R&D Scientist CDMO

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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 the development of the highest quality innovative vaccines. To give added value to its vaccination experience, the company also develops medical devices and traceability services.

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 Aiguaiviva (Girona)

Initially, the role will focus on providing hands-on technical support across a wide range of activities required to build and operationalize the laboratory, including the implementation of methodologies, installation and qualification of equipment, and establishment of technical capabilities to deliver high-quality CDMO services.

Once the unit is established, the position will evolve to lead and manage biologics development projects for external clients, ensuring the successful execution of development services and acting as a technical point of contact with customers.

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 alternatively 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.

Responsabilities

• Manage multiple projects in parallel within timelines, ensuring that all tasks and responsibilities are carried out according to high scientific standards. Display effective organization, verbal and written communication skills, and adhere to good documentation practices.
• Coordinate the work of laboratory technical staff, specialist technical personnel, or other individuals involved in the project. Additionally, keep the project's technical staff motivated and informed, ensuring their personal and professional development by using appropriate communication channels.
• Participate in the annual budget of the project or projects, and/or technological platform, along with the lead researcher of the project and/or the team leader, and contribute to the monitoring and justification of budget deviations once approved.
• Ensure compliance with Good Laboratory Practices (GLP) in the execution of studies that require them. For studies that do not fall within the scope of GLP, work according to established quality standards.
• Ensure compliance with GMP (Good Manufacturing Process) regulations regarding products, processes, and procedures when applicable, and in any case, work according to established quality standards.
• Collaborate in the development and motivation of the R&D human team, fostering teamwork and professional and personal fulfillment.
• Ensure adherence to pharmaceutical quality standards, including GLP and GMP.
• Stay up-to-date with industry trends and state-of-the-art technologies and contribute to their implementation.
  
  

REASONS TO BE PART OF HIPRA

To be involved in relevant and long-term projects which provide the opportunity to expand knowledge and experience

Growing multinational company with 40 subsidiaries worldwide.

Multicultural environment within the different teamwork.

Promotion of training and development plans.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management, Research, and Science

• Industries

  Motor Vehicle Manufacturing

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