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Senior Director, Site Quality Head, Goa

Teva Pharmaceuticals -
South Goa District, Goa

Apply Now

Job details

Benefits

Health insurance

Qualifications

Biology
Microbiology
Lean
Master's degree
Project management
Quality assurance
Bachelor's degree
Quality control
Chemistry
Quality systems
Manufacturing
Leadership
Lean manufacturing
FDA regulations

Full job description

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Senior Director, Site Quality Head, Goa

Date: May 14, 2026

Location: Goa, India, 403722

Company: Teva Pharmaceuticals

Job Id: 61480

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

The opportunity

Position responsibilities include Quality oversight for Manufacturing, Packaging and Laboratory Operations to ensure a mature culture of quality, compliance with regulatory requirements and quality of products.

This oversight includes but is not limited to the establishment and execution of procedure; Establishment Licensing, Quality on the Floor activities including audit and release; handling of laboratory, deviation and complaint investigations; CAPA Creation and implementation; trending and metrics, compliance with validation requirements; verification that equipment, facility and utility systems are maintained in accordance with established requirements.

Lead the development, standardization, implementation, monitor effectiveness and continuous improvement of Quality Systems, global and local compliance programs, industry practices, and corporate quality initiatives. Influence quality and compliance initiatives to implement robust and proactive process improvement programs within a strong quality culture to align and demonstrate compliance to Good Manufacturing Practices

Location

This role is based on the Teva site in Goa, India.

How you’ll spend your day

Leads the Quality organization on site including Quality Control, Microbiology, Quality Compliance, Quality Systems and Quality Assurance Operations.
Ensure a current Quality Management System is in place and continuously improved
Ensure products are manufactured, released and distributed in accordance to cGMP requirements and registered specifications.
Most senior professional and independent decision maker authority on product quality and potential market actions
- Identify quality risks and define proactive mitigations, to ensure the products are safe and effective before they reach the market. Work with the business to assure compliant and reliable supply
Design and Implement the Site Quality Program—Collaborate with the Site GM and Corporate Quality to create, implement, monitor and update the site quality program.
-Oversee the delivery of necessary data to site managers and supervisors, Corporate Quality and other internal and external stakeholders, to support the achievement of Quality objectives and ensure compliance
- Oversee the laboratory activity, including analytical site transfers, testing and approval or rejection of raw materials, packaging materials, in process materials and finished products for the site
-Create, develop and maintain a culture of enhancing quality throughout the entire site operation. Create a space where people can speak openly and are encouraged to present new ideas to improve quality
Maintain strong partnership with site leadership team
Strategic partner in the site leadership team, with Supply Chain, Project Management, R&D, MS&T and Commercial to ensure project timelines and objectives are met
Provide effective Quality leadership during internal, customer and Health Authority inspections
Ensure that Quality KPIs are meeting pre-defined targets, Ensures CAPA commitments are implemented in a timely manner and its effectiveness is monitored periodically
Plans, manages and monitors the annual Quality Operations budget and all its resources and employees. Ensure the performance and utilization of resources to provide maximum efficiency to the organization.

Your experience and qualifications

Required – bachelor’s degree in chemistry, Biology, Pharmacy
Preferred - Master or equivalent degree in Chemistry, Biology or Pharmacy

Key Requirements:

Minimum of 10 years pharmaceutical manufacturing site quality operations and leadership experience, including:
- Deep knowledge of cGMP requirements of local and major international authorities like EMA and US FDA for products and process,
- High level of understanding of manufacturing, packaging, technology transfer, cGMPs, EU, ICH guidelines as well as CMC content of regulatory submissions,
- Deep knowledge of chemical/pharmaceutical production operations/ lifecycle, production equipment/ validation and relevant technologies and product types,
- Strong understanding and experience in Data Integrity and Compliance
- Experience preparing and/ or leading regulatory authority GMP
- Deep knowledge of Quality Systems
Proven successful track record of leading organizational change to improve efficiency
Experience leading, inspiring and coaching large teams
Experience developing and implementing and continuously improve existing and new, efficient, and effective business processes
Must have adequate knowledge of Quality best practices
Must have adequate practical knowledge of pharmaceuticals manufacturing and/ or control
Must have adequate practical knowledge of analytical techniques and microbiological principles
Must have practical knowledge of pharmaceutical cross functional operations (e.g., Supply Chain, Engineering), product and tech transfer
Must have practical knowledge on lean manufacturing/ lean QC and OPEX tools
Good knowledge of environmental, health and safety requirements for laboratories and quality operations.

How We’ll Take Care of You

At Teva India, care is at the heart of how we work. From your first day, you’ll be welcomed into a people-first culture built on inclusion, respect, and belonging.
That support extends to you and your loved ones through benefits designed for real life. These include comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, and confidential emotional wellbeing support through our Optum Employee Assistance Program. You’ll also enjoy healthy meals at work, holistic wellbeing initiatives, and volunteering programs that help you give back to the community.

Your growth matters too. You’ll have opportunities to build future-ready skills, collaborate on projects with global teams, explore internal career opportunities, and learn through programs such as our AI-enabled Teva Twist program, R&D Academy, continuing education, and mentorship.

Join our vibrant workplace, where we celebrate milestones, festivals, achievements, and community impact together.

Teva’s 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, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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