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.
Bachelor or Master degree in analytical chemistry/pharmacy or equivalent experience
Good Knowledge with the use of ICH guidelines and Pharmacopoeia methods
Excellent organizational skills and a strong analytical oriented mindset.
Experience with working in a pharmaceutical environment
Solid experience with equivalence, method validation or method verification studies
Management Experience is preferred (2-3 yrs)
Good knowledge of Pharmaceutical quality systems and production processes
Good scientific analytical attitude
Excellent written and verbal communication skills
Pro-active team player
Head of QC Analytical Laboratory
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