Teva Pharmaceuticals has announced an opportunity for the position of Quality Control Analyst I in Chennai, Tamil Nadu. The role is suitable for experienced professionals with an M.Sc. in Biochemistry and substantial experience in pharmaceutical quality control and analytical activities.
The position involves stability analysis, analytical method transfer, method validation, instrument calibration, quality documentation, LIMS, TrackWise, and EDMS activities.
Teva Quality Control Analyst I Recruitment 2026 – Overview
| Particulars | Details |
|---|---|
| Company Name | Teva Pharmaceuticals |
| Job Role | Quality Control Analyst I |
| Job ID | 69148 |
| Job Location | Chennai, Tamil Nadu, India |
| Qualification | M.Sc. in Biochemistry |
| Experience | 6.5+ Years |
| Functional Area | Quality Control / Analytical |
| Industry | Pharmaceutical / Biopharmaceutical |
| Employment Type | Full-Time |
Job Summary
The Quality Control Analyst I will be responsible for analytical and quality control activities related to stability testing, analytical method transfer, method validation, instrument calibration, and quality documentation.
The selected candidate will also work with quality and laboratory systems such as TrackWise, Glorya EDMS, and LIMS while ensuring that laboratory activities and documentation comply with applicable guidelines and procedures.
Key Responsibilities
The selected candidate will be responsible for:
- Performing stability analysis of pharmaceutical products.
- Conducting analytical method transfer activities.
- Performing analytical method validation.
- Reviewing analytical and quality control documents.
- Performing calibration and validation of laboratory instruments and equipment.
- Preparing Method Transfer Protocols (MTP).
- Preparing Method Transfer Reports (MTR).
- Preparing Methods of Analysis (MTH).
- Preparing Test Data Sheets (TDS) for stability analysis.
- Preparing documentation related to method transfer and validation.
- Ensuring analytical documentation complies with current regulatory and quality guidelines.
- Preparing departmental Standard Operating Procedures (SOPs).
- Preparing analytical validation protocols.
- Initiating quality-related forms in TrackWise.
- Managing and maintaining documents in Glorya EDMS.
- Entering stability samples into LIMS.
- Maintaining accurate laboratory and quality control records.
Educational Qualification
Candidates should possess:
M.Sc. in Biochemistry
The provided job description specifically mentions M.Sc. Biochemistry as the required educational qualification.
Experience Required
Candidates should have:
6.5+ years of relevant experience
The position is intended for experienced professionals with strong exposure to analytical laboratory and quality control activities.
Relevant experience in areas such as method validation, method transfer, stability analysis, analytical documentation, and laboratory systems will be particularly useful.
Required Skills
Candidates should have practical knowledge or experience in:
- Stability Analysis
- Analytical Method Validation
- Method Transfer
- Instrument Calibration
- Equipment Validation
- Analytical Documentation
- Method Transfer Protocols
- Method Transfer Reports
- Methods of Analysis
- Test Data Sheets
- SOP Preparation
- Validation Protocols
- TrackWise
- LIMS
- Electronic Document Management Systems
- Quality Control
- Pharmaceutical Laboratory Operations
- Regulatory Compliance
Laboratory and Quality Systems
The role requires candidates to work with multiple quality and laboratory management systems.
TrackWise
The selected candidate will be responsible for initiating relevant quality forms in TrackWise as part of quality system activities.
Glorya EDMS
The position also involves document management and maintenance through Glorya EDMS.
LIMS
Candidates will enter and manage stability sample information in LIMS, supporting laboratory sample tracking and related activities.
Stability and Analytical Method Activities
A major part of the role involves stability analysis and analytical method-related activities.
The selected professional will prepare and review documentation associated with:
- Stability testing
- Method transfer
- Method validation
- Analytical procedures
- Instrument qualification and validation
- Laboratory testing
- Quality documentation
All activities must be performed according to applicable guidelines and established company procedures.
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Salary Details
Teva has not disclosed the salary range for the Quality Control Analyst I position in the provided job description.
The final compensation may depend on the candidate’s experience, technical expertise, qualification, and interview performance.
Employee Benefits
Teva states that employees may have access to benefits and career development opportunities, which can include:
- Annual leave
- Reward programs
- Flexible working arrangements where applicable
- Health support
- Career development programs
- Learning opportunities
- Short-term projects
- Internal career opportunities
- Professional development through Teva’s career platform
Benefits may vary depending on the role and applicable company policies.
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Career Opportunity
This position can be a strong opportunity for experienced Biochemistry professionals looking to advance their careers in pharmaceutical Quality Control and Analytical Operations.
The role provides exposure to:
- Pharmaceutical stability studies
- Analytical method validation
- Method transfer
- Quality systems
- Laboratory information management
- Regulatory documentation
- Pharmaceutical quality control processes
Professionals can build further careers in Quality Control, Analytical Development, Quality Systems, Validation, and Pharmaceutical Laboratory Management.
Job Location
Chennai, Tamil Nadu, India
Job ID: 69148
How to Apply
Interested and eligible candidates can apply through Teva’s official careers portal for the Quality Control Analyst I position.
Candidates should highlight their experience in:
- Stability Analysis
- Method Validation
- Method Transfer
- Analytical Testing
- Instrument Calibration
- Quality Documentation
- TrackWise
- LIMS
- EDMS
- Pharmaceutical Quality Control
Frequently Asked Questions (FAQs)
What is the job role at Teva?
Teva is hiring for Quality Control Analyst I.
Where is the position located?
The job is based in Chennai, Tamil Nadu.
What qualification is required?
Candidates should have an M.Sc. in Biochemistry.
How much experience is required?
The position requires 6.5+ years of experience.
What are the main responsibilities?
The main responsibilities include stability analysis, analytical method transfer, method validation, instrument calibration, validation documentation, SOP preparation, TrackWise activities, EDMS document management, and LIMS sample entry.
Which systems are mentioned in the job description?
The role specifically mentions TrackWise, Glorya EDMS, and LIMS.
