Junior R&D Analyst
The success of a company depends on the passionate people we partner with.
Together, let's share our talents.
As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
Your missions :
Execute, under supervision, the experimental activities related to the development, optimization, and validation of analytical methodologies for veterinary pharmaceutical products, raw materials, and inputs, including forced degradation studies and dissolution profiles.
Support the provision of technical information and technical assistance to R&D, Quality Assurance, and Quality Control areas.
Prepare bench-scale experiments, including sample preparation and analyses for stability studies of veterinary pharmaceutical products.
Perform, under supervision, laboratory experiments to generate technical data, following Good Laboratory Practices (GLP) and ensuring full documentation and traceability of all tests and studies conducted.
Prepare technical documents such as reports, protocols, and analytical methodologies in accordance with technical criteria established by regulatory authorities (MAPA, ANVISA, etc.), official compendia (Brazilian Pharmacopoeia, USP, EP, etc.), and scientific literature.
Contribute and collaborate to project progress, ensuring compliance with scope, timelines, and quality of deliverables.
Actively participate in the investigation and resolution of technical challenges.
Propose continuous improvements in analytical processes and contribute innovative ideas for method optimization and cost reduction.
Contribute to technical knowledge management through the preparation and updating of Standard Operating Procedures (SOPs) and sharing of Good Laboratory Practices.
Follow laboratory and company safety procedures, including the use of collective and personal protective equipment.
Your profile :
Bachelor’s degree in Pharmacy, Chemistry, or Chemical Engineering.
Technical English.
Knowledge of analytical methods and techniques for pharmaceutical products.
Experience in the development and validation of analytical methodologies.
Experience in operating analytical and laboratory equipment.
Experience with software for analytical chromatographs and stability chambers.
Knowledge of technical guidelines and veterinary pharmaceutical regulations (MAPA, ANVISA, VICH, pharmacopoeias, etc.).
