Quality Control Technician

About the role

Responsible for planning/coordinating testing and inspection activities related to company products, and recording, analyzing and approving results during product development and manufacturing. Also responsible for environmental monitoring activities.

Responsibilities

• Cordination and planning of internal and external QC testing
• Performance and reporting of inspection and testing of raw materials, production related materials and company products (intermediate and finished products)
• Sampling of (raw) materials and products for inspection & testing
• Release of raw materials and production related materials
• Cordination, planning, performance and reporting of environmental monitoring (EM) of production areas and utilities
• Cordination, planning and testing of samples relating to shelf life and validation studies
• Calibration and maintenance of QC and EM related equipment, and maintenance of QC laboratory/areas

Key Responsibilities

• Technical
• QA/QC Regulatory
• Safety/Organizational/Productivity

Qualifications

• Bachelor Biomedical, Biotechnology, Laboratory
• Experience with relevant Quality systems and regulatory requirements ISO 13485 / ISO 9001 / cGMP (FDA 21CFR820- QSR)
• Technical experience relating to testing of medical devices.
• English language on C-Level

Skills

• Able to work independently, hands on mentality.
• Accurate and pro-active.
• Good interpersonal and communication skills are necessary.
• Team player, able to work cooperatively in a professional team.

Physical Requirements and Work Conditions

• Mobility & Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping.
• Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role.
• Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment.
• Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver’s license.

Kuros Biosciences

Kuros is a Swiss-headquartered biotech company, listed on the SIX Swiss Stock Exchange since 2016 (under symbol KURN). With additional operations in the Netherlands and the USA, we continue to grow our global team.

To deliver the ideal bone graft, you need the highest quality and quantity of scientific evidence behind it. We believe that this is a key differentiator for Kuros, given the urgent need to advance bone healing.

• Listed on the SIX Swiss Exchange under the symbol KURN since 2016
• A commercial & research footprint that spans >20 markets
• Dozens of clinical and scientific expert Advisers
• Over 25 orthobiologics-related patents
• Over 400 patients evaluated in Level I, randomized controlled clinical trials
• Over 20 well-controlled Level I-IV clinical trials initiated, including 6 that are complete1
• Published Level I evidence published in Spine

Our credentials

Kuros Biosciences is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.

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