Laboratory Technician

ImmunoIVD is seeking a hands-on Lab Technician with experience in GMP or ISO 13485 environments to join our Operations team. The ideal candidate has a background in molecular biology techniques and a passion for maintaining high-quality standards in a regulated setting. In this role, you will be responsible for performing laboratory-based tasks within Production and Quality Control, ensuring that both production schedules and quality requirements are consistently met.

About ImmunoIVD

ImmunoIVD AB is dedicated to providing reliable, accessible and innovative assays for newborn screening for SCID, SMA and XLA. Our CE IVD marked SPOT-it Screening Kits have been used across Europe since 2018. The assays are highly regarded for their reliability and easy-to-use workflow, requiring minimal laboratory space and equipment investment. We are recognized for our transparent communication and efficient customer support.

Key Responsibilities

• Execute production-related tasks in accordance with Standard Operating Procedures (SOPs).
• Perform quality control (QC) activities following established SOPs.
• Operate dispensing equipment and semi-automated robotic systems as part of the production process.
• Provide support and act as a substitute for other Operations team members when needed.

Qualifications

• Bachelor's degree (BSc) in a scientific discipline or a Biomedical Scientist (BMA) degree.
• Alternatively, experienced technicians trained in molecular biology techniques are also encouraged to apply.
• 1–2 years of industry experience, with a solid understanding of working in compliance with GMP standards.
• Motivated, driven, and humble individual with a proactive attitude.
• Ability to manage multiple tasks effectively, even under pressure.
• Excellent oral and written communication skills in English.

Competence

• Ensures accuracy in documentation, data entry, and experimental execution.
• Skilled in molecular biology techniques, laboratory instrumentation, and process automation tools.
• Understands and consistently applies GMP and QC principles in daily work.
• Works effectively within cross-functional teams and supports colleagues when needed.
• Plans and prioritizes tasks efficiently to meet production and QC timelines.

To apply

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