1. Manage Stability & Investigation

• Guide team in Stability & investigation strategies
• Guide team in implementation of Pharmaceutical and Dossier compliance tasks
• Manage the team in establishing and maintaining quality at the lab in accordance with Site SOP’s, regulatory guidelines and cGXP compliance requirements.
• Maintain a culture of enhancing quality throughout the entire Laboratory. Performance of in-depth root cause analyses and problem solving
• Act as SME during regulatory and internal audits.
• Responsible for intercompany communication with external TEVA Global Analytical Stability Laboratory
• Responsible for adherence to planning and execution of stability programs for commercial drug products.

2. Manage Team and Resources

• Manage own team through talent identification, active performance management, succession planning, employee development, mentoring and modeling behavior according to Teva values.
• Run an efficient and effective QC Stability& Investigation team through managing the team budget and resources.

3. Manage of Culture of Safety

• Maintain a culture of enhancing safety throughout the entire Laboratory.
• Review and provide options to meet business needs without compromising health & safety.

Qualifications

Function

Sub Function

Reports To

Head of QC Analytical Laboratory

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