Teva Pharmaceutical USA

Sr Dir, Site Quality Head, Goa and Asia Cluster

Teva Pharmaceutical USA

Goa 403722, India
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Welcome to Teva Pharmaceutical USA – a leading global pharmaceutical company dedicated to improving the lives of patients around the world. We are currently seeking a highly skilled and experienced Senior Director to join our team as the Site Quality Head for our Goa and Asia Cluster. In this role, you will have the exciting opportunity to lead and manage all quality operations for our manufacturing site in Goa, India, as well as our Asia Cluster, ensuring adherence to global quality standards and regulations. We are looking for a dynamic and driven individual with a strong background in quality control, compliance, and leadership. If you are passionate about making a meaningful impact in the pharmaceutical industry and have the necessary qualifications, we invite you to apply for this key position at Teva Pharmaceutical.

  1. Oversee and manage all quality operations for the manufacturing site in Goa and the Asia Cluster, ensuring compliance with global quality standards and regulations.
  2. Develop and implement quality policies and procedures to ensure product safety, efficacy, and compliance with regulatory requirements.
  3. Lead a team of quality professionals, providing guidance, training, and support to ensure a high level of performance and adherence to quality standards.
  4. Collaborate with cross-functional teams, including production, supply chain, and regulatory affairs, to ensure timely and efficient execution of quality activities.
  5. Monitor and report on quality metrics to senior management, identifying areas for improvement and implementing corrective actions as needed.
  6. Stay updated on industry trends, changes in regulations, and best practices to continuously improve quality operations and maintain compliance.
  7. Conduct audits and inspections of the manufacturing site and suppliers to ensure compliance with quality standards and regulations.
  8. Manage relationships with regulatory authorities and act as the primary point of contact for quality-related inquiries and inspections.
  9. Drive a culture of quality and continuous improvement throughout the organization, promoting a proactive and preventative approach to quality management.
  10. Represent Teva Pharmaceutical at industry conferences and events, demonstrating our commitment to quality and safety in pharmaceutical manufacturing.
Where is this job?
This job is located at Goa 403722, India
Job Qualifications
  • Extensive Experience In Quality Assurance: The Ideal Candidate Should Have At Least 10 Years Of Experience In Quality Assurance, With A Strong Understanding Of Pharmaceutical Quality Systems And Regulatory Requirements.

  • Leadership And Team Management Skills: As A Senior Director, The Candidate Should Have Proven Experience In Leading And Managing A Team, With The Ability To Mentor And Develop Team Members To Achieve Quality Objectives.

  • Knowledge Of Global Quality Standards: The Candidate Should Possess A Thorough Understanding Of Global Quality Standards, Including Fda Regulations, Ich Guidelines, And Other Relevant Regulatory Requirements For The Pharmaceutical Industry.

  • Quality Control And Compliance Expertise: The Candidate Should Have A Track Record Of Success In Implementing Effective Quality Control And Compliance Strategies, With Experience In Conducting Gmp Audits And Inspections.

  • Strong Communication And Interpersonal Skills: As A Senior Leader, The Candidate Should Have Excellent Communication And Interpersonal Skills, With The Ability To Effectively Collaborate With Cross-Functional Teams And Communicate Quality Objectives And Results To Senior Management.

Required Skills
  • Risk Management

  • Quality Assurance

  • Process Improvement

  • Data Analysis

  • Team Management

  • GMP

  • Leadership

  • Auditing

  • Regulatory compliance

  • Training and Development

  • Problem-Solving

  • ROOT

Soft Skills
  • Communication

  • Conflict Resolution

  • Emotional Intelligence

  • Leadership

  • Time management

  • creativity

  • Organization

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Sr Dir, Site Quality Head, Goa and Asia Cluster in Goa 403722, India is approximately Rs. 20-25 lakhs per annum. This salary range can vary based on factors such as experience, industry, and company size.

Additional Information
Teva Pharmaceutical USA is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesHindi
Job PostedApril 18th, 2025
Apply BeforeJuly 20th, 2025
This job posting is from a verified source. 

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About Teva Pharmaceutical USA

Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S. Teva Pharmaceutical Industries Ltd. engages in the provision of pharmaceutical services. It operates through the following business divisions: Generic, Specialty Medicine, and Over-the-Counter (OTC).

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