USP Process Development Senior ScientistFrom Robert Walters, we are looking for a creative, organized and open-minded USP Senior Scientist to lead and execute process development programs at lab scale and pilot scale manufacturing batches for biopharmaceutical products (including recombinant proteins and mRNA-based therapies). If you are interested in developing your career as a USP Process Development Senior Scientist in a pioneering and innovative CDMO start-up located in Barcelona, don't hesitate to apply!
Minimum Requirements: Background in Biomedical sciences / Pharma / Biotech.At least 5 years experience in the biotechnology industry.Deep knowledge in upstream processes with different expression platforms (bacterial, yeast, cell culture).Expertise in working with stainless-steel and single-use stirred tank bioreactors.Practical experience in aseptic techniques, cell culture, single-use bioreactors (SUBs), wave reactors, and harvest/clarification processes.Knowledge of GMP and ICH regulatory guidelines is a plus.Nucleic acids knowledge is a plus.Able to work in a cross-functional approach and work independently with minimal supervision.Ability to function in a constantly evolving environment & prioritize multiple tasks.Team player in an evolving environment.Strong interpersonal and communication skills; written and oral.Based in the Barcelona Area.Tasks and Responsibilities: Take the lead in assigned project development (development plan and design of experiments).Lead and execute process development programs at lab scale and pilot scale manufacturing batches.Author required technical documentation (reports, batch record documents, SOPs, etc.).Critically evaluate experimental results and suggest following activities.Create technical proposals for scale-up and scale-down processes.Participate in lab management tasks.Responsible for the performance of the operational activities to the required quality and on time according to project timelines.Responsible for reporting the results according to company documentation standards.Work under SOP procedures at expected quality standards.Flexible schedule, depending on process activities.Opportunities for professional development and growth.Participate in the expected growth of the process department in the near future.Opportunity to work in a dynamic and challenging environment.Opportunity to work in a biopharma CDMO located in the Barcelona area, with multiple products/projects ongoing and perspectives for market approval of several products.Contract Type: FULL_TIME
Specialization: Pharma, Healthcare & Biotech
Area: Medical R&D
Sector: Pharmacy
Salary Band: Negotiable
Job Type: In-person
Experience Level: Associate
Location: Barcelona
Reference: 2268422/001
Publication Date: 22 de octubre de 2024
Consultant: Paula Crespo
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