Project Engineer - Quality

Role overview

This opportunity is for a Project Engineer in Quality with a US-based product company operating from Gurugram. The position is based in Phase-1 of the IT/ITES SEZ at International Techpark (ITPG), Gurgaon. The employer is looking for someone with 2 to 6 years of experience, and the expected joining time is immediate to a maximum of 30 days.

Key responsibilities

• Drive improvements in the company’s and suppliers’ change-request workflows, especially around Supplier Initiated Change Requests (SICRs).
• Take ownership of the electronic platforms used for SICR processing and keep the related data accurate and aligned across systems such as the SICR database and OnePLM SICR library.
• Check supplier-submitted SICR forms for missing details or inaccuracies and work with suppliers to correct them so the change can move forward smoothly.
• Manage SICRs raised by global suppliers end to end.
• Assess submitted change requests, identify gaps in the supporting information and required deliverables, and ensure readiness for approval.
• Arrange SCRB discussions with key stakeholders and secure agreement on the appropriate type of change.
• Review supplier deliverables, approve the ones that meet expectations, and coordinate revisions when corrections are needed.
• Process ECRs, ECNs, and promotion requests in OnePLM to support change approval activities.
• Support internal and external communication channels involving suppliers, sites, and divisions.
• Track and maintain SICR performance metrics and KPIs.
• Contribute to global SICR improvement initiatives.
• Work confidently with WINDCHILL, OnePLM or similar change-control tools, SAP or similar ERP systems, and design control systems.
• Apply technical knowledge of GD&T, PPAP, APQP, PFMEA, DFMEA, CQA, validations, and design change-control practices.

Requirements

• A bachelor’s degree with honors in Engineering, Science, or an equivalent qualification is required.
• At least 3 years of experience in a manufacturing environment or a similar setup is expected.
• Basic familiarity with GMP, ISO 13485, and 21 CFR Part 820 standards is needed.
• Strong communication skills are essential.
• Sound understanding of continuous improvement practices is required.
• Hands-on experience preparing, reviewing, and getting supplier approval for PPAP, MSA, and SPC documentation is necessary.
• Practical exposure to validation activities such as IQ, OQ, and PQ is required.
• Experience with PFMEA and Control Plan development and maintenance is expected.
• Applicants should be comfortable working in a team setting and collaborating across functions.
• The role calls for a highly motivated professional who can build strong internal and external relationships.
• Multitasking ability is important, as the position involves handling several priorities at once.
• The ideal candidate should enjoy a fast-paced, results-driven environment focused on quality, compliance, and customer satisfaction.

Eligibility

Any graduate can apply, provided they also meet the experience and skill requirements described for the role.

Additional details

Applicants should have 2 to 6 years of overall experience. The hiring team asks candidates to include the following in their response: total experience, relevant experience in Quality Management, PPAP, APQP, MSA, NPD, Change Management, and Control Plan, relevant experience in the medical device industry, current CTC, expected CTC, official notice period, willingness to work from the IT/ITES SEZ in International Techpark (ITPG), Gurgaon, and availability for MS Teams as well as face-to-face interviews on weekdays.

The notice period requirement is immediate joining up to a maximum of 30 days. Candidates should not alter the subject line when replying. The job is based in Gurugram and is intended for candidates who are ready to work from the specified location.

How to respond

Interested candidates were asked to share an updated profile by email for consideration.