Description JOB OVERVIEW Primary technical contact for client communication. Execute projects to support formulation development, tech transfer, scientific data analysis, registration batches or clinical trials manufacture. Maintain systems and facilities in a cGMP status and manufacture supplies in a compliant manner. Generate data and reports to support product development, validation or registration in a compliant manner. Secondary SME for regulatory and customer audits as well as technical meetings on clinical trials, formulation or tech transfer manufacturing at Morpeth. KEY RESPONSIBILITIES Primary product development person for Piramal projects. Co-ordinate with Project management in the execution of development projects. Co-ordinate with Production groups for the introduction of new products. Maintain the department facilities, records, equipment and procedures in line with GMP. To develop skills and knowledge relevant to the operations. Maintain the departmental compliance to GMP and procedures for operation of rooms and equipment, record keeping and reports. To conduct experiments which increase the company understanding of products it manufactures or intends to manufacture. Responsible to ensure that R&D activities comply with QMS and EHS requirements. Managing and protecting R&D assets as intellectual property. Budgeting and managing expenses Develops strong, collaborative relationships with other departments/groups and fosters an environment of knowledge sharing and cross-functional teamwork. Keeps up to date with current trends and advances in Pharmaceutical sciences for oral dosage forms. Qualifications ESSENTIAL QUALIFICATIONS AND SKILLS: Degree in Pharmacy or Chemistry, (Ph.D desirable). Excellent written and oral communication skills. Results oriented Driven and accountable, Collaborative and transparent, Strong hands-on, “roll up your sleeves” approach to tasks, Ability to think strategically and execute on strategy, RELEVANT EXPERIENCE: Significant experience in formulations development or processing pharmaceutical products. Experience in development of generics products and Quality by Design principles is desirable.