mechanical, Manufacturing, or Industrial Engineering, or related discipline. Typically the experience required for this role would come from 2+ years of relevant experience in a packaging development or FMCG environment, with exposure to a broad range of components (e.g., blisters, bottles, spray pumps, folding cartons, etc.) Strong understanding of packaging materials, processes, and tooling, including thermoforming, sealing, labeling, and filling. Skilled in AutoCAD, SolidWorks, ArtiosCAD, TOPS, or equivalent CAD software. Demonstrated ability to create and manage packaging specifications, 3D mock‑ups, and pallet configurations. Experienced in distribution testing (ASTM/ISTA), IQ/OQ/PQ validation, and root cause analysis. Familiarity with ISO, FMEA and DOE. Knowledge of ERP systems (SAP preferred) and project management software desirable. Benefits We 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. Find out more about Total Rewards at Perrigo. Hybrid Working Approach We 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. We are proud to be included in the Forbes list of “America’s Best Employers by State 2024”. Find out more here . Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. 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. #weareperrigo #J-18808-Ljbffr
Associate Director - CMC Regulatory Affairs Join to apply for the Associate Director - CMC Regulatory Affairs role at Perrigo Company plc 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®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves in fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Description Overview As Associate Director, you will lead the development and execution of cutting‑edge Chemistry, Manufacturing & Control (CMC) strategies, ensuring the highest standards of regulatory excellence across our diverse portfolio—from pharmaceuticals and medical devices to supplements, cosmetics, and beyond. You will contribute to the creation of robust quality dossiers and the seamless navigation and influencing of regulatory landscapes, turning challenges into opportunities for innovation and growth. By delivering timely submissions and proactively identifying risks and mitigation plans, you’ll enable first‑to‑market approvals that enhance Perrigo’s reputation as a global leader in CMC. You will inspire and empower a high‑performing regulatory team, instilling a culture of agility, compliance, and continuous improvement. Scope of the Role Lead global CMC regulatory strategy and execution for innovation projects, post‑approval changes, lifecycle management, and compliance across all product categories. Oversee the preparation, review, and submission of high‑quality CMC documentation (e.g., Module 3, Quality Overall Summary) for global health authority submissions, including new MAAs/NDAs/ANDAs, variations, renewals, and compliance updates. Develop and implement response strategies for regulatory queries and deficiency letters related to CMC matters. Engage in technical discussions with Competent Authorities in partnership with Country Regulatory teams. Collaborate with cross‑functional teams to ensure regulatory CMC alignment with commercial strategy, manufacturing changes, and global supply continuity. Manage CMC strategy and documentation for complex CMC projects, such as tech transfers, major reformulations, and geo‑expansion. Manage CMC risks associated with ingredient challenges and develop action plans to support defence, in partnership with Regulatory Product Stewardship team. Monitor global CMC regulatory trends and new regulations and guidance. Provide product impact assessments and strategic guidance to ensure continued compliance and readiness for evolving requirements, in partnership with Regulatory Product Stewardship team. Represent Perrigo in external regulatory forums and trade associations to advocate for CMC‑related policy positions and regulatory best practices. Build and lead a high‑performing, globally distributed team with deep expertise in CMC. Foster a culture of excellence, agility, innovation, and continuous learning. Develop talent pipelines and succession plans to ensure long‑term organizational capability. Experience Required Advanced degree in Life Sciences (PhD, PharmD, MSc preferred). 15+ years of progressive experience including management roles in CMC. Proven track record of successful global submissions and approvals across diverse product categories. Strong strategic, financial, and operational acumen. Exceptional leadership, collaboration, and stakeholder engagement skills. Experience with global regulatory systems and digital platforms. Benefits We 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. Find out more about Total Rewards at Perrigo. Hybrid Working Approach We 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. We are proud to be included in the Forbes list of "America’s Best Employers by State 2024". Find out more here. 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. #J-18808-Ljbffr
