Teva Pharmaceuticals is looking for an experienced professional for the position of Quality Control Technician III at its Goa, India facility. This opportunity is part of the company’s Nitrosamine team at the Watson Pharma Pvt. Ltd. Goa Facility and is focused on analytical testing, method development and validation activities related to nitrosamine impurities.
The position is suitable for candidates with a background in M.Sc. Chemistry or M.Pharm and 3–5 years of hands-on experience in analytical method development and validation. Candidates should have knowledge of analytical chemistry, pharmaceutical quality systems, ICH guidelines and regulatory-compliant laboratory practices.
The role also involves working with advanced analytical techniques and instruments such as LCMS, GCMS and IC, along with laboratory documentation, data integrity, instrument maintenance and compliance activities.
Teva Recruitment 2026 – Job Highlights
| Job Details | Information |
|---|---|
| Company | Teva Pharmaceuticals |
| Facility | Watson Pharma Pvt. Ltd. Goa Facility |
| Job Position | Quality Control Technician III |
| Department/Team | Quality Control / Nitrosamine |
| Location | Goa, India |
| Qualification | M.Sc. Chemistry or M.Pharm |
| Experience | 3–5 Years |
| Core Area | Analytical Method Development & Validation |
| Key Focus | Nitrosamine Impurity Testing |
| Employment Type | Not specified in provided information |
| Salary / CTC | Not disclosed |
| Application Mode | Official Teva Careers Portal |
About Teva Pharmaceuticals
Teva is a global biopharmaceutical company with a major generics business and operations focused on delivering medicines to patients worldwide.
The Goa opportunity is associated with the company’s Nitrosamine team, which works on activities important to pharmaceutical product quality, patient safety and regulatory compliance.
The role provides an opportunity for an analytical science professional to work on laboratory activities involving nitrosamine-related testing and analytical method development.
Job Description
Quality Control Technician III
The Quality Control Technician III will support analytical activities related to nitrosamine impurities at Teva’s Goa facility.
The position includes developing and validating analytical methods under the guidance of senior team members, testing samples, managing laboratory materials and maintaining compliance with applicable quality and regulatory requirements.
The professional will also be involved in analytical documentation, instrument operation, troubleshooting, calibration and laboratory data integrity.
Eligibility Criteria
Educational Qualification
Candidates should have either:
- M.Sc. in Chemistry, or
- M.Pharm
Experience
Applicants should have:
- 3–5 years of hands-on experience in analytical method development and validation.
- Relevant knowledge of analytical chemistry.
- Experience working in pharmaceutical laboratory environments.
- Understanding of cGMP/GLP practices and regulatory documentation.
Technical Knowledge and Skills
Candidates should have strong knowledge of:
- Analytical Chemistry
- Analytical Method Development
- Analytical Method Validation
- Nitrosamine impurity analysis
- Drug Substance testing
- Drug Product testing
- Pharmaceutical Quality Systems
- ICH Guidelines
- cGMP
- GLP
- Regulatory-compliant documentation
- Laboratory data integrity
- Analytical instrument operation
Experience with LCMS, GCMS and IC related activities is relevant to the role.
Key Responsibilities
The selected professional may be responsible for the following activities:
Analytical Method Development and Validation
- Develop and validate analytical methods for nitrosamine-related activities.
- Work with analytical techniques including LCMS, GCMS and IC under senior team guidance.
- Conduct literature searches to support analytical method development.
- Apply a logical and scientific approach to analytical problem-solving.
Sample Management and Testing
- Manage samples received from different sites for nitrosamine projects.
- Perform testing of samples associated with nitrosamine-related activities.
- Maintain accurate records associated with sample handling and testing.
- Support laboratory activities while maintaining data quality and integrity.
Instrument Operation and Troubleshooting
- Operate laboratory analytical instruments as required.
- Perform routine calibration and maintenance activities.
- Troubleshoot day-to-day instrument-related issues.
- Escalate technical problems when additional support is required.
- Maintain accurate instrument usage and calibration records.
Laboratory Materials and Documentation
- Monitor and maintain laboratory prerequisites such as:
- Columns
- Analytical standards
- Chemicals
- Spare parts
- Consumables
- Prepare analytical protocols and reports.
- Maintain technical documentation in accordance with regulatory requirements.
Quality and Compliance
- Follow applicable cGMP and GLP requirements.
- Maintain laboratory compliance and data integrity.
