Kwality Pharmaceuticals Ltd. is inviting applications from qualified and experienced professionals for its EU-GMP Certified Manufacturing Sites. The company is hiring candidates for the Research & Development (R&D) department, specifically in Analytical Method Development & Validation (ADL). This is an excellent opportunity for B.Pharm and M.Pharm graduates looking to advance their careers in pharmaceutical research and analytical development.

Job Details

Department: Research & Development (R&D)

Position: Officer / Executive

Role: Analytical Method Development & Validation (ADL)

Experience Required: 1–4 Years

Qualification: B.Pharm / M.Pharm

Key Responsibilities

• Perform Analytical Method Development (AMD) and Method Validation activities.

• Develop and validate analytical methods in compliance with regulatory requirements.

• Prepare analytical documentation and reports.

• Follow cGMP and laboratory quality standards.

• Coordinate with cross-functional teams to ensure timely completion of analytical projects.

Why Join Kwality Pharmaceuticals?

• Work at EU-GMP Certified manufacturing facilities.

• Innovative and collaborative work culture.

• Career growth and professional development opportunities.

• Employee well-being initiatives.

• Exposure to advanced pharmaceutical research and analytical technologies.

How to Apply

Interested candidates can send their updated CV through the following channels:

Email: career@kwalitypharma.com

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Open Positions

• Officer – Quality

• Senior Officer – Quality

• Executive – Quality

Job Location

1-A Industrial Area, Nurpur, Raja Ka Bagh, Himachal Pradesh – 176201

Experience Required

• 1–6 Years

Mandatory Skill

Candidates should have hands-on experience in HPLC (High-Performance Liquid Chromatography).

Key Requirements

• Experience in the pharmaceutical industry.

• Strong knowledge of HPLC analysis, operation, troubleshooting, and documentation.

• Good understanding of cGMP, GLP, and regulatory guidelines.

• Strong analytical and documentation skills.

• Ability to maintain quality documentation and ensure compliance with pharmaceutical standards.

How to Apply

Interested candidates can share their updated CV at:

Email: hrd.hp@kwalitypharma.com