Specialista In Ricerca E Sviluppo Milano

Specialista In Ricerca E Sviluppo
Milano
Lombardia, Milano

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 ExpertReporting 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 customersPreparing protocols, reports and other associated project / GMP documentation that are required to fulfil the projects or department's needsEnsuring that laboratory equipment remains in good state and functions as requiredCollaborating with Project Management functions in project activities such as formulation development or technology transfersCollaborating with Production, Quality and Regulatory functions in product scale-up activities from the lab phase to the industrial phaseAssisting the Head of R&D with technical assessments for quotations and support any Business Development activities that are requiredComplying with the policies, procedures, and regulations in place in the companyContributing, together with his/her supervisor, to the fulfilment of the obligations provided for the protection of health and safety in the workplaceQualifications & Experience:Master's Degree required in Chemistry, Pharmaceutical Sciences or a related scientific field.

PhD Degree is highly recommendedMinimum experience of at least 5 years in a similar role in companies in the pharmaceutical sectorExperience in handling high potent drugsBiologics and biotechnology formulation development experienceWorking knowledge of mixers, tablet presses, granulators, pans, fluid beds and capsule filling machinesKnowledge of DOE techniques applied to formulation development is highly recommendedPredisposition to order and precisionVery good knowledge of English, written and oralHe/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 levelEmployment type Full-timeJob function Research and ManufacturingIndustries Pharmaceutical Manufacturing#J-18808-Ljbffr