Downstream Peptide Technician – GMP Cleanroom

Carbosynth LLC; Lelystad; On-site; EUR 34,000 - 42,000; Full time

Job summary

Biosynth Netherlands is seeking a Laboratory Technician to support downstream peptide production in a cleanroom environment. You will perform purification, lyophilization and sample analysis, working closely with other peptide technicians to ensure timely delivery of materials.

Responsibilities include operating purification equipment, maintaining records, and complying with ISO 9001 and GMP-API where applicable. A hands-on, detail-oriented team player with lab experience is preferred.

Qualifications

• MBO or HBO professional education in related field (e.g., chemistry or equivalent).
• Good practical and theoretical knowledge of relevant discipline.
• Experience working in lab environments preferred.

Responsibilities

• Execute lab activities related to projects in downstream production.
• Daily tracking and record keeping of peptide tasks/projects.
• Process and execute orders within agreed time windows.
• Operate and maintain peptide instrumentation.
• Independently run purification equipment.
• Lyophilization, aliquoting and pooling of peptides.
• Analyze peptide data using LC/MS and MW calculations.
• Perform ion-exchange on peptides in downstream production.
• GMP activities in cleanroom; support non-GMP as needed.
• Adhere to ISO 9001 quality system and GMP-API where applicable.
• Maintain compliance with company policies and procedures.

Skills

English (verbal/written)

Dutch language

Team player

Problem solving

Attention to detail

Multitasking

Can work under pressure

Hands-on mentality

Education

MBO/HBO in chemistry or related field

Tools

Office

SAP

Intrexx

Job description

Biosynth Netherlands is seeking a Laboratory Technician to support downstream peptide production in a cleanroom environment. You will perform purification, lyophilization and sample analysis, working closely with other peptide technicians to ensure timely delivery of materials.

Responsibilities include operating purification equipment, maintaining records, and complying with ISO 9001 and GMP-API where applicable. A hands-on, detail-oriented team player with lab experience is preferred.