About the job Veranova is seeking a highly skilled and motivated Team Leader with extensive experience in small molecule organic chemistry and kilo-laboratory scale production to join our Process Research & Development group. The position requires an in-depth understanding of the field of synthetic organic chemistry including process development and the transfer to kilo-scale production. The Team Leader will be responsible leading all aspects of development and production programs from early phase development through scale up to manufacture. Success will require effective leadership to oversee and manage the progress and performance of more junior staff and serve as the primary client contact and lead scientist for multiple projects. The preferred candidate will have previous experience with the development and large-scale production of small molecule API targets in the pharmaceutical industry. Expertise in organic chemistry, analytical techniques and strategies commonly used in the development of these types of molecules is essential. Knowledge of cGMP and regulatory guidelines is preferred. The Company We are a global leader in the development and manufacturing of active pharmaceutical ingredients, with expertise in highly regulated and complex chemistries. We have over 50 years of experience navigating the challenges of the global healthcare industry, and nurturing long-standing, trusted customer relationships. Operating within two divisions, Generics and Originators, we deliver a differentiated service offering to pharma and biotech customers for every stage in the drug development lifecycle. Key responsibilities In this role you will be responsible for: Design and implement methods to enable the synthesis, purification, isolation, and scale-up of drug molecules. Maintain, build and manage the operations of a kilo-scale production laboratory at up to 100 L scale. Exhibit a high level of safety awareness and conduct lab operations in a safe manner as well as hold others accountable for safe behavior in the work environment. Mentor, lead, and advise junior scientists in areas of scientific, regulatory, project management, client, and safety issues. Create detailed work plans to meet project goals within the required timeline and budget. Responsible for internal and external technology transfer of processes to kilo lab and pilot plant manufacturing at other site facilities. Work globally with both internal and external development teams and interface cross functionally. Drive continuous improvement to enable improved process understanding to ensure ‘right first time’ operation of processes. Recommend potential courses of action to senior management by providing solid results, findings, and technical solutions to project issues and day to day problems. Keep accurate, legible, and complete records of all experiments and observations. Generate written progress reports and clearly present scientific results to clients and management. Multi-task responsibilities including laboratory work, preparing scientific reports and documents, presenting scientific findings to clients and management, and using scientific literature to solve advanced technical problems. Share special skills and expertise with other team members and departments such as Analytical Development, Quality Control, Quality Assurance, and Production groups. Other duties as assigned. Special Factors Required to work to regulatory and safety standards Responsible for contributing to audit readiness and for participating in audits with regulatory agencies, internal compliance audits and customers, as needed. What you need for the role To succeed in this role you will have; Ph.D. in chemistry, chemical engineering, or related field. 5 years of direct work experience in the pharmaceutical industry in a Senior Scientist role Knowledge and experience of scaling chemistry to kilo scale manufacturing. Broad experience with proven accomplishments in organic chemistry including small-scale and large-scale preparation of drug substances and intermediates. Experience in leading multiple projects by providing direction to various levels of laboratory personnel and oversee production programs. Ability to successfully work with interdepartmental teams. Understanding of process safety concepts and how to incorporate them into process development plans to ensure processes are safe upon scale up. Knowledge of analytical techniques specifically with respect to in process analysis of peptide reactions and to analysis of isolated intermediates and products. Demonstrated ability to exercise good judgment and make decisions in a timely manner. Experience working in a cGMP production environment. Expertise in the use of statistical methods such as design of experiments (DoE). Experience with Microsoft Software programs Strong written and verbal scientific presentation skills. How will you be rewarded The company provides an industry leading compensation package, and this position is eligible for an annual performance bonus in accordance with the terms of the applicable bonus plan. You will also receive excellent pension contributions, life insurance and receive 25 days annual leave plus public holidays. Employees will also be eligible to participate in a health cash plan, savings plan, Cycle2Work scheme, technology savings and enhanced family friendly polices to help support our people during important, life changing moments. At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career. If you have the necessary skills and experience to join our team, please apply online. For any queries or should you require any reasonable adjustments to support your application please let your recruiter know when they contact you. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice. Veranova is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.