Specialista In Ricerca E Sviluppo Bardi

Specialista In Ricerca E Sviluppo
Bardi
Emilia Romagna, Bardi

NerPharMa operates as a CDMO (Contract Development and Manufacturing Organization) and offers unparalleled expertise in bringing highly potent compounds to the marketplace. NerPharMa has brought new products and unique innovative technologies to the market over the years, delivering a wide range of GMP services through its agile and flexible facilities. NerPharMa owns a wide and cutting-edge organizational structure able to manage and handle highly active compounds, and to ensure the full development and production of active principles and finished products intended for the world market as well as the research and development of innovative formulation and delivery systems. About the position: R&D Formulation Expert Reporting to the Head of R&D, the candidate will be in charge of formulation development of oral solid and injectable drug products from lab to industrial scale, including batches intended for clinical trials. He/She will act under the supervision of the Formulation Lead and should be self-motivated, possess good interpersonal skills, and have the ability to independently handle a diverse workload of projects. Key Responsibilities: Planning and executing formulation development studies aimed at the manufacturing of solid oral forms or injectable solutions defined by the customers Preparing protocols, reports and other associated project / GMP documentation that are required to fulfil the projects or department's needs Ensuring that laboratory equipment remains in good state and functions as required Collaborating with Project Management functions in project activities such as formulation development or technology transfers Collaborating with Production, Quality and Regulatory functions in product scale-up activities from the lab phase to the industrial phase Assisting the Head of R&D with technical assessments for quotations and support any Business Development activities that are required Complying with the policies, procedures, and regulations in place in the company Contributing, together with his/her supervisor, to the fulfilment of the obligations provided for the protection of health and safety in the workplace Qualifications & Experience: Master's Degree required in Chemistry, Pharmaceutical Sciences or a related scientific field. PhD Degree is highly recommended Minimum experience of at least 5 years in a similar role in companies in the pharmaceutical sector Experience in handling high potent drugs Biologics and biotechnology formulation development experience Working knowledge of mixers, tablet presses, granulators, pans, fluid beds and capsule filling machines Knowledge of DOE techniques applied to formulation development is highly recommended Predisposition to order and precision Very good knowledge of English, written and oral He/She must exhibit good writing, communication and time-management skills and be proficient in Microsoft Word, Excel, Outlook, and similar programs. Ability and willingness to work in a team environment and participate in team activities is a must. Seniority level Mid-Senior level Employment type Full-time Job function Research and Manufacturing Industries Pharmaceutical Manufacturing J-18808-Ljbffr