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  1. home
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life scientist

process scientist

helsingborg, skane
posted today
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last day to apply 8 july 2026

job details

last day to apply 8 july 2026

summary

  • helsingborg, skane
  • contingent
  • full-time

posted 17 june 2026

number of offers
1
reference number
JN -062026-609206

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job details

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 ...

th 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.


show more

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.



  • qualification

    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.

  • key responsibilities

    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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