R&D Research Associate Cell-line Development

We are looking for candidates with:

• BSc and/or MSc in Biological Sciences, Biotechnology, Molecular Biology, or related disciplines is mandatory. Industry experience is highly desirable.
• Experience in mammalian cell culture, molecular biology techniques, and/or protein production.
• Proven ability to independently execute experimental protocols and interpret data.
• Experience in lab automation setups and GLP environments, with the ability to keep detailed and traceable records on a daily basis.
• Strong ability to work collaboratively within a multidisciplinary group and with external partners.
• Strong data analysis and troubleshooting skills.
• Good communication skills, including the ability to deliver verbal and written scientific presentations.

At HIPRA you will find:

• Continuous learning opportunities.
• A rapidly expanding multinational company.
• A multicultural environment open to new ideas.
• Long-term career opportunities.

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.

The R&D Department at our HIPRA Campus in Aiguaviva (Girona) is actively seeking a highly skilled and driven R&D Research Associate to join our cell line engineering and development team.

The selected candidate will contribute to the development of novel pharmaceuticals for human health, leveraging our state-of-the-art facilities and technologies.

• Execute R&D tasks related to the development of novel pharmaceuticals, including coordination with the rest of the team and collaborators.
• Support the development, review, and optimization of technical plans, as well as contribute to the analysis and discussion of the technical results obtained.
• Ensure the proper maintenance and operation of technical equipment, as well as adherence to pharmaceutical quality standards, including GLP and GMP.
• Maintain accurate experimental records, present findings to project teams, and contribute to the continuous improvement of laboratory workflows.
• Demonstrate effective organization, verbal and written communication skills, and adherence to good documentation practices.
• Author technical reports in compliance with CMC requirements and regulatory expectations.