Biotech and Agricultural Management & Business Others Medical and Healthcare Other Science and Tech
1 - 3 Years
January 11, 2019
Sr Supv Quality Function – 2545
Teva is a global pharmaceutical leader and the worlds largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
The supervisor QC-Innovative Laboratory Compliances combines appropriate line- management functionality with in-depth project management to meet all compliance related challenges. He/she is supported by an enthusiastic team capable of addressing issues in Pharmacopeial compliance, training compliance, Dossier compliance and equipment maintenance &qualification.
The SV is also responsible to plan various activities in close collaboration with the team as well as other stakeholders outside the site, while remaining aligned with strategy, commitments and goals of the organization.
1. Manage Quality& compliance
Manage the team in establishing and maintaining quality at the lab in accordance with Site SOPs, regulatory guidelines and cGXP compliance requirements.
Review and provide options to meet business needs without compromising quality and compliance.
Maintain a culture of enhancing quality throughout the entire Laboratory. Performance of in-depth root cause analyses
Act as SME during regulatory and internal audits.
Responsible for Method Life Cycle Management ensuring that analytical methods are up to standard, fit for purpose and in line with current regulations.
Responsible for maintaining the equipment qualification status according to regulatory and Teva standards
Responsible for maintaining compliance of QC analytical methods to Pharmacopeias and Regulatory filing
Planning , coordination of compliance projects
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 Compliance 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
Compliance should be your second nature
Good Knowledge with the use of Pharmacopoeia methods
Excellent organizational skills and a strong analytical oriented mindset.
Experience with working in a pharmaceutical environment
Experience with equivalence, method validation or method verification studies
Management Experience (2-3 yrs)
Affinity with equipment calibration&qualification
Good knowledge of Pharmaceutical quality systems and production processes
Good scientific analytical attitude
Excellent written and verbal communication skills
Pro-active team player
Quality Assurance Methods
Tevas Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.