Sterile Production Specialist
2 mesi fa
Job Summary: We are seeking a highly skilled Quality Specialist to join our team at Thermo Fisher Scientific. The successful candidate will play a key role in ensuring compliance with current US GMP, EU GMP regulations, and our company's outstanding quality standards.
Key Responsibilities:
- Assure constant monitoring of sterile production lines to ensure compliance with our company's quality standards.
- Implement thorough control measures to maintain outstanding quality throughout the production activities.
- Participate in defining and coordinating testing and validation activities for machinery, ensuring strict compliance with our company's quality standards.
- Collaborate with team members from different departments to settle quality standards and incorporate them into the production process.
- Analyze and resolve any problem or complaints to ensure that our products consistently meet the highest quality standards.
Requirements:
- A strong experience in the pharmaceutical environment.
- A scientific background and knowledge of machinery, equipment, and methodologies for pharmaceutical production, GMP regulations included.
- Familiarity with aseptic production challenges is a major plus.
- Confirmed experience in QA/Production in pharmaceutical companies is important, demonstrating the ability to efficiently implement quality control measures.
- Excellent communication skills, with the ability to build positive relationships and effectively connect with colleagues at all levels.
What We Offer:
- An outstanding opportunity to join a leading company in the pharmaceutical industry.
- A collaborative and dynamic work environment.
- The possibility to develop your skills and knowledge in a rapidly evolving industry.
Language: Italian and English.
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