Arbetsbeskrivning

Job description

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.

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.

Qualifications

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.

About the company

Randstad

På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential.

Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.