R&D Scientist CDMO

HIPRA; Aiguaviva; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

HIPRA, a leading pharmaceutical and biotechnological company, is seeking an R&D Scientist CDMO to support the launch of a new R&D unit. The role involves providing technical support, managing biologics development projects, and ensuring compliance with quality standards in a dynamic team environment.

Servicios

Participation in long-term projects

Support for training and professional development plans

Multicultural work environment

Formación

• At least 1 year of industrial experience in biologics production or at least 3 years without a Ph.D.
• Hands-on expertise in lab and pilot-scale operations: bioreactors, filtration, chromatography, analytics.
• Familiarity with GMP principles and quality systems for biologics development.

Responsabilidades

• Manage multiple projects in parallel within timelines, ensuring high scientific standards.
• Coordinate the work of laboratory technical staff and other personnel involved in projects.
• Ensure compliance with GLP in studies requiring it, and adhere to established quality standards.

Conocimientos

Problem-solving

Communication

Teamwork

Educación

Ph.D. in Biotechnology, Bioengineering, Pharmacy, or related field

Herramientas

ELN

QMS

Data analysis tools

Descripción del empleo

HIPRA is a pharmaceutical and biotechnological company focused on prevention and diagnosis for animal and human health, with a broad range of highly innovative vaccines and an advanced diagnostic service.

HIPRA has a solid international presence in more than 40 countries, with its own subsidiaries, 11 diagnostic centres, and 6 production plants strategically located in Europe (Spain) and America (Brazil). Research and Development constitute the core of its knowledge.

HIPRA dedicates 15% of its annual turnover to R&D activities that concentrate on the creation and application of the latest scientific advances to develop high-quality innovative vaccines. The company also develops medical devices and traceability services to add value to its vaccination experience.

At HIPRA Biotech Services, we are seeking an R&D Scientist CDMO to contribute to the launch and consolidation of our newly created R&D CDMO unit, a dedicated team established to provide Cell Line Development, Process Development, and Analytical Development services to external clients.

This position is based in Aiguaviva (Girona). Initially, the role will focus on providing hands-on technical support across activities required to build and operationalize the laboratory, including methodology implementation, equipment installation and qualification, and establishing technical capabilities to deliver high-quality CDMO services.

Once established, the role will evolve to lead and manage biologics development projects for external clients, ensuring successful execution and acting as a technical point of contact.

Qualifications

• Ph.D. in Biotechnology, Bioengineering, Pharmacy, or related field with at least 1 year of industrial experience in biologics production (mammalian and/or microbial), or at least 3 years of equivalent experience without a Ph.D.
• Practical experience in bioprocess development, scale-up, and tech transfer for biologics (monoclonal antibodies, recombinant proteins, enzymes, etc.) using mammalian and/or microbial systems.
• Hands-on expertise in lab and pilot-scale operations: bioreactors, filtration, chromatography, analytics.
• Prior experience in a CDMO environment is a plus.
• Proven ability to prepare and manage technical documentation and communicate results to clients is a plus.
• Experience interacting with clients, including technical meetings, presentations, and lab visits, is a plus.
• Familiarity with GMP principles and quality systems for biologics development.
• Experience with ELN, QMS, and data analysis tools is desirable.
• Strong problem-solving, communication, and teamwork skills; ability to manage multiple projects and priorities.
• Fluent in written and spoken English.

We are looking for a proactive, flexible, solution-oriented individual with a multidisciplinary mindset, capable of adapting to the evolving needs of this new and dynamic unit, collaborating effectively across functions, and contributing both technically and strategically to the team’s success.

Responsibilities

• Manage multiple projects in parallel within timelines, ensuring high scientific standards, effective organization, and good documentation practices.
• Coordinate the work of laboratory technical staff and other personnel involved in projects, maintaining motivation and professional development.
• Participate in the annual budget planning and monitor project or platform expenses, contributing to the justification of deviations.
• Ensure compliance with GLP in studies requiring it, and adhere to established quality standards for non-GLP studies.
• Ensure GMP compliance regarding products, processes, and procedures when applicable.
• Contribute to the development and motivation of the R&D team, fostering teamwork and growth.
• Stay updated with industry trends and technologies, contributing to their implementation.

Reasons to Join HIPRA

• Participation in relevant, long-term projects to expand knowledge and experience.
• Growing multinational company with 40 subsidiaries worldwide.
• Multicultural work environment.
• Support for training and professional development plans.