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Assoc Dir Global Quality Function - 3544

0-2 years
Not Disclosed
10 Nov. 18, 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

Associate Director – Global Quality Function (Fresher / Entry-Level Opportunity)

Location: Bangalore, India – 560064
Category: Quality Assurance / Pharmaceutical Manufacturing / Global Compliance
Job Type: Full-Time
Experience Required: Fresher / 0–2 Years
Job ID: 64643


Company Overview

Teva Pharmaceuticals is a global leader in the pharmaceutical industry, committed to making healthcare more affordable and accessible. Operating in nearly 60 countries, Teva produces generic and specialty medicines that improve the lives of millions worldwide, including products listed on the World Health Organization’s Essential Medicines List.

This role offers freshers an opportunity to start a career in global pharmaceutical quality assurance, gaining hands-on exposure to quality management systems, regulatory compliance, and cross-functional collaboration in a multinational environment.


Role Overview

The Associate Director – Global Quality Function supports the execution of Product Quality Reviews (PQRs), Annual Product Reviews (APRs), and regulatory documentation in alignment with Teva’s CORP Quality Management System (QMS). Entry-level candidates will learn to support global quality functions, coordinate with manufacturing sites, and contribute to compliance and process improvement initiatives.

Key focus areas include:

  • Product quality reviews and approvals

  • Data migration and accuracy

  • Collaboration with Global R&D and Commercial affiliates

  • Maintenance of quality management systems and SOPs

  • Supporting training and performance monitoring initiatives


Key Responsibilities

Product Quality Reviews (PQRs) & Annual Product Reviews (APRs)

  • Support review and compilation of PQRs/APRs prepared by team members.

  • Assist in identifying and escalating quality issues and CAPA actions.

  • Ensure alignment of reviews with external and internal stakeholders.

  • Learn to manage review processes for outsourced and in-house products.

Data Migration & R&D CMC Documentation

  • Assist in timely and accurate data migration across systems.

  • Support review of CMC documents in collaboration with Global R&D.

  • Escalate issues to senior management as required.

Quality Management Systems

  • Contribute to maintaining the local and global Quality Management System (QMS).

  • Assist in process changes, deviations, SOP approvals, and compliance checks.

  • Gain experience ensuring alignment with regulatory guidelines (cGxP).

Performance Management & Training

  • Support monitoring of KPIs and departmental performance metrics.

  • Assist in training initiatives, including GMP and on-the-job training.

  • Participate in monthly quality councils and team effectiveness reviews.

Miscellaneous Support

  • Assist with hiring and employee data management.

  • Support finance-related activities for departmental budgets and POs.

  • Aid in reporting and communication with higher management.


Qualifications & Skills

Education:

  • Bachelor’s degree in Pharmacy, Chemistry, Biology, or Life Sciences.

  • Master’s degree preferred but fresh graduates are encouraged to apply.

Experience:

  • Fresher / 0–2 years, including internships, academic projects, or exposure to quality systems.

Skills:

  • Basic knowledge of cGxP regulations, QA/QC processes, and global compliance standards.

  • Understanding of pharmaceutical manufacturing, contract manufacturing, and quality operations.

  • Familiarity with IT systems such as TrackWise, SAP, LIMS, or similar platforms.

  • Strong communication, organizational, and problem-solving skills.

  • Willingness to learn and support a matrixed, global team environment.


Why Join Teva Pharmaceuticals?

  • Launch a career in global pharmaceutical quality management with structured mentorship.

  • Gain exposure to international regulatory standards and cGxP compliance.

  • Work with cross-functional teams in a global, collaborative environment.

  • Opportunity for continuous growth into leadership roles in QA and regulatory compliance.


Equal Employment Opportunity

Teva Pharmaceuticals is committed to a diverse and inclusive workplace. Employment decisions are made without regard to age, race, religion, sex, disability, sexual orientation, gender identity, veteran status, or any other legally protected status. Accommodations are provided for candidates requiring support during the recruitment process.