Site Quality Manager
Rpg Recruitment Ltd
Waterford, Tipperary
Site Quality Manager. Excellent role for a site Quality Manager for an FDA pharmaceutical company based Co Waterford. Reporting to the Managing Director with dotted line to Head of Quality UK & IE, the Purpose of this role is To provide a professional and technical leadership to the Site and work in conjunction with sister Sites to establish and maintain regulatory compliant quality systems to ensure that all products are manufactured and distributed in compliance with Group, Company, Contract Client, Regulatory and Safety Standards. Responsibilities Include:- Provide a full technical leadership to the Irish sites, building a technical team who are capable and have a solid understanding of Quality Assurance, Control, Validation, Stability and Microbiology functions. As person named (QP) on the company’s manufacturing authorisation, the job holder is personally and professionally accountable for the quality of all products released for sale. Identify and implement process changes to improve product quality and/or reduce processing costs. Assess and resolve any technical issues to ensure appropriate timely solutions are delivered in line with industry standards ensuring effective corrective and preventative actions are instigated. Improve efficiency in QA/QC operations utilising tools such as Lean systems. Delivery of short and long term Quality operations targets. Definition and delivery of Quality strategy. Effective direction, management and development of the Quality team in support of the business as a whole. Senior level contribution to general direction and management of the business as a whole. Lead role with regulatory bodies during company audits. To foster excellent communication between all business functions, both internally and externally. Work together with other sites Quality functions on harmonisation of standards and best practice across the Organisation. Key responsibilities listed above are not exhaustive and may vary depending on the demands. Requirements:- The ideal candidate will have. Minimum of a level 8 degree in a science discipline. Must hold “Qualified Person” Status. A min of 5 years experience leading a team in a manufacturing pharmaceutical environment with Strong leadership skills in managing a team. Have an ability to manage the process of innovative change effectively. Remains on the forefront of emerging industry practices. Be excellent in Solution Development and Delivery: d) Technical Expertise: Is a Qualified Person and maintains and updates knowledge and expertise to ensure the technical function maintains best practice. Have strong communication skills. Demonstrated Continuous Improvement in past experience. This job originally appeared on RecruitIreland.com.
2051 days ago