Want a 3D Career? Join Norgine. At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community. We call it the 3D career at Norgine and it offers you a fully-rounded experience with no limits. Bring everything about yourself that you’re proud of, whether that’s your passion for making a difference, focus on others’ well-being, or intellectual curiosity to unleash in a fast-paced environment and supportive community. In return, get a sense of belonging, a long-term career with ongoing development and upskilling, and a company that cares about people’s wellness as much as you do. Because at Norgine, we transform lives with innovative healthcare solutions. We have an exciting opportunity for a CSV Analyst to join Norgine. The person holding this position will report to the Head of IT. This role is responsible for ensuring that Norgine IT Quality Management System, Validation documentation and all related processes, procedures and systems meet the requirements of all applicable regulations. This means not only working with other team members and consultants to identify any such weaknesses but also being instrumental in closing any such gaps identified. This may involve both directing others regarding what is needed and also making such changes themselves. This is a 12 months FTC role. If you want a multi-dimensional 3D career in a leading healthcare organisation, join us. Requirements KEY RESPONSIBILITIES • Assist the CSV/Lead Process Analyst in continued improvement and delivery of the Global IT validation strategy and approach taking into account the relevant GxP requirements (e.g. EU Annex 11, FDA 21 CFR Part 11, Part 820, etc.) and also other relevant regulatory requirements • Support the continuous improvement of appropriate procedures to be used in validating computerized systems: Develop, review and approve CSV policies, procedures, plans and protocols, and champion their adoption. Support project teams in defining the appropriate level of validation required based on a risk assessment Support project teams in the creation of the agreed validation pack of documents to support the validated state • Support the business functions in the periodic review of systems to assess the current validated state • Acts as a quality contact and primary Subject Matter Expert (SME) for Computer System Validation (CSV) and Risk Management • Review proposed changes to validated computerized systems and identify the validation requirements necessary to maintain the system’s validation status after execution of the change. • Support project teams in the assessment of proposed new computerized systems or software for GxP impact and where GxP impact is identified provide guidance on the risk based validation approach for the system, working with key stakeholders to achieve business goals. • Support formal testing of computerized systems ensuring that test plans, test scripts and test results comply with the regulatory requirements based on system risk. • Ensure that the Local Validation Master Plan is maintained and is aligned to corporate policies as they relate to computer systems validation • Assists in all forms of audit and responds to audit observations and corrective actions as they pertain to computer systems validation • Interacts professionally with company management, internal departments and other areas of the business to effectively implement and maintain Quality Systems as they relate to CSV • Identifies and implements improvement opportunities with the CSV/Lead process Analyst for established Quality Systems, processes, procedures, and training to support IT CSV activities • Maintain up to date knowledge of evolving regulatory requirements, availability of current/new techniques, and literature regarding compliant computer operations, and act as an information resource for the team and wider business. • Such other activities as may be necessary from time to time Education and experience • Bachelor’s degree preferred • Experience in a validation and qualification of complex computer systems • Thorough knowledge of cGMP regulations related to CSV • Good written and oral communication skills • Competent user of Microsoft Office T echnical Skills • Familiarity with multiple system types such as ERP and BI, LIMS, HRIS etc. • Good understanding of business requirements, high-level solutions and infrastructure components, combined with CSV system experience. • Wide experience of the various regulatory requirements relating to Eudralex Annexe 11, FDA CFR21 Part 11, etc • Experience of the data integrity implications of the regulated environment Team Skills • Confident communicator, able to network effectively in a diverse business community. • Proactive, professional approach, undertakes tasks and responds to business requests in a positive and constructive manner. • Keeps industry and organization knowledge current in order to provide up to date solutions and be best placed to advise on future capabilities. Benefits Our benefits may vary per location. Please liaise with the Norgine TA representative to obtain more information. Sound good? Find out more about the career you’ll have with Norgine, then apply here. LI-PP1