GPD Scientist – Consultant Assignment through Poolia

SwedenCompetitive0 applicants

About this role

About the position

This assignment concerns a position as an Analytical Scientist within pharmaceutical development. The work is carried out in a research and development environment with a focus on analytical science related to drug products.

The organization operates across the full development value chain, from early research and development to the production of materials for clinical studies and commercial manufacturing.

The assignment is based in Gothenburg, Sweden.

This is a fixed-term consultant assignment of approximately 12 months. The employee will be employed by Poolia and assigned to work at a client company.

Reponsibilities

The role consists of laboratory-based work within analytical chemistry related to drug products (oral and/or inhaled).

Typical responsibilities include:

Performing analyses for characterization of drug products

Conducting quality control and stability studies

Working with method development and method validation

Documenting experiments and results in accordance with applicable quality standards

Using both manual and automated analytical techniques

Collaborating with cross-functional teams

Your profile

Qualifications (Requirements)

University degree (Bachelor’s or Master’s) in a relevant scientific field

Experience of laboratory work within analytical chemistry

Knowledge of analytical techniques such as liquid chromatography (e.g. UPLC or equivalent)

Ability to document work according to quality requirements

Good collaboration skills

Proficiency in English, both written and spoken

Preferred Qualifications

Experience working in a GMP-regulated environment

Experience in method development, method validation, and stability studies

Experience in analysis of drug products

Experience with statistical or digital tools

Experience in troubleshooting and solving technical challenges

Responsibilities

  • Performing analyses for characterization of drug products
  • Conducting quality control and stability studies
  • Working with method development and method validation
  • Documenting experiments and results in accordance with applicable quality standards
  • Using both manual and automated analytical techniques
  • Collaborating with cross-functional teams
  • University degree (Bachelor’s or Master’s) in a relevant scientific field
  • Experience of laboratory work within analytical chemistry
  • Knowledge of analytical techniques such as liquid chromatography (e.g. UPLC or equivalent)

Requirements

  • Ability to document work according to quality requirements
  • Good collaboration skills
  • Proficiency in English, both written and spoken
  • Experience working in a GMP-regulated environment
  • Experience in method development, method validation, and stability studies
  • Experience in analysis of drug products
  • Experience with statistical or digital tools
  • Experience in troubleshooting and solving technical challenges

EU Requirements

Job Details

Posted28 April 2026
Closes28 May 2026

Contact

Similar Jobs

Finding similar jobs...

GPD Scientist – Consultant Assignment through Poolia at Poolia AB | EuroTalent AI