Kwality Pharmaceuticals Ltd. is hiring experienced professionals for the QA Validation Department at its Oncology/Cytotoxic Injectable Plant in Jassur, Nurpur, Himachal Pradesh.

Job Information

Company Name: Kwality Pharmaceuticals Ltd.
Department: Quality Assurance (QA Validation) – Oncology/Cytotoxic Plant
Location: Jassur, Nurpur, Himachal Pradesh
Position: Officer / Sr. Executive / Assistant Manager – QA Validation

Education Qualification

• B.Pharm
• M.Pharm
• M.Sc.
• Equivalent qualification in a relevant discipline

Experience Required

Officer

• 3 to 6 years of experience in Pharmaceutical QA/Validation

Sr. Executive / Assistant Manager

• 10+ years of experience in Pharmaceutical QA/Validation

Preferred: Candidates with experience in Cytotoxic Injectable Manufacturing.

Technical Skills Required

• Terminal Sterilization Validation
• Lyophilizer Qualification & Validation
• Isolator Qualification & Validation
• Aseptic Processing
• Process Validation
• Cleaning Validation
• Equipment Qualification (DQ, IQ, OQ, PQ)
• Autoclave Qualification
• Media Fill Studies
• HVAC & Cleanroom Qualification
• GMP
• Data Integrity
• QMS
• CAPA
• Change Control

Job Responsibilities

• Prepare and review validation protocols and reports.
• Perform DQ, IQ, OQ and PQ activities.
• Handle sterilizer, lyophilizer and isolator validation.
• Execute process and cleaning validation activities.
• Review validation data and reports.
• Manage deviations, CAPA and change controls.
• Coordinate with Production, QC and Engineering teams.
• Ensure GMP and Data Integrity compliance.
• Support internal and regulatory audits.
• Maintain validation documentation and records.

How to Apply

Email: hrd.hp@kwalitypharma.com

Mobile: 9149805912

Subject Line: Application – QA Validation – Oncology Plant

FAQs

1. What is QA Validation?

QA Validation ensures pharmaceutical processes and equipment consistently produce quality products according to regulatory requirements.

2. What are DQ, IQ, OQ and PQ?

These are qualification stages used to verify equipment design, installation, operation and performance.

3. What is Process Validation?

Process Validation confirms that a manufacturing process can consistently produce products meeting quality standards.

4. What is Media Fill Validation?

Media Fill is a simulation study used to verify the effectiveness of aseptic manufacturing processes.

5. Why is Cleaning Validation important?

Cleaning Validation ensures equipment is properly cleaned and prevents product contamination and cross-contamination.

Apply now and join Kwality Pharmaceuticals’ Quality Assurance team in the Oncology/Cytotoxic Injectable Manufacturing Division.