Head of Regional R&d Quality
vor 2 Monaten
Description
**Head of Regional R&D Quality**
The Head of R&D Quality & Compliance (Q&C) in EMEA, is a member of the EMEA Q&C Leadership Team. The Head directs employees at the sites performing R&D Q&C activities within the region to ensure an integrated, comprehensive risk-based quality monitoring system for GMP, Analytical and Micro activities is developed, implemented and maintained. Quality monitoring activities include but are not limited to:
Functions as an advisor concerning Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) and provides appropriate compliance guidance to employees and R&D personnel. Contributes to implementation of processes and systems that lead to collection of data relevant to reporting, evaluating and actions on quality metrics.
Participates in Regional R&D and Quality & Compliance leadership teams. Using available information and relevant metrics, collaborates with other members within the EMEA Quality & Compliance leadership teams and R&D in identifying areas of continuous improvement to the global quality management framework of R&D within the Kenvue.
Acts as the single point of contact for region and ensures appropriate escalation processes are implemented. Leads efforts for establishing R&D Quality & Compliance processes and guidelines and participates in process improvement projects, departmental decision-making, recruitment, resource assessments, budget management and end of year performance evaluations. Performs interdepartmental and cross-functional strategic planning. Conducts L&A activities, as required, liaising with the applicable R&D and Quality & Compliance personnel.
Responsible for the development of all employees within the department by supporting the development of Human Resources Planning (HRP) programs including management development and training to meet current and future business needs. Provide an environment which encourages the company's credo, commitment to equal employment opportunity and the value of a diverse work force.
**Major Duties & Responsibilities**
Provide strategic management oversight and leadership to the EMEAl R&D Quality & Compliance organization, implementing quality monitoring programs to proactively ensure the R&D organization is operating in compliance with company/division policies and procedures, as well as applicable regulatory requirements. Ensure innovative compliance solutions are identified, when possible, to address project and process challenges. Ensure effective deployment of R&D Quality & Compliance resources to meet the current and future needs of the R&D organization.
Provides ongoing mentoring, coaching and development of R&D Quality & Compliance employees. Ensures employees are trained in procedures and systems associated with their assigned tasks. Perform administrative tasks associated with performance reviews, salary administration, and other personnel tasks. Responsible for the regional budget planning process and management of regional budgets. Recruits/hires qualified employees for the department and ensures employees have the education, experience and tools to appropriately function as advisors of GMP, Good Documentation Practices and other applicable requirements.
Participate in the Regional R&D and the Regional Quality & Compliance Leadership Teams, providing R&D Quality & Compliance support to strategic discussions/decision making. Lead R&D Management Reviews and other compliance activities in the regions and escalate issues appropriately. Collaborate withing and across regions and with Global Regulatory Compliance & Standards to evaluate compliance trends and ensure adequate action plans are developed, implemented and evaluated for effectiveness.
Provide R&D Quality & Compliance support for any inspection within region. Participates and/or manages business activities relating to Health Authority inspections/company audits, liaising with other Quality & Compliance organizations as appropriate.
Qualifications
**Required Minimum Education**: Master’s degree in Pharmacy, Chemistry, Engineering or related scientific field.
**Required Years of Related Experience**: 10+ years in a regulated industry. Good knowledge of GMP regulations in Pharmaceutical, Medical Device and Cosmetic product classifications. Minimum of 10 years of Quality experience and 7 years of people management experience.
**Required Knowledge, Skills and Abilities**:
- Experience of the overall product development process.
- Expert knowledge of applicable regulatory requirements (cGMPs) governing various product classification types (OTC, Herbals, Food Supplement, Medical Devices, cosmetic).
- Ability to allocate and balance resources across competing priorities; identify leveraging opportunities and solutions, and mentor others to do the same.
- Ability to provide guidance, collaborate, negotiate, and effectively coach and direct departmental employees and others to ensure an ongoing state of compliance. S
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