Title: Solution Architect, D&T,SAP PLM

Requisition ID: 75079

Date: Jul 20, 2026

Location:

Bengaluru, KA, IN

Department: Digtl & Transfrmtion

Description:

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

This position is responsible for providing Design Verification & Validation for device (Include Software ,Electronics, Mechanical) , Also on computer system validation activities for Research and Development Division and Manufacturing Division in accordance with technical document creation as per the 13485-quality management system.

This is a key technical role responsible for the Medical Device Verification and Validation also responsible for Computer System Validation activities , consists of Test planning ,Design and development of Test cases & Test Scripts , Creation of Test Protocols , Execution of Test case, Scripts , Protocols , VMP,RA,IQ,OQ,PQ,VSR,TM and reporting of the NPI and Sustenance products brings quick and innovative implementation, improvement and continuous reinforcement of established Quality Assurance fundamental practices that are utilized in the local and global business.

The role involves hands-on work in the areas of Medical Devices, Software Verification and Validation and Computer System Validation.

Essential Duties and Responsibilities

Responsible for study and understanding the Software Engineer System, Manufacturing software Topology from verification and validation point of view.
Responsible for driving the End-to-End Verification and Validation phase activities includes Test planning ,Design and development of Test cases & Test Scripts (White box) , reviews ,Create and review of Test Protocols , Execution of Test case, Scripts , Protocols and reporting of the NPI and Sustenance products ( Device and System software)
Supports continuous product improvement through detailed Test and verification activities and identify the failure before the milestone release do the failure analysis for non-conformances, and investigates, communicate with the developers and implements effective and compliant solutions for product corrections from the quality point of view with remediation action plans, and for corrective and preventive actions (CAPA Program).
Supports on product efficiency and compliance effectiveness through the development and implementation of Device and software verification and validation plans and the development of detailed product process flow diagrams that describe critical interdependencies with respect to product inputs, outputs, risks and impacts as per process and product realization.
Requirement Specification (URS), Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) scripts , Trace Matrix and Validation Summary Report in accordance with the global Computer System Validation procedure.
Responsible for All Verification and Validation deliverables , Computer System Validation deliverables of NPI and Sustenance projects.
Effectively interact with the cross functional teams like Design and Development , Quality , Regulatory and Compliance teams.

Additional Responsibilities

Education

Bachelor's in Electronics and Communication or Computer Science background

Work Experience

Minimum of 3-year experience working in a medical or any regulated industry.
Ability to communicate effectively in English (both written and oral).
Demonstrated experience and proficiency with MS Office word processing, spreadsheet, presentation, and database applications.
Certification on Azure DevOps or any relevant tool and Lean or Safe Agile Is preferable.

Preferred Knowledge, Skills and Abilities

CSV
Azure DEVOPS
Modern Requirement (preferrable)

License and Certifications

Travel Requirements

10%: Up to 26 business days per year

Physical Requirements

Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.

Additional Requirements

What We Offer

Shift

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.