Overview Senior Director, Regulatory Affairs - CMC, Regulatory Operations & Lifecycle Management Join to apply for the Senior Director, Regulatory Affairs - CMC, Regulatory Operations & Lifecycle Management role at Perrigo Company plc. 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 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 win in self-care. Description Overview As Senior Director, you will serve as the visionary leader shaping Perrigo’s global regulatory future. You will champion the development and execution of cutting-edge Chemistry, Manufacturing & Control (CMC) strategies, ensuring the highest standards of regulatory excellence across our diverse portfolio—from pharmaceuticals and medical devices to supplements, cosmetics, and beyond. Your influence will drive the creation of robust quality dossiers and the seamless navigation of regulatory landscapes, turning challenges into opportunities for innovation and growth. By orchestrating timely submissions and proactively identifying risks and mitigation plans, you\'ll secure first-to-market approvals that enhance Perrigo’s reputation as a global leader in regulatory affairs. You will inspire and empower a high-performing regulatory team, instilling a culture of agility, compliance, and continuous improvement. With your strategic insight, you will oversee lifecycle maintenance, safeguarding the ongoing compliance and success of all Perrigo products. Your leadership in regulatory operations will build a resilient framework—one that streamlines processes and advances organizational excellence. As a pivotal member of the Regulatory Affairs leadership team, your stewardship will extend beyond the company, shaping regulatory policy and advocating best practices on the world stage. Through your foresight and collaboration, you will optimize Perrigo’s portfolio, position the organization for enduring success, and uphold our mission to advance consumer health worldwide. Your legacy will be one of transformative impact, setting new standards for regulatory leadership and inspiring those around you to achieve greatness. Scope of the Role CMC Regulatory Strategy Lead global CMC regulatory strategy and execution for innovation, post-approval changes, lifecycle management, and compliance across all product categories. Oversee preparation and submission of high-quality CMC documentation (e.g., Module 3, QOS) for global health authority filings, including MAAs/NDAs/ANDAs, variations, renewals, and compliance updates. Develop response strategies for CMC-related regulatory queries and deficiency letters. Manage complex CMC projects (e.g., tech transfers, major reformulations, geo-expansion). Monitor global CMC regulatory trends; assess product impact and guide compliance strategies in partnership with Regulatory Product Stewardship. Represent Perrigo in external forums and trade associations to advocate CMC policy and best practices. Address CMC risks from ingredient challenges and lead mitigation planning with Regulatory Product Stewardship. Lifecycle Management (LCM) Leadership Establish and lead the global LCM model, structure, and ways of working. Develop and execute regulatory LCM strategies across all product categories (Drug, Device, Cosmetic, Food, Supplement, Monograph, Herbal, Biocide). Ensure seamless handover of regulatory activities post-launch with the Regulatory Category team. Lead change management for marketed products, including impact assessments, submissions, and implementation tracking. Align LCM strategies with commercial, R&D, and BD goals for growth, expansion, and cost optimization. Oversee regulatory execution of post-approval changes (variations, renewals, extensions, label updates). Collaborate with Quality, Supply Chain, and R&D to ensure robust change control and regulatory compliance. Monitor evolving global regulations and proactively update dossiers and documentation. Drive process improvements to accelerate change implementation and enhance regulatory efficiency. Provide regulatory leadership for product discontinuations, divestitures, and portfolio optimization. Ensure alignment across functions for commercial strategy, manufacturing changes, and supply continuity. Maintain oversight of regulatory tracking systems and metrics for visibility and accountability. Represent Perrigo in external LCM forums and industry groups to shape best practices and modernization. Regulatory Operations Lead global regulatory operations: submissions, publishing, document management, and systems. Develop integrated data management strategy and oversee regulatory technology platforms. Ensure data integrity, compliance, and drive digital transformation to enhance efficiency. Advance Perrigo’s regulatory digital platforms, data governance, and automation. Ensure global compliance with submission standards and evolving requirements. Organizational Leadership Build and lead a high-performing global team with expertise in CMC, Regulatory Operations, and LCM. Foster a culture of excellence, agility, innovation, and continuous learning. Develop talent pipelines and succession plans for long-term capability. Experience Required Advanced degree in Life Sciences (PhD, PharmD, MSc preferred). 