Lead the development and implementation of the site R&D strategy including alignment with the site objectives and Global R&D
Responsibility for leading the development, scale-up, registration/validation of drug substance, particle engineering and drug development programs for the site
Promote the scientific excellence and innovation in the area and contribute with technical expertise to expand the Intellectual Property, product and technology portfolios.
Establish the main objectives for the area, aligning these with R&D and company’s corporate strategy
Establish a clear site R&D strategy including resources, capital investment, new technologies etc in order to meet customer and business needs
Ensure the development of safe, efficient, scalable, timely and cost-effective processes of commercial interest to the company
Identify and assess new business opportunities, trends and market needs, in collaboration with commercial colleagues, and ensure the use of up to date / best technology, processes and work practices
Facilitate and manage a culture of innovation within the group focused upon creating new technology value and solving existing technical challenges in alignment with the global R&D strategy
Develop and manage metrics designed to monitor performance and improves efficiencies, quality and HSE culture within the area
Devise and coordinate the implementation of new procedures or the change of existing ones, according to ruling COPs, SOPs and IOPs
Represent the R&D area (or nominate delegates) on meetings with clients, external and internal audits and for Product/Project teams.
Ensure the information flows between the R&D areas, the several internal and external customers and stakeholders
Promote scientific activities (i.e. seminars, congress participations, innovation ideas, papers and publications), innovation and implementation of new methodologies within the R&D area
Manage the R&D team including recruitment, integration, training needs and performance management in accordance with the company’s HR policies and ensuring the team is aligned and motivated towards achieving company’s goals.
Develop and propose for approval the short and mid-term goals, annual budget and budget plan in line with the corporate strategy, in order to align activities with company’s strategic objectives.
Prepare and propose the annual area budget for the annual site R&D budget.
Ensure compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others).
Your Profile
PhD or Masters’ degree in one of the following areas Chemistry, Chemical Engineering, Materials Sciences or related field.
Minimum 8 – 10 years of relevant experience in Research & Development or Manufacturing Sciences in the Pharmaceutical Industry
Demonstrated track record in building R&D capabilities, ideally within in a CDMO environment
Client relationship experience
Possess extensive knowledge of Heat Transfer, Scale-up, Process Safety and Industrial Operations, or of drug product unit operations, solids flow phenomena and process equipment principals and practices, and is able to lead others on them
Good communication skills (verbal and written)
Skilled at driving processes and tools
Fluency in English is a requirement
Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down.