Exciting pharma jobs alert! Kwality Pharmaceuticals Ltd is hiring for Quality Assurance, Quality Control, Microbiology, and Injectable Production roles. Join this growing pharmaceutical company through a walk-in drive on 12th April 2026. Perfect opportunity for experienced professionals seeking pharmaceutical careers in India.
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About the Company
Kwality Pharmaceuticals Ltd., established in 1983 and headquartered in Amritsar, Punjab, is a leading Indian pharmaceutical manufacturer and exporter of finished formulations. With facilities in Amritsar and Kangra (Himachal Pradesh), the company specializes in niche molecules, including injectables, using advanced technologies.
It holds WHO-GMP, EU-GMP, and various international approvals, exporting to over 80 countries across Asia, Africa, and beyond. Committed to innovation, quality, and regulatory compliance, Kwality Pharma focuses on affordable, high-quality healthcare solutions while maintaining state-of-the-art infrastructure and strong R&D capabilities.
Job Details
- Company Name: Kwality Pharmaceuticals Ltd.
- Experience: 2–8 years (varies by role)
- Qualification: B.Pharma, M.Pharma, MSc, BSc/MSc Microbiology, B.Tech Biotech
- Location: Amritsar and Kangra
- Work Type: On-site
Job Description
Kwality Pharmaceuticals Ltd. is expanding its team and inviting applications for multiple positions in Quality Assurance, Quality Control, Microbiology, and Production (Injectables) departments. These roles support the company’s commitment to manufacturing niche pharmaceutical products under stringent global standards.
Candidates with relevant experience in QMS, validation, analytical techniques, sterility testing, and aseptic processing are encouraged to apply.
Quality Assurance (QA) Roles
- Position Title: Officer / Sr. Officer / Executive / Sr. Executive
- Department: Quality Assurance
- Role: QMS, Qualification & Validation (Process Validation, Utility, Injectables), IPQA
- Experience: 2–8 years
- Education/Qualification: MSc, B.Pharma, M.Pharma
Quality Control (QC) Roles
- Position Title: Officer / Sr. Officer / Executive / Sr. Executive
- Department: Quality Control
- Role: HPLC (RM, PM, FG), Analytical Method Validation (AMV)
- Experience: 2–6 years
- Education/Qualification: MSc, B.Pharma, M.Pharma, B.Tech Biotech
Microbiology (Micro) Roles
- Position Title: Executive / Sr. Executive / Officer / Sr. Officer
- Department: Microbiology
- Role: Environmental Monitoring (EM), BET, MLT, QMS, Sterility Testing
- Experience: 2–8 years
- Education/Qualification: BSc/MSc Microbiology / Biotech, B.Pharma
Production (Injectable) Roles
- Position Title: Officer / Sr. Officer / Executive / Sr. Executive
- Department: Production (Injectable)
- Role: QMS, Filling, Sealing, Aseptic Processing
- Experience: 2–8 years
- Education/Qualification: B.Pharma, M.Pharma
Skills/Qualifications
- Strong knowledge of Quality Management System (QMS) and regulatory compliance
- Expertise in process/utility/equipment qualification and validation
- Hands-on experience with HPLC, analytical method validation, and stability studies
- Proficiency in microbiological testing including BET, MLT, sterility, and environmental monitoring
- Understanding of aseptic filling, sealing, and injectable manufacturing processes
- Ability to handle documentation, investigations, and CAPA in a cGMP environment
- Team player with good communication and problem-solving skills
Key Responsibilities
- Execute IPQA and in-process quality checks as per SOPs
- Perform analytical testing using HPLC for raw materials, packaging, and finished goods
- Conduct environmental monitoring, BET, MLT, and sterility tests
- Manage process validation, utility qualification, and equipment validation
- Oversee aseptic filling, sealing, and production activities in injectable areas
- Ensure timely documentation, deviation handling, and compliance with QMS
- Support regulatory audits and maintain cGMP standards
Benefits/Perks
- Career growth in a fast-expanding pharmaceutical company
- Opportunities for learning advanced technologies and global best practices
- Competitive salary packages commensurate with experience
- Professional work culture focused on quality and innovation
- Exposure to international regulatory standards and global markets
How to Apply
Share your updated CV via email on career@kwalitypharma.com or contact the recruitment team directly:
- +91-98374-54653
- +91-99157-60166
For more pharmaceutical job opportunities across India, visit PharmaRecruiter.in.
Apply now and take the next step in your pharma career!
Walk-in Interview Details
- Date: Sunday, 12th April 2026
- Time: 9:00 AM to 5:00 PM
- Venue: Hotel Akash, Pathankot-Jammu National Highway, Kalibari, Kathua 184104
- Contact/Email: career@kwalitypharma.com | +91-98374-54653 | +91-99157-60166
Candidates are advised to carry all relevant documents, including educational certificates, experience letters, and a copy of their CV.
Why You Should Join
Joining Kwality Pharmaceuticals Ltd. means becoming part of a company recognized for its quality, innovation, and global reach. With a legacy since 1983, the organization offers long-term career stability in a supportive environment that values compliance, continuous learning, and professional growth.
Employees benefit from working with cutting-edge technologies in WHO-GMP and EU-GMP approved facilities while contributing to affordable healthcare solutions worldwide.
FAQs
Q1: What is the minimum experience required for these pharma jobs?
A: Most positions require 2–8 years of relevant experience, depending on the role and level.
Q2: Which qualifications are accepted for QA/QC/Micro/Production roles?
A: B.Pharma, M.Pharma, MSc, BSc/MSc in Microbiology or Biotechnology, and B.Tech Biotech are preferred.
Q3: Is prior injectable or aseptic experience mandatory?
A: Experience in injectable production, QMS, validation, or sterility testing is highly advantageous, especially for Production and Micro roles.
Q4: Are there growth opportunities at Kwality Pharmaceuticals Ltd.?
A: Yes, the company is expanding rapidly and offers excellent career progression in quality and manufacturing functions within a regulated, innovative environment.
