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Sr. Manager, Microbiology Quality Compliance Expert 1
Date: Jun 27, 2025
Location:Santhia, Italy, 00
Company: Teva Pharmaceuticals
Job Id: 62539

WHO WE ARE

TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With
the industry’s broadest portfolio including over 350 API products, TAPI is the go-to global
supplier for APIs, supporting 75% of the top 50 global pharmaceutical companies.
Headquartered in Israel, TAPI employs more than 4,000 professionals at 13 sites worldwide.
We provide superior product quality and excellent customer service.

THE OPPORTUNITY

We are looking for a Sr Manager, Microbiology-Quality Compliance Expert - TAPI.
The main purpose of your job will be to ensure that the Microbiology laboratories, systems , procedures related to Quality Compliance System at TAPI sites is in place, securing compliance of activities, OOS investigations, Micro CCS, quality risk management, escalation of risks, and continuous improvement. Your role will include providing governance through strong collaboration with manufacturing site operations to foster excellence in inspection management and inspection readiness at TAPI sites. You will support manufacturing site remediation activities directly.
This role will ensure that each site receives the right level of support to sustain and continuously improve GMP compliance related to Microbiology and other quality compliance support, to strategize the development and overall implementation of remedial plans, to solve quality-related compliance issues, to identify areas of improvement for quality operational performance in line with business needs and in accordance with TAPI standards. Moreover, you will foster and develop onsite Quality culture across all sites.

YOUR EXPERIENCE AND QUALIFICATIONS

• Degree in Industrial Microbiology and demonstrated knowledge in cGXP regulations.
• 10+ years’ experience in GMP environment, continuous professional development 5+ years’ experience in Microbiology laboratory, managerial tasks, organization Exposure to International working environment
• Mix of experience in Micro, Quality systems would be preferred.
• Very good understanding and insight into the different aspects of quality functions like QC, QA, Quality Systems, Compliance, etc.
• Sound knowledge of regulatory standards and guidance in Pharmaceutical Industry and expectation of global regulatory bodies, including US FDA, PMDA and ANVISA requirements
• Performance management and reporting
• Project management, monitoring, execution and reporting
• Problem solving and good team work skills
• Proactive orientation, communication skills
• Proven influencing capabilities
• Fluent in English

• Establish and monitor governance on data integrity requirements.
• Cooperate with other functions on Quality projects and their role out.
• Act as a quality SME and support global compliance initiatives upon request
• Participate in audits upon request.
• Fosters knowledge sharing among sites within the TAP