Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. Role Overview In this role you will manage a group of Analytical leader(s) and Analytical Chemists in a cGMP laboratory environment, supporting customer funded product development, Kindeva Analytical Services and internal self-funded projects. Key Responsibilities Include, But Are Not Limited To Direct the activities of the function to achieve operational effectiveness. Cascade functional strategy through the team, to deliver testing data and documentation that meet project quality and compliance expectations. Strategic planning of analytical and development objectives, participating with senior management and other functional key stakeholders. Participate in global budget planning, focusing on/responsible for spending, through planning, to adhere to the functional budget (direct/ indirect expense and CAPEX). Support strategic planning and development of new business, providing technical specialist direction and work plan estimates, for new and existing projects/customers. Allocate analytical resources (people, materials, and budget) as necessary to achieve goals and project/customer timelines. Ensure all areas of analytical (labs, offices, and other facilities) and staff are safe, compliant and inspection ready always. To be a subject matter expert both internally and in discussions with customers and potential partners. Interact and participate with management at all levels and customers to agree/negotiate plans to win and deliver business results. Contribute to the development of staff and ensure analytical staff have training appropriate for their responsibilities and their career growth/development. Be a mentor to all members of the analytical team. Accountable for the delivery of project work to meet the business objectives. Significant capability/awareness and understanding of a broad range of analytical techniques. Responsible for ensuring that evolving regulatory requirements are incorporated into the procedures and practices executed in the analytical lab. Conference podium/poster presentations, not essential but preferred. Skills & Experience Qualified to PhD degree level with 8 years’ experience / MSc degree level with 10 years’ experience or 20 years’ qualified by experience. Analytical and managerial experience/competence demonstrated. Proven experience leading and mentoring scientific teams, including performance management and professional development. Supervisory experience in a pharmaceutical lab environment, with experience of inhaled medicines preferred. Technical capability to shape departmental strategies for method development and method validation. Demonstrated cross-functional interactions, preferably at a Global level. Key Capabilities Inspire and motivate your team to achieve excellence and accountability. Lead by example with integrity, professionalism, and scientific accuracy. Excellent interpersonal skills, both written & oral. Strong verbal communication skills, especially in cross-functional/leadership meetings. Adapt to changing priorities, timelines, and regulatory expectations without compromising on quality. Demonstrate strong analytical and decision-making skills. Use data to guide actions and continuously improves processes. Maintains a high standard of accuracy, completeness, and documentation. Champion data integrity and encourage a right first-time culture. What We Offer Attractive compensation package. Company pension scheme (up to 10% employer contribution). 25 days holiday per year (plus bank holidays) plus service days after 5 years. Private Medical Insurance. Company sick pay. Employee Assistance Program with 24/7 confidential helpline support for employee and immediate family. Life assurance of four times life cover salary. Flexible working hours. Wellness programmes. Employee recognition program. Employee development. Free on-site parking. Discount and cashback at many retailers. Cycle to work scheme. Flu vaccinations. Employee referral scheme. Additional Information Working Hours: 37.5hrs per week Location: Charnwood Campus, Loughborough All applicants must be eligible to work in the UK. We believe our people make the difference at Kindeva, we look for skilled, passionate, and driven professionals to come and work with us to help us excel in manufacturing technologies and processes, which bring lifesaving products to patients worldwide. Apply Now