Thermo Fisher Scientific
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
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.
Senior Manager, Compliance
Job not on LinkedIn
🕒 June 20
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
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.
📋 Description
• Conduct internal audits of Thermo Fisher Pharma Services Group (PSG) manufacturing and Clinical Trial Division (CTD) sites • Prepare detailed audit reports to communicate observations • Maintain knowledge of GMPs and emerging quality regulations • Promote positive Quality and leadership behaviors • 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 • Must be an expert Quality compliance auditor • Experience in sterile manufacturing and aseptic practice is desired • Professional auditor training/certification by an organization recognized within the pharmaceutical industry (e.g. IRCA, ASQ) • Bachelor’s Degree in Pharmacy, Science or Engineering • Strong foundation of pharmaceutical manufacturing and laboratory operations • Strong communication skills including listening, judgment, problem management
🏖️ Benefits
• Health insurance • Professional development opportunities
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