Validation Engineer

About Us
Pharmaval Pvt Limited is a Bangalore-based consulting and engineering firm specializing in Quality, Compliance, and Validation Solutions for the Pharmaceutical, Biopharmaceutical, and Life Sciences industries. We work as an extension of our clients’ teams, helping them achieve regulatory compliance, operational excellence, and robust quality systems across their manufacturing and research facilities.

What We Do
Our core expertise includes:

• Commissioning, Qualification & Validation (CQV)
• Quality Management Systems & Risk Assessment
• Regulatory Compliance & Audit Readiness
• Project Management and Change Control
• Computer System Validation (CSV) and Data Integrity
• Training and Process Optimization

We have successfully supported projects for leading organizations across India and globally, ensuring alignment with cGMP as per WHO, USFDA, MHRA, and EU regulatory standards.

Why Join Us
At Pharmaval, we believe in scientific rigor, practical innovation, and collaborative growth. As a part of our team, you’ll gain exposure to diverse projects, cutting-edge technologies, and global quality systems — all within a dynamic environment that encourages professional development and hands-on learning.

Head Office: Bengaluru, Karnataka

Job Summary
The Validation Engineer must background in developing life-cycle documents for equipment, process and utility equipment's supporting API & Formulation operation in pharma domain . The person is responsible for the development of documents as part of validation deliverables for a project. In execution of these responsibilities, the Quality Validation Specialist should have strong testing, writing and validation skills relevant to equipment, process and utilities w.r.t to bio/pharma industry.Responsibilities and Duties

• Generate validation plans, protocols and reports that support the qualification and validation of systems.
• Generate User Requirement Specifications (URS), Functional Specifications for process equipment/ utilities
• Generate Risk Assessment Documents
• Compile data for completed validation and prepare final report packages by summarizing the data.
• Investigate deviations, write investigation reports and create summary reports.

Qualifications and Skills

• Bachelor's Degree; scientific background preferred
• At least 2-4 years of pharmaceutical validation experience
• Good knowledge of GMPs and experience in generating validation documents (IQ,OQ,PQ) as per relevant industry regulations and guidance
• Strong interpersonal skills and demonstrated ability work independently
• Organized and task oriented
• Excellent written and oral communication skills especially on technical topics
• Proficient with MS Office tools

Job Type: Full-time

Pay: ₹25,000.00 - ₹35,000.00 per month

Benefits:

• Health insurance
• Paid time off

Ability to commute/relocate:

• Bengaluru, Karnataka: Reliably commute or planning to relocate before starting work (Preferred)

Education:

• Bachelor's (Preferred)

Experience:

• CGMP: 2 years (Required)
• Document management: 2 years (Preferred)

Language:

• Kannada & Hindi (Preferred)

Work Location: In person

Expected Start Date: 03/11/2025