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Associate Manager-Quality Investigation

6+ years
Not Disclosed
10 Sept. 15, 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 Role: Associate Manager – Quality Investigation

📍 Location: India – Vizag (On-Premise)
💼 Job Type: Full-time
🆔 Job ID: 4938779
📅 Posted: 3 Days Ago


About Pfizer

Pfizer’s purpose is to deliver Breakthroughs that change patients’ lives.

  • Values: Guided by four core values that define what Pfizer achieves and how it is achieved.

  • Division: Pfizer Global Supply (PGS) – responsible for manufacturing and distributing Pfizer’s pharmaceutical products.


Role Purpose

This role ensures the investigation and resolution of quality issues in manufacturing and quality laboratories. By applying scientific, risk-based, and customer-oriented approaches, the Associate Manager plays a vital role in delivering safe and effective products to patients.


Key Responsibilities

  • Investigate quality issues in manufacturing and quality laboratories.

  • Conduct investigations into deviations, out-of-specification (OOS) results, and atypical cases.

  • Identify root causes and recommend corrective action plans.

  • Ensure compliance of all reports with regulatory requirements and Pfizer policies.

  • Contribute to moderately complex projects, managing time and deliverables effectively.

  • Develop and execute plans for short-term activities in collaboration with team members.

  • Apply technical knowledge and skills to support team objectives.

  • Make decisions to resolve moderately complex problems within standard procedures.

  • Work under general supervision, following established procedures and guidelines.


Basic Qualifications

  • Education: B.Pharm / M.Pharm / M.Sc.

  • Experience: Minimum 6 years in the pharmaceutical industry.

  • Proven record of problem-solving and decision-making.

  • Strong knowledge of manufacturing, compliance, technology investigations, processes, and systems.

  • Ability to work independently as well as collaboratively.

  • Excellent written and verbal communication skills.

  • Strong computer skills, with proficiency in Excel spreadsheet management.


Preferred Qualifications

  • Experience conducting and writing investigations using structured methodologies.

  • Familiarity with regulatory requirements and quality standards.

  • Strong analytical and critical thinking capabilities.

  • Ability to manage multiple projects simultaneously.

  • Experience with root cause analysis (RCA) and corrective action planning.

  • Excellent organizational and mentoring skills.

  • Strong interpersonal skills and ability to foster a collaborative team culture.


Work Location

  • Assignment: On-Premise


Job Category

Quality Assurance and Control