USP Process Development Senior Scientist
From 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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