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87,000+ live jobsR&D Operator
On-site in Paterna·Added 4 months ago (last checked 2 Nov)
61 open roles
Our summary
- Work mode
- On-site, Paterna
- Contract
- Permanent
- Spanish
- Fluent
- Education
- Higher vocational training (FP Grado Superior)




Visa options
The ad doesn’t mention sponsorship
No sponsorship mentioned, and this kind of work is rarely sponsored in Spain.
Skills
Nice to have
This job advert was originally written in Spanish.
Requirements
What we're looking for
- Higher Technician in Manufacturing of Pharmaceutical or Biotechnological Products or related fields.
- Intermediate or Higher Degree in areas related to Laboratory, Analysis, and Quality Control.
- Between 0 and 4 years of experience in a similar position within the pharmaceutical industry.
- Fluent Spanish and intermediate English.
- Knowledge in the preparation and characterization of polymeric solutions.
- Knowledge of analytical techniques such as DSC and SEM.
- Handling of laboratory equipment, materials, and techniques.
- Knowledge of GMPs, SOPs, and basic quality and safety standards applicable to the pharmaceutical environment.
Nice to have
- Training in GMP, pharmaceutical development, and formulation/characterization techniques is highly valued.
- Precision and reliability.
- Attention to detail.
- Innovation, communication, teamwork, adaptability/flexibility, productivity, self-development, sense of urgency, initiative, and proactivity.
Pay & benefits
What you'll get
- 📜 Permanent contract
- 🧪 Joining a pharmaceutical R&D environment
- 🚀 Participation in innovative projects
- 👩🔬 Working in collaboration with technical and scientific teams
- 📚 Opportunities for learning and professional development
The role
Position: R&D Operator
Location: Paterna, Valencia
Experience: 0-4 years
What you'll do
At Bionanopharma, we are looking to hire an R&D Operator to participate in the execution of pharmaceutical trials in bio-lots and batches, as well as in the recording, control, and reporting of results and inventories, ensuring the correct traceability of activities.
The selected person will also collaborate in the cleaning and basic maintenance of equipment and materials, as well as in the training of new hires, following the guidelines defined by the scientific team and complying with standard operating procedures (SOPs) and GMP regulations.
This is an excellent opportunity to develop yourself in a pharmaceutical R&D environment, contributing to the development of innovative solutions and ensuring the proper condition of equipment and materials within the laboratory and pilot plant.
We are looking for a rigorous, proactive person with attention to detail, who wants to develop themselves in the field of pharmaceutical research and development, working in a coordinated manner with technical and scientific teams in a dynamic and innovative environment.
- Execute pharmaceutical trials in bio-lots and batches following the guidelines of the scientific team.
- Record, control, and report results, ensuring the traceability of all activities performed.
- Collaborate in the application of new technologies and development methodologies specific to the Bionanopharma environment.
- Contribute to the optimization of processes, formulations, and trials associated with innovative products.
- Prepare result reports and provide technical support in the interpretation of data derived from pharmaceutical and characterization trials.
- Collaborate on development and scale-up projects.
- Perform cleaning, conditioning, and basic maintenance of equipment, utensils, and laboratory and pilot plant materials.
- Guarantee the correct state of use, availability, and suitability of equipment and materials for development activities.
- Control the inventory of materials, raw materials, and consumables.
- Proactively report replenishment needs to ensure work continuity and the maintenance of required stock.
- Train and accompany new hires in the use of equipment, techniques, and implemented procedures.
- Promote operational standardization, process efficiency, and compliance with quality and safety standards.
- Collaborate with technical and scientific personnel in the preparation, review, and updating of manufacturing guides, procedures, and operating instructions.
- Ensure compliance with SOPs, safety regulations, and quality standards applicable to the pharmaceutical environment.
What do you need? 🤓
- No travel required.
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Hiring process
- Initial contact by the Talent team.
- 1 interview with the Talent team.
- 1 onsite in-person interview.
- Continuous communication during the process.
About Insud Pharma
- Industry
- Pharmaceuticals
In their own words
Additional information
At Bionanopharma, we promote a work environment based on equal opportunity and non-discrimination. All applications will be valued without distinction of gender, identity or gender expression, age, ethnic origin, nationality, religion, sexual orientation, disability, or any other personal, physical, or social condition.
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