Job descriptionThe 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. ResponsibilitiesEssential 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. QualificationsRequested skillsMust have: Relevant Life Science / Engineering EducationOngoing or completed university education within pharmacy, biotechnology, chemical engineering, or similar.Must have: Laboratory Experience / Hands-on Practical WorkExperience from laboratory work, sample handling, experimental w…Civilingenjör, bioteknikCell- och molekylärbiologer m.fl.
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