Validation Project Manager
16 hours ago
Would you like to join an employee-owned multi-disciplinary company specialising in the Life Sciences and Pharmaceutical sectors? Our expertise ranges from design and build contracting and construction management to commissioning and qualification, pharmaceutical validation, and quality consultancy. The Quality Consultancy Services (QCS) team at Scitech work with our clients to help them deliver facilities and equipment that meet the strict regulatory requirements of these industry sectors. **We are looking for**: A Validation Project Manager to lead and manage high value (>1M) qualification projects, or several smaller projects concurrently. Reporting to our Director of Quality and Commissioning Services (QCS), your role will involve building and leading project teams to ensure the proper execution of the Company's business, with emphasis on quality, cost and time compliance while also ensuring contractual, legal & safety, in their projects. As well as managing qualification projects, you will write or review the full qualification lifecycle documents including validation plans, GxP risk assessments, user requirements, design documents, test documents and reports. The Validation Project Manager will implement and maintain suitable project procedures, controls, and records. They will lead project co-ordination and communication processes internally and between the Company, client, suppliers, contractors, statutory bodies, the public and other third parties. **You will have**: - 8 years+ of GxP pharmaceutical, life science or healthcare industry experience, with at least 3 years working as a project manager. - Ideally qualified to degree level or equivalent. - Proven track record in successfully leading project teams, delivering objectives for complex, high value projects. - Strong organisational, communication and management skills with clients, colleagues, and third parties. - Experience of project planning; utilising packages such as MS Project, to define project baselines to effectively monitor, control and forecast project resource requirements and cost. - Working knowledge and practical experience in the management of Regulatory and Quality oriented projects from development of documentation through to execution activities and report development. - Conversant with industry standards such as the Orange Guide and ISPE Guidance documents. Location is not important but flexibility to travel and stay overnight when required is an absolute prerequisite. This role will afford you a degree of autonomy and provide a platform to further develop your career and expertise. **What's in it for you**: A chance to be part of, and share in, our continued success. As an Employee Owner you will, after a qualifying period, be eligible to benefit from a distribution of Scitech's profits. We know how important your professional and career development is and we will work with you to build the skills and knowledge needed to further your career. We believe in rewarding those who share and exemplify our values and deliver for our customers. In short, your success is our success. **Location**: Anywhere in the UK **Hours**: Full time **Contract**: Permanent **Salary**: up to £65,000 (depending on experience) You may also have experience in the following: Validation Team Leader, Project Manager, GMP, Quality Assurance, Qualification, Commissioning, etc. Ref: 133 505
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