
Will you join us as a
Quality Assurance Manager?
About Green Elephant
Green Elephant Biotech is a rapidly growing startup at the forefront of innovation in the biotechnology sector. Our technology is redefining adherent cell culture by significantly enhancing efficiency and scalability in biopharmaceutical manufacturing, from research to the production of cutting-edge cell and gene therapies.
Join us and be part of a team dedicated to transforming biotechnology through innovation and sustainability.
What we're looking for
We are seeking a Quality Management Specialist (m/f/d) to ensure and further develop our high standards of quality and compliance. In this role, you will maintain and enhance our electronic quality management system in line with ISO 9001 and cGMP standards, support internal and external audits, and drive continuous improvement initiatives. You’ll collaborate closely with various departments to ensure seamless processes and compliance across the organization. This is a fantastic opportunity to contribute to a dynamic and growing company in the biopharmaceutical industry.
Why join us
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Attractive total compensation package.
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Flexible working hours and the opportunity to work part-time from home.
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Fast decision-making processes in a dynamic, innovative environment.
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Opportunity for professional growth within a rapidly expanding company.
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Contribute to a company making a meaningful impact on sustainability in the biotech industry and accessibility of cell and gene therapies.
Key responsibilities
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Maintenance, improvement, and further development of the existing electronic quality management system in accordance with ISO 9001 and cGMP standards
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Support in conducting internal and external audits
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Analysis of quality data and derivation of corrective and preventive actions with a focus on continuous improvement
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Maintenance and assurance of the supply chain
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Validation of computer-based systems
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Ensuring compliance with quality standards and guidelines
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Close collaboration with other departments
Who you are
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A degree in natural sciences, ideally with initial professional experience in quality management, quality assurance, production, or quality control in the pharmaceutical industry, or in quality assurance at an ISO 9001-certified production facility
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Solid knowledge of quality management systems (e.g., ISO 9001, cGMP)
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Proficiency in Microsoft Office applications
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Excellent English language skills
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Strong communication skills and a confident, professional demeanor
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A structured and detail-oriented approach to work
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Quick comprehension, strong sense of responsibility, and excellent decision-making abilities