15+ years of progressive experience in regulatory affairs, with leadership roles in CMC, Regulatory Operations, and Lifecycle Management. Proven track record of successful global submissions and approvals across diverse product categories. Strong strategic, financial, and operational acumen. Exceptional leadership, collaboration, and stakeholder engagement skills. Experience with global regulatory systems and digital platforms. Key Competencies Strategic Foresight & Policy Influence Scientific & Regulatory Acumen Executive Communication & Stakeholder Management Innovation Enablement & Digital Fluency Global Leadership & Talent Development Operational Excellence & Change Management Benefits We 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. Find out more about Total Rewards at Perrigo. Hybrid Working Approach We 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. We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here. Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. 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. #weareperrigo #J-18808-Ljbffr
Description Overview As the Global Head of Perrigo Regulatory Affairs, you will serve as the most senior regulatory leader within Perrigo, reporting directly to the Chief Science Officer. You will lead the global regulatory strategy and operations across all brands, geographies, and product classifications. This role is critical in ensuring regulatory compliance, driving innovation, and managing the lifecycle of Perrigo's diverse product portfolio. You will oversee regulatory submissions, health authority interactions, and compliance with global regulatory standards. You will lead a global team and serve as a key member of the Science Leadership Team, shaping Perrigo’s future through regulatory excellence and strategic foresight. Scope of the Role Global Regulatory Leadership: Define and lead Perrigo’s global regulatory vision and strategy across all categories and geographies. Serve as the senior regulatory authority, advising executive leadership and representing the company in global forums and with regulatory bodies. Align regulatory strategy with Perrigo’s innovation, commercial, and public health objectives. Regional & Category Regulatory Strategy Oversee regulatory operations across key regions: USA and International. Provide strategic regulatory oversight for all categories, including Women’s Health, Nutrition, OTC, Oral Care, and Supplements. Ensure regional strategies are harmonized with global objectives and tailored to local regulatory landscapes. Regulatory Operations & Lifecycle Management Lead regulatory input across the product lifecycle—from concept through development, approval, and post-market activities. Oversee regulatory submissions, approvals, and maintenance for all product classifications (e.g., drug, device, supplement, cosmetic). Drive excellence in regulatory operations, systems, and documentation. Governance, Compliance & Risk Management Ensure compliance with global regulatory requirements and internal governance standards. Lead regulatory crisis management and recall oversight, ensuring timely and effective resolution. Integrate regulatory intelligence and risk assessment into strategic planning following the strategic lead of Policy and Stewardship. External Engagement & Policy Influence Represent Perrigo in interactions with global health authorities, industry associations, and regulatory policy forums. Shape the external regulatory environment in alignment with Perrigo’s business and public health goals. Monitor and respond to emerging regulatory trends and challenges. Innovation Enablement & Strategic Partnerships Partner with cross functional teams to enable science-led innovation through regulatory pathways. Provide regulatory due diligence and strategic input into M&A, licensing, and business development opportunities. Support Rx-to-OTC switches and novel regulatory classifications. Global Team Leadership & Capability Building Lead, inspire, and develop a high-performing global regulatory team. Build future-ready capabilities in regulatory strategy, digital tools, and global compliance. Foster a culture of regulatory excellence, collaboration, and continuous improvement. Experience Required Degree in regulatory affairs, life sciences, or related field. 15+ years of progressive leadership in global regulatory affairs within consumer health, pharmaceuticals, or adjacent sectors. Proven track record in regulatory strategy, submissions, and health authority interactions. Deep understanding of global regulatory frameworks, compliance standards, and product lifecycle management. Strong business acumen and ability to influence at the executive level. Experience leading global teams and working in matrixed environments. Exceptional communication, negotiation, and stakeholder engagement skills. Key Competencies Strategic Vision Regulatory Expertise Leadership & Influence Innovation Mindset Stakeholder Management Operational Excellence Change Leadership Communication Benefits We 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. Find out more about Total Rewards at Perrigo. Target base salary for NJ based hire is $400k+. Working Approach Hybrid Working Approach: We promote flexibility with the ability to work two days a week from home in many roles. Equal Opportunity 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. #J-18808-Ljbffr
