Title: Product Engineer,R&D

Requisition ID: 74419

Date: May 25, 2026

Location:

Bengaluru, KA, IN

Department: R&D

Description:

Job Summary

The Assoc, Product Engineer will be responsible for executing development and sustainment activities of handheld and wearable drug delivery systems This role has frequent interactions with West's medical device customers and requires close collaboration with Platform Development, Quality, Regulatory Affairs, Manufacturing, Account Management. The individual will leverage their excellent problem-solving acumen, analytical, project management, solving customer service and engineering abilities to effectively drive the development and maintenance of West medical devices.

Essential Duties and Responsibilities

Lead the creation and maintenance of customer specific design history files (DHF) including product requirements, design inputs, trace matrix, design outputs, design verification, and risk management.
Ensure on-market products maintain compliance with industry standards, West QMS and agreed to customer requirements.
Lead product change control requests including conducting impact assessments, updating DHF documentation, conducting engineering and/or verification testing and review of risk documents.
Act as the primary point of contact for product specific inquiries and requests from customers
Facilitate assessment and implementation of customer (internal and external) product requests. Serves as the interface between the customer’s technical team and West’s technical team for on-market products.
Accountable for identifying, investigating and analyzing problems with product design and recommend solutions.
Prepare reports and presentations for internal, external, and cross-functional teams.
Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
Exhibits regular, reliable, punctual and predictable attendance.
Performs other duties as assigned based on business needs.

Additional Responsibilities

Education

Bachelor's Degree Mechanical, Biomedical or related Engineering field required

Work Experience

Minimum 3 years Related work experience required

Preferred Knowledge, Skills and Abilities

Background in medical device development or on-market sustainment
Knowledge of FDA medical device design controls (21 CFR 820.30)
Excellent communication skills including interactions with customers
Knowledge of statistics and Minitab
Project management skills
Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
Able to comply with the company’s safety and quality policies at all times

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.