Method Development & Validation Analyst

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.
What skills, qualifications and experiences you will hold as a Method Development & Validation Analyst:
You will hold an Honours Degree in Analytical Chemistry or a related scientific discipline, with a strong scientific foundation and the ability to apply technical knowledge within a regulated laboratory environment.
You will have extensive experience in analytical method development, method validation and lifecycle management, with a strong understanding of current industry and regulatory expectations.
You will have hands-on experience using HPLC and Dissolution techniques, supported by significant analytical testing and validation expertise within a GMP-regulated environment.
You will have a thorough understanding of GMP requirements and ICH guidelines, with the ability to ensure compliance whilst maintaining high standards of quality and data integrity.
You will have excellent planning, organisational, communication and documentation skills, with strong attention to detail and the ability to manage multiple priorities effectively.
You will have strong IT skills and a flexible, collaborative approach, enabling you to work effectively as part of a team, adapt to changing business needs and drive continuous improvement initiatives.

Employment type
Full-time

Work arrangement
No