Quality Assurance Engineer

We are seeking an experienced Pharmaceutical Validation Specialist to join our team in France.

This is a full-time position with a competitive salary, opportunities for professional growth, and a comprehensive benefits package. As a Pharmaceutical Validation Specialist at PharmEng Technology, you will be responsible for providing direct services to site Technical Services management, aiding to increase the throughput of commissioning and qualification activities through the department and across the site.

• Perform commissioning, qualification, requalification, and validation activities independently.
• Develop and implement quality systems and processes to ensure compliance with regulatory requirements.
• Conduct risk assessments and develop qualification documents such as VP, IQ, OQ, PQ, and PPQ protocols and reports.
• Support the development of user requirements and functional specifications.
• Evaluate projects and provide technical information to others.
• Recommend acceptance and release of qualified equipment/facilities/services/systems.

• Bachelor's degree in a technical field (engineering, biology, chemistry, pharmacy).
• At least 3 years of experience in QA Oversight for C&Q activities, in Biopharma or Pharma industry.
• Familiarity with cGMP validation requirements/guidelines and FDA regulatory requirements.
• Excellent communication and problem-solving skills.

The estimated salary for this position is €60,000-€80,000 per year, depending on experience.

• Full-Time Position
• Competitive Salary: €60,000-€80,000 per year
• Opportunities working for a global company
• Thirty (30) days Holiday
• Continuous Professional Improvement including courses or seminars

PharmEng Technology values diversity and inclusion. We are an equal opportunity employer and welcome applications from candidates with diverse backgrounds and experiences.