Arbetsbeskrivning

This is a full-time consulting assignment where you will be employed by Poolia and work on-site at our client’s facilities in Gothenburg. The assignment is expected to start as soon as possible and will run for approximately 12 months.

About the position

We are currently seeking a highly skilled and motivated Senior Scientist in Analytical Development for a 1-year consultant assignment. In this role, you will be employed by Poolia and assigned to work at one of our clients within the pharmaceutical industry, based in Gothenburg, Sweden. This is an exciting opportunity to work in a highly advanced scientific environment, contributing to the development of innovative medicines that improve patients’ lives.

Reponsibilities

As a Senior Scientist, you will play a key role in analytical development and strategy within drug product projects. Your main responsibilities will include: Contributing to analytical development strategies within cross-functional project teams Performing analytical testing related to drug product characterization and stability Leading and executing method development and validation activities Interpreting and communicating scientific data to stakeholders Supporting Chemistry, Manufacturing and Control (CMC) activities Collaborating closely with formulation scientists, process engineers and other disciplines Identifying, troubleshooting and solving complex technical challenges Ensuring high-quality documentation in line with applicable standards This role includes both hands-on laboratory work and strategic project contributions.

Your profile

To succeed in this role, you are a scientifically driven and collaborative professional with strong analytical expertise and problem-solving skills. We are looking for candidates with: A PhD in Analytical Chemistry or a related scientific discipline, or alternatively an MSc/BSc combined with several years of relevant industry experience Strong expertise in analytical sciences and hands-on experience with techniques such as liquid chromatography (UPLC) Proven experience in method development and validation Strong data analysis skills and ability to interpret and present scientific results Experience in solving technical and analytical challenges Excellent communication skills in English, both written and spoken A proactive and collaborative mindset with the ability to work effectively in cross-functional teams Experience from laboratory-based work It is considered a merit if you have: Experience working in a GMP-regulated environment Knowledge of ELN and LIMS systems Experience with analysis of oral drug products (e.g. dissolution, disintegration, Karl Fischer) Experience with aerosol characterization techniques (e.g. impactor analysis) Experience with analytical methods for biomolecules (e.g. proteins, peptides, oligonucleotides) We review applications on an ongoing basis, so please submit your application as soon as possible.