
Quality Lead RP Durbin Ireland
- Ireland
- Permanent
- Full-time
- Responsible Person will be responsible for the compliant management of Durbin Ireland WDA and all associated GxP and Medical Device activities
- Perform all activities in compliance with Uniphar Group Policies and Procedures.
- Liaise and lead regulatory and client inspection activities as required.
- Work with the EAP Quality Lead to ensure processes and procedures are effectively documented.
- Project manage and schedule key projects and initiatives insuring timely execution and goal achievement.
- Implement and ensure compliance to the quality requirements as per Quality Management system.
- Develop staff on new quality initiatives and assist in the understanding and rollout of quality initiatives across the department/site.
- Ensure development and maintenance of Regulatory standards and procedures in accordance with all applicable Regulatory regulations, guidance, and specifications.
- Identifies regulatory system enhancement needs or technical issues and works closely with systems and technical support staff to identify, develop, and implement solutions.
- Analyse audit results and make recommendations to management on areas that may require additional staff training, improved documentation or process improvement in order to remain compliant with regulatory standards
- Effectively manage large amounts of information and documentation.
- Review requirements to provide feedback on completeness, evaluation and other risk areas that could impact quality compliance.
- Contribute to the development of high-quality systems by ensuring functionality meets documented specifications, quality requirements and organisational goals.
- Lead issue triage and resolution meetings with internal & external departments.
- Build strong relationships with business and diverse stakeholders and champion continuous improvement initiatives across the business.
- Prepare, distribute, and maintain weekly & monthly reports/KPIs summarising information regarding all the above
- Participating in continuing own and team professional development to maintain awareness in current and new regulations and ensuring new regulations are implemented
- Responsible for the management of providers and processes for any outsourced GMP activity
- Other projects as assigned by management
- 3 to 5 years of work experience in a regulated industry (GDP/GMP/ Unlicensed Medicines)
- Previous experience in regulatory authority inspections
- Must have ability to lead and develop a small team of people.
- Excellent communication skills and the ability to work well with people at all levels are essential.
- Must have strong organisational, analytical, problem solving, influencing and management skills.
- Project management experience is a plus.
- Knowledge and experience with software including word processing, spreadsheets, and statistical analysis.
- Ability to work in a fast-paced team environment, effective decision-making, and problem-solving skills
- Proven time management and prioritisation skills focusing on urgent and overlapping deadlines
- Strong organisational skills, attention to detail and proven accuracy with record keeping
- Ability to work independently
- Experience of Validation methodologies
- Commercial acumen
- Bachelor’s degree in science/engineering related field preferred
- Positive can-do attitude with a focus on action does not debate.
- Results orientated.
- Pursues a standard of excellence, relentlessly measuring and chasing to ensure targets met.
- Resolves conflict constructively and works well under pressure.
- Attention to detail.
- Strong communication and negotiation skills.