PHARMAFull-time
Quality Specialist II
By Admin · Quality Assurance & Quality Control
BANGALORE (India)ONSITEPOSTED: 9/12/2026
PHARMAFull-time
HIRING ORGANIZATIONTEVA PHARMACEUTICALSBiopharmaceuticals / Life Sciences
ROLE OVERVIEW
Quality Specialist II responsible for pharmaceutical quality activities including CMC documentation review, analytical method and stability documentation, equipment qualification, BMR review, and Product Quality Review/Annual Product Review activities.
ROLE DEFINITION & RESPONSIBILITIES
- •Review CMC documentation in a timely and compliant manner
- •review method development and validation protocols/reports
- •review stability protocols/reports
- •review instrument and equipment qualification records
- •review BMRs
- •compile and approve PQR/APRs
- •retrieve quality and regulatory data from databases and systems
- •coordinate with global manufacturing, QA/QC and contract manufacturing teams
- •recommend continuous quality improvement actions.
Reporting Hierarchy: Receives guidance from Supervisor, Group Leader, Manager Global Quality Services, Associate Director Global Quality GBS, and other Quality Strategy & Shared Services, EMSO Quality, Commercial Quality and TGO stakeholders.
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- 2-8 years of QA/QC experience in the pharmaceutical industry
- Master’s degree in Pharmacy or natural sciences or Bachelor’s degree in Pharmacy or natural sciences
- basic knowledge of worldwide cGxP regulations
- good English communication skills
- basic computerized systems knowledge
- understanding of manufacturing, QC and contract manufacturing processes
- hands-on analytical method development/validation and stability experience
- experience reviewing qualification records, BMRs and Product Quality Reviews.
PREFERRED QUALIFICATIONS
- •Knowledge of Teva IT systems such as TrackWise, SAP, LIMS, Global Insights and Glorya
- •additional language skills
- •stronger experience with pharmaceutical quality systems and global quality operations.
REQUIRED VERIFIED SKILLS
Pharmaceutical QA/QC; CMC documentation review; cGxP; analytical method development; method validation; stability studies; instrument/equipment qualification; BMR review; PQR/APR; quality management systems; computerized systems; communication; data review; continuous improvement
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Generous annual leave; reward plans; flexible working schedules dependent on role; tailored health support; community involvement; career development through Twist platform; learning programs; short-term projects; internal growth opportunities
No salary range is disclosed in the posting.
ORGANIZATION CONTEXT & CULTURE
Teva is a leading innovative biopharmaceutical company supported by a major generics business, focused on delivering medicines and improving health worldwide.
TEAM SIZE: 50,000+
INDUSTRY: Biopharmaceuticals / Life Sciences
Culture: High-performing and inclusive culture; fresh thinking and collaboration; employee wellbeing; flexibility; global teamwork; continuous improvement; Teva EVP pillars emphasize caring, togetherness and fulfilling work.
EXPECTED CAREER ROADMAP
Teva's Twist career development platform provides learning programs, short-term projects and internal growth opportunities, supporting employees in shaping their career paths.
APPLICATION ADVISORY
Emphasize pharmaceutical QA/QC experience, CMC documentation review, analytical method validation, stability studies, BMR/PQR/APR experience, cGxP knowledge, and familiarity with computerized quality systems.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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