Description
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: October 22, 2024
Consultant: Paula Crespo