
Senior Manager - R&D Compliance and Technical Services
- Kildare
- Permanent
- Full-time
- Responsible for development, implementation, and monitoring/horizon scanning of compliance programs related to Ireland R&D processes, ensuring adherence to relevant laws, regulations, and industry standards in both US and EU geographies (e.g., FDA, ISO, GMP, GHS, ECHA etc.).
- Manage and oversee technical services that support R&D activities, including chemistry lab infrastructure, software systems, IT solutions, and R&D EHS.
- Lead R&D Technical Services strategic capability & infrastructure investment projects.
- Lead, mentor, and develop a high-performing team of compliance and technical services professionals & specialists.
- Collaborate with Global R&D Functions to ensure that new product development, testing protocols & sensory meet compliance and quality standards.
- Ensure compliance with local, national, and international environmental, health, and safety regulations applicable to R&D ingredients, semi-finished goods, operations & projects.
- Drive continuous improvement initiatives related to compliance and technical service efficiency within the Ireland R&D function.
- Provide expert guidance on regulatory, EHS and all technical requirements during project planning, execution, and review phases.
- Lead audits, risk assessments, and investigations related to R&D compliance, ensuring timely resolution of any non-conformances or deviations.
- Develop and deliver training programs to enhance compliance awareness and technical competence among R&D staff.
- Manage strong relationships with the KDP Applied Sciences Function in US, external regulatory bodies, technology vendors, and service providers.
- Manage R&D budgets, project timelines, and resource allocation effectively.
- Bachelor's degree in Scientific/Pharma disciplines, or related field; advanced degree preferred.
- Minimum 8+ years of experience in R&D compliance, analytical services and/or technical services in regulated industries (Food & Beverages, pharmaceuticals, biotech, medical devices, or similar).
- Strong knowledge of regulatory frameworks and standards applicable to R&D activities (e.g., FDA, EMA, ISO 13485, GLP, GHS, ECHA).
- Proven experience managing compliance programs and technical operations in R&D settings.
- Excellent leadership, communication, and cross-functional stakeholder management skills.
- Ability to analyze complex regulatory requirements and translate them into actionable policies and procedures.
- Strong problem-solving skills and a proactive approach to risk management.
- Experience with laboratory information management systems (LIMS), validation protocols, and technical support tools is highly desirable.
- Ability to travel domestically and internationally as required
- Knowledge of the EU Regulatory environment
- Familiarity with emerging testing and analytical technologies and digital tools in R&D
- Experience in cross-functional collaboration in multi-national matrixed organizations