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Manager Quality Assurance – Pharmaceutical Manufacturing & Validation

Abbott
Abbott
3-4 years
Not Disclosed
Baddi, India
1 May 8, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Manager Quality Assurance – Pharmaceutical Manufacturing & Validation Job in Baddi, India

Company: Abbott Laboratories
Job Title: Manager Quality Assurance
Location: Baddi, Himachal Pradesh, India
Department: Quality Assurance
Industry: Pharmaceutical Manufacturing / Hormone Facility
Job Type: Full-Time


About Abbott

Abbott is a globally recognized healthcare and pharmaceutical company committed to delivering high-quality healthcare solutions, innovative medicines, diagnostics, and medical technologies. With a strong presence across global markets, Abbott continues to drive excellence in pharmaceutical manufacturing, quality systems, and regulatory compliance.

The company offers professionals a collaborative environment, advanced manufacturing exposure, and strong career growth opportunities within the healthcare and life sciences industry.


Job Overview

Abbott is seeking an experienced Manager Quality Assurance for its Hormone Manufacturing Facility located in Baddi, India. The role involves leading quality assurance operations, validation activities, GMP compliance, process quality oversight, batch release management, and quality management system (QMS) operations within a regulated pharmaceutical manufacturing environment.

The selected candidate will play a critical role in ensuring compliance with current Good Manufacturing Practices (cGMP), data integrity standards, validation protocols, and internal quality systems while supporting continuous process improvement and audit readiness.

This opportunity is ideal for experienced pharmaceutical quality professionals with expertise in manufacturing quality assurance, process validation, QMS management, and regulatory compliance.


Experience Required

Experience Level

  • Mid-Level to Senior-Level Quality Assurance Professional
  • Freshers are not eligible

Preferred Experience

  • Experience in:
    • Pharmaceutical Quality Assurance
    • Hormone Manufacturing Facilities
    • GMP Compliance
    • Process Validation
    • Cleaning Validation
    • Batch Release
    • QMS Operations
    • Internal Audits

Technical Exposure Required

  • Compression Machines
  • Isolators
  • Blenders
  • Bulk Packing Lines
  • Manufacturing & Packaging Operations

Educational Qualification

Required Qualification

Candidates must possess any of the following:

  • M.Pharm
  • B.Pharm
  • M.Sc.

Key Responsibilities

Quality Assurance Operations

  • Ensure compliance with:
    • Current Good Manufacturing Practices (cGMP)
    • Good Documentation Practices (GDP)
    • Data Integrity requirements
  • Monitor quality assurance activities across the Hormone Facility