Job Opening
Scientist – Formulation and Process Development
(Fixed-term Project Role)
Are you a bioprocess engineer or formulation scientist passionate about shaping the future of advanced therapeutics? Do you have hands-on experience in developing processes or formulations for new modalities? We are looking for a motivated Scientist to support the maturation of innovative delivery platforms for advanced therapeutics, including viral vectors for vaccines and gene therapies.
ViSync® aims to develop innovative solutions to address the unmet technical needs in new modalities, including the cell and gene therapy sector. The joint venture between Hovione and iBET combined industrial pharmaceutical expertise with cutting-edge biotechnological research in an agile, collaborative environment.
The role is based at ViSync’s site in Oeiras, Portugal, offering an international, multidisciplinary setting at the fore-front of advanced therapeutics development.
This is a full‑time, fixed‑term position (12 months) linked to a defined project focused on the maturation and technical consolidation of ViSync’s viral delivery platforms. The role is intended to support time‑bound experimental, analytical, and documentation activities required to progress selected platforms from exploratory research to a partner‑ready stage within a defined project timeframe.
What you will do
Working within a defined 12‑month project, you will collaborate closely with scientists, project leaders, and technical specialists to support the maturation of ViSync’s viral platforms across internal and collaborative development activities.
You will contribute to the generation and consolidation of experimental data required to support intellectual property protection and platform readiness.
Your role will involve:
- Designing and conducting experiments related to formulation development and particle engineering
- Supporting the generation of structured experimental and analytical data packages
- Analysing and interpreting experimental data to inform project decisions
- Contributing to characterisation, comparability, and stability studies
- Preparing technical documentation and internal reports aligned with future collaborations, grants, or business development activities
You will be part of a cross‑disciplinary, international team working with innovative technologies in a dynamic R&D environment.
Key Responsibilities
- Research & Development
- Contribute to the optimization and technical consolidation of viral delivery platforms for advanced therapeutics.
- Execute experimental plans and analyse data supporting platform characterization and readiness.
- Innovation & Expertise
- Apply formulation and bioprocess knowledge to support scalable and robust delivery solutions.
- Contribute scientific insight to evolving R&D workflows and platform strategy.
- Project Support
- Collaborate with cross-functional teams to ensure timely delivery of project objectives.
- Provide technical input to support risk identification and decision‑making within the defined project scope.
- Documentation & Communication
- Document experimental work in lab notebooks and technical reports.
- Support the preparation of structured data packages and technical documentation.
- Present results to internal teams and external collaborators, and contribute to scientific discussions.
- Compliance & Quality
- Ensure all laboratory activities comply with GLP, HSE, and applicable regulatory standards.
- Support quality and audit-readiness as required.
- Funding & Collaboration
- Contribute technical content to collaborative initiatives and grant-related activities, where relevant.
- Demonstrate flexibility in supporting multiple workstreams within the defined project scope.
Education / Qualification
Master’s degree (or equivalent) in Chemistry, Biochemistry, Physical Chemistry, Pharmaceutical Technology, Biotechnology, Biological Engineering, Biology, or a related field. A PhD is a strong advantage, but not essential.
Experience
Minimum 2 years of relevant experience in Research & Development, ideally within the pharmaceutical, biotechnology, CRO/CDMO industry, or academia. Experience in formulation development, bioprocessing, or advanced drug delivery systems is highly desirable. Familiarity with working in cross-functional teams and contributing to project execution is a plus.
Technical Competencies
- Experience or strong interest in viral vector technologies and advanced therapeutics.
- Background in formulation development and/or analytical characterisation is a plus.
- Ability to work autonomously in a dynamic, fast-paced, project‑driven environment.
- Strong data analysis, interpretation, and scientific communication skills.
- Proficiency in MS Office and familiarity with data analysis tools (e.g., Power BI, GraphPad Prism). Experience with statistical analysis or machine learning is a plus.
- Knowledge of GLP, regulatory compliance, and industry standards for advanced therapeutics.
So, what’s next?
Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you!
Please send us your application, including your CV and a Cover letter no later than 30th of April 2026 to this email with the subject [ViSync Scientist 2026 – APPLICATION].
Applications will be reviewed on a rolling basis, and interviews may be conducted as candidates apply. The position may be filled before the advertised deadline once a suitable candidate is identified.
For more information about the position, please send us an email with the subject [ViSync Scientist 2026 – QUERY]
We value your privacy and are committed to protecting your personal data. Your information will be used solely for evaluating your application and shared only with our recruitment panel. By submitting your application, you consent to this process. Thank you for considering a career with us.
Equal Opportunity Employer
ViSync® is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.