Thermo Fisher Scientific
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Senior Compliance Manager
Job not on LinkedIn
October 3
Thermo Fisher Scientific
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
📋 Description
• Conduct internal audits of Thermo Fisher Pharma Services Group manufacturing and Clinical Trial Division sites • Prepare detailed audit reports to communicate observations • Maintain knowledge of GMPs and revised or emerging quality regulations • Participate in ad-hoc quality compliance projects related to auditing
🎯 Requirements
• Minimum of 10 years professional working experience in Pharmaceutical Industry • At least 5 years aggregate experience performing audits for GMP, ISO or ICH • Hosting/supporting FDA, EMA, MHRA, AIFA, ANVISA inspections • Must be an expert Quality compliance auditor • Experience with elements of data integrity in a pharmaceutical manufacturing environment • Strong foundation of pharmaceutical manufacturing and laboratory operations • Professional auditor training/certification by an organization recognized within the pharmaceutical industry • Bachelor's Degree in Pharmacy, Science or Engineering
🏖️ Benefits
• Standard (Mon-Fri) • Adherence to all Good Manufacturing Practices (GMP) Safety Standards
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