Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Assistant Manager – Ipqa

Lambda Research Accelerated
Lambda Research accelerated
7+ years
INR 10 LPA – 15 LPA
Ahmedabad, India
1 May 8, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Assistant Manager – IPQA Job in Ahmedabad | Lambda Therapeutic Research Careers

Company: Lambda Therapeutic Research Ltd.
Job Title: Assistant Manager – IPQA
Job ID: 1466
Location: Ahmedabad, Gujarat, India
Job Type: Full-Time
Industry: Pharmaceutical / Biologics / Quality Assurance / CDMO
Salary Range: INR 10 LPA – 15 LPA


About Lambda Therapeutic Research Ltd.

Lambda Therapeutic Research Ltd. is a leading Contract Development and Manufacturing Organization (CDMO) focused on biologics drug development, GMP manufacturing, and First-in-Human (FIH) clinical trial support. The company provides integrated end-to-end solutions for biologics and biosimilars development through advanced infrastructure, agile project execution, and global-quality manufacturing systems.

Lambda Therapeutic Research offers professionals an innovation-driven environment with strong exposure to biologics manufacturing, GMP quality systems, pharmaceutical compliance, and advanced CDMO operations.


Job Overview

Lambda Therapeutic Research Ltd. is hiring an Assistant Manager – IPQA (In-Process Quality Assurance) for its Ahmedabad facility. The selected candidate will be responsible for overseeing shop-floor quality assurance activities, GMP compliance monitoring, QMS implementation, batch record review, deviation investigations, CAPA management, audit support, and cross-functional quality coordination.

The role requires strong expertise in pharmaceutical manufacturing quality systems, GMP documentation practices, investigation handling, and compliance management within biologics or pharmaceutical manufacturing environments.

This opportunity is ideal for experienced Quality Assurance professionals with expertise in IPQA, GMP operations, audit handling, and pharmaceutical manufacturing compliance.


Experience Required

Experience Level

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

Required Experience

  • Minimum 7 years of industrial experience in:
    • Quality Assurance (QA)
    • In-Process Quality Assurance (IPQA)
    • Manufacturing Operations
    • Quality Control
    • Engineering & Development

Preferred Industry Experience

  • Pharmaceutical Industry
  • Biologics Manufacturing
  • CDMO Operations
  • GMP Manufacturing Facilities

Educational Qualification

Required Qualification

Candidates should possess any of the following qualifications:

  • B.Pharm
    OR
  • Postgraduate Degree in:
    • Microbiology
    • Quality Assurance
    • Biochemistry
    • Biotechnology