We are looking for a proactive and independent Lab Responsible to support Quality Control (QC) and Process Development activities within an innovative biotechnology environment.
In this role, you will combine quality oversight, documentation management and practical laboratory support. You will play an important role in ensuring compliance, maintaining accurate records and supporting efficient laboratory operations.
What's offered?
Ready to grow your career and make real impact? Join MindCapture!
- competitive salaries
- meal vouchers
- eco vouchers
- DKV health insurance
- group insurance
- net expense allowance
- company car
- personalised training and development
At MindCapture, you choose what you love, build on your strengths, and make a difference where it matters most.
You will work as a MindCapture consultant for an international start up in the biotechnology industry.
Job Description:
- Maintain and update laboratory procedures within the document management system.
- Monitor stock levels of chemicals, laboratory materials and consumables.
- Follow up on preventive maintenance and calibration activities for laboratory equipment, including balances, incubators and pipettes.
- Perform internal maintenance and calibration checks when required, ensuring accurate documentation.
- Prepare culture media and basic laboratory solutions while maintaining complete preparation records.
- Review development records and associated study documentation for accuracy and completeness.
- Perform incoming goods inspections for the GMP Quality Control laboratory and register ordered materials.
- Support quality compliance and documentation processes across Quality Control and Process Development activities.
- Collaborate closely with laboratory colleagues and management to ensure efficient daily operations.
Requirements:
- Bachelor’s degree in Biochemistry, Biotechnology or a related scientific discipline.
- At least 2 years of relevant laboratory experience.
- Basic knowledge of laboratory operations, procedures and equipment.
- Strong attention to detail with a critical mindset towards documentation review and quality compliance.
- Accurate and precise approach to laboratory activities and administrative tasks.
- Proactive attitude with the ability to work independently and take ownership of responsibilities.
- Strong organisational skills and flexibility to manage activities across different departments.
- Experience working within a quality management system, particularly cGMP, is an advantage.
- Fluency in Dutch and English, both written and spoken.
Are you ready to make a real difference in healthcare?
Join our dynamic team and help drive innovation in medical devices.