PHARMAFull-time
Quality Control Technician III
By Admin · Quality Assurance & Quality Control
GOA (IN)ONSITEPOSTED: 9/4/2026
PHARMAFull-time
HIRING ORGANIZATIONTEVA PHARMACEUTICALSBiopharmaceuticals / Life Sciences
ROLE DEFINITION & RESPONSIBILITIES
Role Overview
Join Teva's Nitrosamine team at the Watson Pharma Pvt. Ltd. Goa facility.
Support analytical activities related to nitrosamines in pharmaceutical delivery systems, with a focus on patient safety, product quality, and regulatory compliance.
Work in a collaborative laboratory environment while developing expertise in analytical science.
Core Responsibilities
Develop and validate analytical methods for nitrosamine-related activities using LCMS, GCMS, and IC under guidance from senior team members.
Manage samples received from different sites for the Nitrosamine project.
Perform testing of samples for nitrosamine-related activities.
Troubleshoot analytical instruments and address day-to-day operational difficulties, escalating complex issues when required.
Maintain laboratory prerequisites including columns, standards, chemicals, spares, and consumables.
Prepare analytical protocols, reports, and technical documentation in accordance with regulatory standards.
Conduct routine instrument operation, calibration, and maintenance.
Maintain accurate instrument-usage records, calibration records, and compliance documentation.
Follow EHS requirements and maintain safe laboratory practices.
Ensure laboratory compliance and data integrity during routine operations.
Participate in internal audits and contribute to readiness for external regulatory inspections.
Technical & Analytical Expertise
Strong analytical chemistry knowledge, particularly analytical method development and validation.
Specialized knowledge of nitrosamine impurities in drug substances and drug products.
Experience with LCMS, GCMS, and ion chromatography (IC).
Ability to perform literature searches to support analytical method development.
Understanding of pharmaceutical Quality Systems and ICH guidelines.
Experience working under cGMP/GLP environments and maintaining regulatory-compliant documentation.
Systems & Software
Familiarity with computerized systems such as TrackWise and Veeva Vault.
Mass Hunter Software experience is desirable.
Experience maintaining instrument records, calibration information, analytical documentation, and data-integrity requirements.
Qualifications & Experience
M.Sc. in Chemistry or M.Pharm required.
3–5 years of hands-on experience in analytical method development and validation.
Strong logical approach and attention to detail.
Good written and oral communication skills.
Ability to work effectively within a team.
Quality, Compliance & Safety
Maintain laboratory compliance and data integrity throughout daily activities.
Follow cGMP/GLP and applicable regulatory expectations.
Support internal audits and external-inspection readiness.
Follow EHS requirements and safe laboratory practices.
Benefits & Career Development
Teva states that employees receive benefits including generous annual leave, reward plans, flexible working schedules where applicable, tailored health support, and community-giving opportunities.
Career development is supported through Teva's Twist platform, offering learning programs, short-term projects, and internal growth opportunities.
Teva emphasizes employee wellbeing, career exploration, skill development, and internal mobility.
REQUIRED VERIFIED SKILLS
M.Sc. Chemistry or M.Pharm
3-5 years analytical method development and validation
Analytical Chemistry
Nitrosamine impurity analysis
Drug substance and drug product testing
LCMS
GCMS
Ion Chromatography
Analytical method development
Analytical method validation
Literature search
cGMP
GLP
Pharmaceutical Quality System
ICH guidelines
Regulatory-compliant documentation
Data integrity
Instrument calibration and maintenance
Laboratory compliance
EHS
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
The job posting does not disclose a specific salary range, bonus amount, or numerical compensation package. Teva states that its benefits include annual leave, reward plans, flexible working schedules where applicable, tailored health support, and other employee-support programs. Actual compensation should be confirmed through the official recruitment process and will depend on experience, qualifications, role level, and location.
ORGANIZATION CONTEXT & CULTURE
Teva Pharmaceuticals is actively hiring for this position.
INDUSTRY: Biopharmaceuticals / Life Sciences
EXPECTED CAREER ROADMAP
This role can provide progression within Quality Control, Analytical Development, pharmaceutical quality, and specialized impurity testing. Hands-on exposure to nitrosamine analytical methods, LCMS/GCMS/IC, method validation, regulatory documentation, data integrity, and inspection readiness can support advancement into senior analytical/QC positions, analytical method development roles, laboratory leadership, quality systems, or specialized regulatory-compliance functions. Teva's Twist career-development platform also provides access to learning programs, short-term projects, and internal growth opportunities.
APPLICATION ADVISORY
Highlight 3–5 years of hands-on analytical method development and validation experience. Put M.Sc. Chemistry or M.Pharm prominently on the resume. Emphasize direct experience with nitrosamine impurities in drug substances/drug products and analytical techniques such as LCMS, GCMS, and IC. Include specific examples of method development, validation, troubleshooting, calibration, sample testing, analytical protocols, reports, and regulatory documentation. Mention cGMP/GLP, ICH guidelines, pharmaceutical Quality Systems, data integrity, audits, and inspection readiness. Add TrackWise, Veeva Vault, and Mass Hunter if genuinely experienced. Prepare for technical questions on nitrosamine analysis, analytical method validation, LCMS/GCMS principles, chromatography, troubleshooting, data integrity, laboratory compliance, and regulatory expectations. This is not a fresher position because the posting explicitly requires 3–5 years of hands-on experience.
RECOMMENDED TRAINING
1/5
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