Senior Director, Site Quality Head, Goa

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   
* Assess and Mitigate Risks-- 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.
* Manage Quality Data--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
* Direct Quality Control-- 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
* Promote a Sustainable Culture of Quality---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.