Assoc Dir Quality Control

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.

How You’ll Spend Your Day

1.    Quality Control Laboratory

Handling all the Quality Control Laboratory operations in compliance with Good Laboratory Practices and Safety policies.

Selection, upgradation, procurement, installation and qualification of laboratory instruments and equipment.

Preparing and monitoring of Capex and Revenue budget for laboratory.

Preparation and execution of cost improvement plans for the laboratory expenses.

To identify the needs and to provide resources, adequate facility required for effective and efficient functioning of the department for timely analysis of samples.

2.    Quality Management

Oversees the implementation of Standard Operating Procedures relating to the laboratory activities and compliance with the requirements of Good Laboratory practices.

Upgradation of laboratory systems as per the regulatory requirements.

Oversees calibration and preventive maintenance of laboratory instruments and equipment as per schedule, in accordance with approved Standard Operating Procedures. To arrange vendor assistance for AMC and other Instrument/ equipment breakdown.

To ensure upkeep and maintenance of all laboratory standards as per written procedures and to arrange the Laboratory standards based on forecast and priorities.

Responsible for monitoring the activities pertaining to upkeep and maintenance of Narcotics and controlled substances.

3.    Stability Study

To ensure identification, tracking and Co-ordination of all stability batches packed at Goa site and at other approved packing site.

Responsible for activities related to stability management.

To ensure planning, supervision and review activities of Commercial Stability Study Samples, Hold Time study Sample, Temperature Excursion, and Thermal Cycling.

4.    Documentation

Responsible for review of Specifications, Test Methods, Analytical Worksheet, Analytical Method Transfer/Verification/validation Protocol and Reports and Standard Operating Procedure of the Quality Control department.

Ensures review and approval of departmental and site documents.

5.    Budget and Inventory Management

Ensure timely submission and monitoring of QC laboratory Capex budget.

Initiation of Capital Expenditure Request as per agreed Quarter to match cash flow and procurement of budgeted items.

Ensure completion of Unbudgeted Capital Expenditure Request as per requirement.

Capex assets and inventory management in co-ordination with Finance department.

6.    Inspections/Audits

Participates in the self-inspection program conducted by the Quality Assurance Department.

Ensures Audit readiness of Quality Control Laboratory and to face all regulatory and customer inspections and ensure compliance.

Active participation in regulatory Audits, customer audits and compliance.

7.    Data Integrity

To ensure compliance to the requirements of policy and procedures on Data Integrity.

To ensure that the GxP data handling is secure and adopt measures to ensure data Integrity.

To make sure that the current systems and practices are challenged to guarantee that data integrity is maintained.

8.    Operational Excellence

Preparation and execution of cost improvement plans in co-ordination with OpEx team to reduce laboratory expenses.

OpEx initiatives in the laboratory such as Implementation of 5S standards for laboratory consumables, chemicals and instrument spares for easy traceability and to reduce searching time, Process simplification and efficiency enhancement.

Identification and execution of efficiency enhancement projects

Your Skills and Experience

Bachelor or Master of Science / Pharmacy

15 – 20 years of experience in the Pharmaceutical Industry handling QC 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.

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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.