This is a full time, 1 year Fixed Term Contract, working Monday – Thursday 08:00 – 17:00, Friday 08:00 – 16:00.
As a Method Development & Validation Analyst you will develop and optimise analytical methods along with method validation and transfer according to regulatory guidelines. The role will involve participating in a Professional Scientific Services (PSS) team to ensure the highest quality and productivity standards are met along with the agreed client requirements and timelines.
Job Responsibilities that you be covering:
- You will develop, evaluate and verify analytical methods using a range of techniques, including HPLC and Dissolution, while delivering high-quality analytical testing to support client projects and regulatory requirements.
- You will provide analytical support for technical transfers, method troubleshooting and process development activities, using strong problem-solving skills to drive analytical and process understanding.
- You will review, approve and maintain accurate GMP-compliant documentation, ensuring all records are completed, communicated, filed and managed in accordance with quality and regulatory standards.
- You will support the development of colleagues through training, coaching and knowledge sharing, ensuring all training activities are documented appropriately and completed to the required standards.
- You will collaborate effectively with cross-functional teams, actively participate in team meetings and build strong working relationships to deliver excellent customer service and project outcomes.
- You will work independently and as part of a team, quickly learning new processes, developing practical solutions to challenges and maintaining a highly organised, accurate and quality-focused approach in all activities.