Job Description

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