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QA Specialist
ProGnosis Biotech S.A., a fast-growing and innovative biotechnology company, is looking for a QA Specialist to join its team in Larissa.
We are seeking a professional with experience in Quality Assurance, good knowledge of quality systems and regulatory requirements, and the ability to collaborate effectively with different departments. The ideal candidate will contribute to the proper implementation, monitoring and continuous improvement of the company’s quality processes.
The Role
As a QA Specialist, you will support Quality Assurance activities, monitor compliance with quality standards and internal procedures, and ensure the proper maintenance of quality documentation.
The role requires strong organizational skills, attention to detail, analytical thinking and close collaboration with Production, R&D, Regulatory and Quality Control departments.
Key Responsibilities
- Support the planning, implementation and monitoring of Quality Assurance activities.
- Monitor compliance with regulatory requirements, quality standards and internal procedures.
- Ensure that the company’s products, processes and records meet defined quality standards.
- Prepare, review and manage quality documentation, SOPs, protocols and reports.
- Support the preparation, organization and follow-up of internal and external audits.
- Monitor deviations, CAPAs, change control and related follow-up actions.
- Maintain and review records in accordance with ISO and QMS requirements.
- Collaborate with Production, R&D, Regulatory and Quality Control departments to resolve quality and compliance-related issues.
Requirements
- Bachelor’s degree in Chemistry, Biology, Biotechnology, Pharmacy, Biomedical Sciences, Food Science or a related field.
- Minimum of 3 years of experience in a Quality Assurance role, preferably within the pharmaceutical, biotechnology, medical device or other regulated industry.
- Good knowledge of regulatory requirements, quality management systems and compliance procedures.
- Experience in preparing, reviewing and managing quality documentation.
- Familiarity with ISO 13485, ISO 9001 or other relevant quality standards.
- Excellent command of English, both written and verbal.
- Good command of Greek, both written and verbal.
- Strong organizational skills and attention to detail.
Nice to Have
- Experience or familiarity with IVDR – Regulation (EU) 2017/746.
- Experience with medical devices or IVD products.
- Knowledge of technical documentation, risk management and validation processes.
- Experience in internal and/or external audits.
- Experience in biotechnology, diagnostics or a related regulated environment.
Personal Skills and Competencies
We are looking for a professional with:
- Analytical thinking and strong problem-solving skills.
- Strong organizational, planning and multitasking abilities.
- Responsibility, consistency and professionalism.
- Team spirit and good communication skills.
- Ability to work both independently and collaboratively with different departments.
- Strong attention to detail and focus on compliance and quality.
What We Offer
- Competitive salary, commensurate with experience and qualifications.
- A dynamic and collaborative work environment.
- Opportunities for professional development and career growth.
- Involvement in innovative products within the biotechnology sector.
- An active role in maintaining and improving the company’s quality systems.
- Collaboration with specialized teams and different departments across the company.
How to Apply
To apply, please send your resume and cover letter to humanresources@prognosis-biotech.com with the subject ”QA Specialist – Larissa”.
All applications will be treated with strict confidentiality. We look forward to receiving your application!
Job Type: Full-time
Location: Larissa, Greece
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