publicerad 17 juni 2026
The overall purpose of the role is to support pilot plant activities connected to clinical & stability batches, laboratory work, process development and documentation in a GMP-regulated environment.
Essential duties and responsibilities:
•Support preparation and execution of clinical, pilot and development batches in accordance wi ...
•Perform hands-on laboratory and pilot plant work, including material handling, sample preparation and documentation.
•Support process development, technical evaluations and troubleshooting activities.
•Document work in protocols, batch records, reports and/or relevant quality systems.
•Collaborate with R&D, Quality, QC, Production and other internal functions.
•Participate in investigations, deviation handling and improvement activities when relevant.
The overall purpose of the role is to support pilot plant activities connected to clinical & stability batches, laboratory work, process development and documentation in a GMP-regulated environment.
Essential duties and responsibilities:
•Support preparation and execution of clinical, pilot and development batches in accordance with established instructions and procedures.
•Perform hands-on laboratory and pilot plant work, including material handling, sample preparation and documentation.
•Support process development, technical evaluations and troubleshooting activities.
•Document work in protocols, batch records, reports and/or relevant quality systems.
•Collaborate with R&D, Quality, QC, Production and other internal functions.
•Participate in investigations, deviation handling and improvement activities when relevant.
Requested skills
Must have: Relevant Life Science / Engineering Education
Ongoing or completed university education within pharmacy, biotechnology, chemical engineering, or similar.
Must have: Laboratory Experience / Hands-on Practical Work
Experience from laboratory work, sample handling, experimental work, preparation of materials or other practical technical/scientific tasks.
Must have: Quality Mindset & Attention to Detail
Structured and accurate way of working, with an understanding of the importance of quality, traceability and documentation in regulated environments.
Must have: Problem-Solving & Analytical Skills
Interest in understanding technical processes, evaluating results and contributing to practical solutions and continuous improvements.
Must have: Swedish and English Language Skills
Good communication skills in Swedish and English, both written and spoken.
Good to have: GMP / QA / QC Understanding
Experience or understanding of GMP, quality assurance, quality control, deviation handling, regulated documentation or quality systems.
Good to have: Pharmaceutical / Biotech / Medtech Environment Exposure
Previous exposure to pharmaceutical, biotech, medtech, laboratory, pharmacy or other regulated life science environments.
Good to have: Analytical Methods / Sample Handling
Experience from analytical laboratory work, sample preparation, material handling, material characterisation such particle size distribution, morphology, flowability, disintegration, viscosity etc.
Good to have: Process Development / Process Workflow Interest
Interest in process understanding, troubleshooting, process improvement or working close to the transition between development and production.
Good to have: Independent & Collaborative Work Style
Ability to take responsibility for assigned tasks, work proactively and collaborate with different internal functions.
Essential knowledge and skills:
Basic understanding of laboratory work, structured documentation and working according to established procedures.
Interest in GMP-regulated environments, pharmaceutical manufacturing, process development and technical problem-solving.
Core competencies required for this role:
•Strong analytical, communication and collaboration skills.
•Structured and quality-conscious way of working.
•Independent thinking and good planning/prioritization skills.
•Highly motivated self-starter who takes accountability for assigned tasks.
•High degree of accuracy, quality and attention to detail.
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