Teva Walkin Quality Control & Quality Assurance professionals
- Company Overview
- Job Role & Responsibilities
- Quality Control – Analytical
- Quality Assurance – Compliance
- Eligibility / Qualifications
- Educational Requirements
- Experience Requirements
- Preferred Technical Exposure
- Location & Salary
- Walk-In Interview Details
- Application Process
- Frequently Asked Questions
- Who can attend this walk-in interview?
- Is formulation experience required?
- What instruments should candidates be familiar with?
- Is this a permanent role?
- Is Teva a certified workplace?
- Summary Table
Teva hiring Quality Control & Quality Assurance professionals in Chennai. M.Sc Chemistry with 1–10 years pharma experience eligible.
Teva is conducting a walk-in interview drive for Quality Control and Quality Assurance professionals at its Chennai development center. This opportunity is ideal for experienced M.Sc Chemistry professionals from pharmaceutical formulation backgrounds who want to work in a globally recognized, Great Place to Work–certified organization. The roles offer hands-on exposure to advanced analytical instruments, stability studies, method transfers, and quality systems across multiple dosage forms.
Company Overview
Teva is one of the world’s leading pharmaceutical companies, committed to making quality medicines accessible and affordable. With a strong global footprint, Teva operates across generics, specialty medicines, and complex dosage forms, supported by robust R&D and quality systems.
Teva Actavis Pharma Development Centre Pvt. Ltd., located at TICEL Bio Park, Chennai, plays a key role in formulation development, analytical testing, and quality assurance for regulated markets. The organization is known for its compliance-driven culture, strong ethical standards, and continuous investment in people and technology.
Job Role & Responsibilities
Teva is hiring experienced professionals for both Quality Control and Quality Assurance functions. Selected candidates will support analytical testing, quality compliance, and validation activities across diverse pharmaceutical dosage forms.
Quality Control – Analytical
Key Responsibilities
- Operate and maintain analytical instruments including HPLC, UPLC, LCMS, GCMS, GC, UV, IR, and Dissolution systems
- Perform analysis of raw materials, in-process samples, finished products, and stability samples
- Execute and support stability studies as per regulatory guidelines
- Perform method transfer and method validation activities
- Support nitrosamine testing and impurity profiling as applicable
- Ensure data integrity, documentation accuracy, and compliance with SOPs
Quality Assurance – Compliance
Key Responsibilities
- Support quality systems and GMP compliance activities
- Review analytical data, stability reports, and validation documentation
- Ensure adherence to regulatory and internal quality standards
- Participate in investigations, deviations, and CAPA activities
- Support audits and inspection readiness
Eligibility / Qualifications
Educational Requirements
- M.Sc Chemistry
Relevant Courses (comma-separated): M.Sc Chemistry, Analytical Chemistry, Pharmaceutical Chemistry
Experience Requirements
- Quality Control: 2–10 years of experience in pharmaceutical companies
- Quality Assurance: 1–3 years of experience in pharmaceutical quality roles
Preferred Technical Exposure
- Hands-on experience with stability studies, method transfer, and validations
- Experience across dosage forms such as OSD, ointments, creams, suppositories, lotions, syrups, gels, drops, ampoule injectables, FOS, and oral liquids
- Exposure to nitrosamine testing is an added advantage
Location & Salary
- Walk-In Location: Teva Actavis Pharma Development Centre Pvt. Ltd.
- Address: TICEL Bio Park, Phase 1, Ground Floor, Taramani Road, Taramani, Chennai, Tamil Nadu – 600113
- Employment Type: Full-time
- Salary: Best in industry and commensurate with experience
Walk-In Interview Details
- Date: Saturday, 24 January 2026
- Time: 10:00 AM to 3:00 PM
- Venue: TICEL Bio Park, Taramani, Chennai
Candidates are advised to carry updated resumes and relevant documents.
Application Process
This is a direct walk-in interview. Interested candidates should attend the interview in person at the given venue and time.
Frequently Asked Questions
Who can attend this walk-in interview?
M.Sc Chemistry professionals with relevant pharmaceutical QC or QA experience can attend.
Is formulation experience required?
Yes. Candidates with pharmaceutical formulation experience are preferred.
What instruments should candidates be familiar with?
HPLC, UPLC, LCMS, GCMS, Dissolution, UV, and IR are preferred.
Is this a permanent role?
Yes. These are full-time roles.
Is Teva a certified workplace?
Yes. Teva is Great Place to Work–certified.
Summary Table
| Company | Teva |
|---|---|
| Vacancies | Quality Control, Quality Assurance |
| Required Education | M.Sc Chemistry |
| Experience | 1–10 Years |
