Quality Control Analysts Hiring Teva Pharmaceuticals
- Teva Pharmaceuticals Hiring Quality Control Analyst in Goa | M.Sc Chemistry Professionals Apply
- Company Overview
- Job Role & Responsibilities
- Quality Control Laboratory Operations
- Analytical Testing & Documentation
- Instrument & Equipment Management
- Reagent Preparation & Standardization
- Quality Systems & Compliance
- Documentation & SOP Management
- LIMS Management
- Eligibility / Qualifications
- Educational Qualification
- Eligible Specializations
- Experience Required
- Required Skills
- Quality Control Skills
- Technical Skills
- Instrument Handling
- Regulatory Knowledge
- Location & Salary
- Employee Benefits
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What qualification is required for the Quality Control Analyst role?
- 2. How much experience is required?
- 3. What systems are used in this role?
- 4. What are the key responsibilities of a Quality Control Analyst?
- 5. Is pharmaceutical industry experience mandatory?
- 6. Where is the job located?
- Job Summary
Teva Pharmaceuticals Hiring Quality Control Analyst in Goa | M.Sc Chemistry Professionals Apply
Teva Pharmaceuticals has announced a recruitment opportunity for the position of Quality Control Analyst at its Goa manufacturing facility. The company is looking for experienced Quality Control professionals with strong analytical laboratory expertise and pharmaceutical quality compliance knowledge.
This opportunity is ideal for candidates with experience in pharmaceutical quality control testing, laboratory operations, GMP compliance, LIMS, SAP, TrackWise, instrument calibration, and analytical documentation. Professionals seeking career growth in pharmaceutical quality management, analytical sciences, and regulatory-compliant laboratory environments can explore this role.
Company Overview
Teva Pharmaceuticals is one of the world’s leading biopharmaceutical companies, combining a strong generics business with innovative medicines across multiple therapeutic areas. The company focuses on improving patient access to quality healthcare solutions while maintaining high standards in pharmaceutical manufacturing, quality assurance, research, and regulatory compliance.
With operations across global markets, Teva provides employees with opportunities to work in advanced pharmaceutical environments while contributing to the development and supply of high-quality medicines worldwide.
Job Role & Responsibilities
Quality Control Laboratory Operations
- Receive, register, and maintain laboratory samples, standards, and excipients.
- Perform analytical testing according to approved schedules and testing plans.
- Execute analysis based on the analyst qualification matrix.
- Ensure compliance with laboratory procedures and quality standards.
- Support routine Quality Control operations.
Analytical Testing & Documentation
- Perform testing of pharmaceutical samples.
- Generate accurate analytical results and reports.
- Maintain timely and error-free documentation as per Good Laboratory Practices (GLP).
- Prepare laboratory records and supporting documentation.
- Ensure data integrity throughout testing activities.
Instrument & Equipment Management
- Perform calibration of laboratory instruments and equipment.
- Maintain calibration records and schedules.
- Ensure proper functioning of analytical instruments.
- Support preventive maintenance activities.
Reagent Preparation & Standardization
- Prepare laboratory reagents.
- Perform standardization of volumetric solutions.
- Maintain reagent preparation records.
- Ensure compliance with laboratory specifications.
Quality Systems & Compliance
- Submit approved analytical reports to Quality Assurance.
- Handle TrackWise Harmony system-related activities.
- Support SAP-related quality operations.
- Perform Glorya system-related activities.
- Ensure compliance with GMP, GLP, and data integrity requirements.
Documentation & SOP Management
- Revise and update Standard Operating Procedures (SOPs).
- Update analytical test methods and specifications.
- Maintain controlled quality documents.
- Support continuous improvement initiatives.
LIMS Management
- Record analytical data in Laboratory Information Management Systems (LIMS).
- Review and report results through LIMS software.
- Ensure accurate electronic documentation and traceability.
Eligibility / Qualifications
Educational Qualification
Candidates must possess:
- M.Sc Chemistry
Eligible Specializations
- Analytical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Physical Chemistry
- Pharmaceutical Chemistry
- Applied Chemistry
- Industrial Chemistry
- Medicinal Chemistry
- General Chemistry
Experience Required
- 4 to 7 years of relevant pharmaceutical Quality Control experience.
- Experience in analytical laboratory operations is required.
- Experience in regulated pharmaceutical manufacturing environments preferred.
Required Skills
Quality Control Skills
- Pharmaceutical Quality Control
- Analytical Testing
- Laboratory Operations
- GLP Compliance
- GMP Documentation
- Data Integrity Practices
Technical Skills
- LIMS Software
- SAP
- TrackWise Harmony
- Laboratory Instrument Calibration
- Analytical Method Execution
- Documentation Management
Instrument Handling
Experience with pharmaceutical analytical instruments such as:
- HPLC
- GC
- UV Spectrophotometer
- Dissolution Apparatus
- FTIR
- Laboratory Analytical Equipment
Regulatory Knowledge
- Good Laboratory Practices (GLP)
- Good Manufacturing Practices (GMP)
- Data Integrity Requirements
- Pharmaceutical Quality Systems
- Regulatory Compliance Standards
Location & Salary
Location: Goa
Salary: ₹6.5 LPA – ₹10 LPA (Approximate Industry Standard Based on Experience and Skills)
Employee Benefits
Teva offers a comprehensive employee benefits package, including:
- Medical Insurance Coverage
- OPD Benefits
- Annual Health Check-Ups
- Term Life Insurance
- Accident Insurance
- Employee Assistance Program
- Subsidized Meals
- Wellbeing Programs
- Learning & Development Opportunities
- Mentorship Programs
- Global Career Growth Opportunities
- AI-Enabled Learning Programs
- Community Engagement Initiatives
Application Process
Interested candidates can apply through the official Teva Careers portal.
Apply Here: https://careers.teva/job/Goa-Quality-Control-Analyst-Indi-403722/1388444700/
Frequently Asked Questions (FAQs)
1. What qualification is required for the Quality Control Analyst role?
Candidates must possess an M.Sc in Chemistry or a relevant chemistry specialization.
2. How much experience is required?
Applicants should have 4 to 7 years of pharmaceutical Quality Control experience.
3. What systems are used in this role?
The position involves working with LIMS, SAP, TrackWise Harmony, and other laboratory quality systems.
4. What are the key responsibilities of a Quality Control Analyst?
Responsibilities include analytical testing, documentation, calibration, SOP management, quality system activities, and laboratory compliance.
5. Is pharmaceutical industry experience mandatory?
Yes. Relevant experience in pharmaceutical Quality Control laboratories is required.
6. Where is the job located?
The position is based in Goa, India.
Job Summary
| Category | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Department Vacancies | Quality Control Analyst |
| Qualification | M.Sc Chemistry |
| Experience | 4–7 Years |
| Location | Goa |
To apply for this job please visit careers.teva.
