QA Equipment Validation Jobs – QA Executive / Manager

Location: Baddi
Experience: 3–5 Years
Department: Quality Assurance
Industry: Pharmaceutical – Injectable / Sterile Manufacturing
Qualification: B.Pharm / M.Pharm / B.Tech / M.Tech
Employment Type: Full-Time

Job Overview

Are you looking for QA Equipment Validation Jobs in the pharmaceutical industry? ACME HR Consulting is looking for skilled QA professionals for an Equipment Validation position in the pharmaceutical injectable and sterile manufacturing sector.

The ideal candidate should have 3–5 years of experience in Quality Assurance (QA), equipment qualification and validation activities. Candidates should possess practical knowledge of GMP guidelines, validation documentation, equipment qualification protocols and regulatory compliance.

This opportunity is suitable for professionals who have experience in sterile or injectable pharmaceutical manufacturing and want to advance their careers in Quality Assurance.

Key Responsibilities

• Prepare, review and approve User Requirement Specifications (URS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) documents.
• Coordinate equipment qualification activities for manufacturing and utility equipment.
• Prepare and review equipment validation protocols and reports.
• Review validation documents, deviations, change controls and CAPA related to qualification activities.
• Ensure compliance with Good Manufacturing Practices (GMP), regulatory guidelines, SOPs and data integrity requirements.
• Coordinate with Engineering, Production, Quality Control (QC) and Quality Assurance (QA) departments.
• Support internal, customer and regulatory audits related to equipment qualification.
• Maintain validation records and ensure timely completion of validation schedules.
• Participate in risk assessments and periodic equipment review and requalification activities.

Required Skills for QA Equipment Validation Jobs

Candidates applying for QA Equipment Validation Jobs should have knowledge and practical exposure to:

• Equipment Qualification and Validation
• Installation Qualification (IQ)
• Operational Qualification (OQ)
• Performance Qualification (PQ)
• User Requirement Specification (URS)
• Design Qualification (DQ)
• Good Manufacturing Practices (GMP)
• Validation Documentation
• Risk Assessment
• Change Control Management
• Deviation and CAPA Management
• Sterile and Injectable Manufacturing
• Audit Readiness
• RM Testing, Specifications (SPEC) and COA

Eligibility Criteria

• B.Pharm, M.Pharm, B.Tech, M.Tech or equivalent relevant qualification.
• 3–5 years of experience in QA or Equipment Validation.
• Experience in sterile/injectable pharmaceutical manufacturing is preferred.
• Good understanding of equipment qualification and validation procedures.
• Strong documentation and coordination skills.

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