- Follow pharmaceutical quality system requirements.
- Work according to applicable ICH guidelines.
- Follow EHS requirements and safe laboratory practices.
- Participate in internal audits.
- Support laboratory readiness for external inspections.
Computerized Systems
The vacancy mentions familiarity with computerized systems such as:
- TrackWise
- Veeva Vault
Knowledge of these systems can support documentation, quality and compliance-related activities.
Additional Preferred Skill
Hands-on experience with Mass Hunter Software is an additional advantage for this position.
Key Skills for Quality Control Jobs
- Analytical Chemistry
- Analytical Method Development
- Analytical Method Validation
- Nitrosamine Impurity Analysis
- LCMS
- GCMS
- IC
- Pharmaceutical Quality Systems
- cGMP
- GLP
- ICH Guidelines
- Laboratory Data Integrity
- TrackWise
- Veeva Vault
- Mass Hunter
- Instrument Troubleshooting
- Technical Documentation
- Laboratory Compliance
Work Location
The position is associated with the Watson Pharma Pvt. Ltd. Goa Facility in Goa, India.
The provided vacancy information does not specify shift timings, remote-work arrangements or exact working hours.
Salary / CTC
The salary or CTC for the Quality Control Technician III position has not been disclosed in the provided vacancy information.
Candidates should confirm compensation and other employment terms directly through Teva’s recruitment process.
Employee Benefits and Career Development
Teva states that employees may have access to benefits and programs that support wellbeing and career development. These include annual leave, reward plans, flexible working arrangements where applicable, health support and professional development opportunities.
The company also highlights its Twist career development platform, which provides access to learning programs, short-term projects and internal career development opportunities.
The availability and terms of individual benefits may vary depending on the applicable role, location and employment conditions.
Selection Process
The detailed selection process has not been specified in the provided vacancy information.
Candidates whose qualifications and experience match the requirements may be contacted by Teva for further stages of the recruitment process.
How to Apply
Interested and eligible candidates should apply through the official Teva Careers Portal and search for the Quality Control Technician III position associated with the Goa facility.
Candidates should ensure that their application clearly highlights:
- M.Sc. Chemistry or M.Pharm qualification
- 3–5 years of analytical method development and validation experience
- Nitrosamine impurity analysis experience
- LCMS, GCMS or IC experience
- cGMP/GLP knowledge
- ICH guideline knowledge
- TrackWise/Veeva Vault exposure
- Laboratory documentation and data integrity experience
- Mass Hunter experience, if applicable
Important Details Before Applying
- Company: Teva Pharmaceuticals
- Position: Quality Control Technician III
- Location: Goa, India
- Facility: Watson Pharma Pvt. Ltd.
- Team: Nitrosamine
- Qualification: M.Sc. Chemistry or M.Pharm
- Experience: 3–5 years
- Core Expertise: Analytical Method Development & Validation
- Key Techniques: LCMS, GCMS, IC
- Systems: TrackWise, Veeva Vault
- Additional Advantage: Mass Hunter Software
- Salary: Not disclosed
- Application: Teva Careers Portal
Frequently Asked Questions
1. What position is Teva hiring for in Goa?
Teva is hiring for the position of Quality Control Technician III.
2. Where is the position located?
The role is based at the Watson Pharma Pvt. Ltd. Goa Facility in Goa, India.
3. What qualification is required?
Candidates should have an M.Sc. in Chemistry or M.Pharm.
4. How much experience is required?
The vacancy requires 3–5 years of hands-on experience in analytical method development and validation.
5. Is nitrosamine experience relevant to this role?
Yes. The position is part of the Nitrosamine team and involves analytical method development, validation and testing related to nitrosamine impurities.
6. Which analytical techniques are mentioned?
The job description specifically mentions LCMS, GCMS and IC for nitrosamine-related analytical activities.
7. Is Mass Hunter experience required?
Mass Hunter Software experience is listed as an additional desirable skill, rather than a mandatory qualification.
8. Which computerized systems are mentioned?
The vacancy mentions familiarity with TrackWise and Veeva Vault.
9. Is salary mentioned for this Teva vacancy?
No. The salary or CTC has not been disclosed in the provided job information.
Important Note
Job availability, eligibility requirements, salary, benefits, application status and other employment conditions may be updated by Teva. Candidates should verify the latest vacancy details through the official Teva Careers Portal before applying. Meeting the stated eligibility criteria does not guarantee selection.