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Quality Analyst Ii

5-7 years
Not Disclosed
10 Sept. 22, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Quality Analyst II

Date Posted:

16 Sept 2025

Location:

Bangalore, India, 560064

Company:

Teva Pharmaceuticals

Job ID:

63664


Company Overview:

Teva Pharmaceuticals is a global leader in generic medicines and a producer of many products on the WHO Essential Medicines List. Teva’s mission is to make healthcare more affordable and accessible, impacting millions of people worldwide. The company operates in nearly 60 countries with a diverse workforce and continues to innovate to improve global health outcomes.


Role Overview:

The Quality Analyst II provides expertise in pharmaceutical quality systems, ensuring compliance with cGxP requirements and internal quality standards. The role involves managing complex quality-related activities, supporting cross-functional teams, and maintaining electronic quality management systems.


Key Responsibilities:

  • Demonstrate in-depth knowledge of pharmaceutical quality and quality systems, with exposure to best practices.

  • Maintain compliance with cGxP requirements and support quality-related IT applications.

  • Manage complex activities and support large, cross-functional teams.

  • Use technical knowledge to operate Quality Management computer systems, including:

    • Electronic Document Management Systems (EDMS)

    • Quality Management Systems (QMS)

    • Processes such as deviations, CAPA, laboratory investigations, complaints, trends, change control, document management, notifications to health authorities and management.

  • Utilize tools such as Excel, Word, PowerPoint, MS Project, and SharePoint effectively.

  • Exhibit resourcefulness, initiative, and create urgency to meet objectives and deadlines.

  • Maintain excellent verbal and written communication skills in English.

  • Knowledge of Veeva Quality system is a plus.


Required Qualifications:

  • Bachelor’s degree in Science (advanced degree preferred in science, regulatory, computer science, or management).

  • Minimum of 5–7 years of experience in the pharmaceutical or related industry.

  • International experience and experience working with large cross-functional teams.


Skills & Competencies:

  • Strong technical expertise with quality systems and processes.

  • Ability to manage complex activities and cross-functional collaboration.

  • Attention to detail, problem-solving skills, and process-oriented mindset.

  • Proficiency in MS Office and relevant quality management software.

  • Effective communication and documentation skills.


Internal Candidates:

Current Teva employees should apply through the internal career site (“Employee Central”) for priority consideration and access to exclusive opportunities.


Equal Opportunity Statement:

Teva Pharmaceuticals is committed to equal opportunity in employment. Employment decisions are based on merit, qualifications, and business requirements without regard to age, race, religion, sex, disability, sexual orientation, gender identity, or other legally protected status. Reasonable accommodations will be provided to support candidates during recruitment.