
Manufacturing Professional
3 days ago
Key Responsibilities:
- Review and validate engineering drawings for manufacturability, accuracy, and completeness as per the latest engineering standards.
- Apply knowledge of medical device regulations and execute gap assessments, manufacturing print reviews, and remediation activities.
- Participate in ideation activities to assess project scoping and viability through economic analysis, conflict analysis, and supplier quote validation.
- Conduct, review, and update models for tol-stackup studies and dimensional variation analysis (1D/2D) using Creo-CETOL or other tools.
- Apply project management skills to plan, schedule, and monitor project activities efficiently ensuring FTR & OTD excellence.
- Collaborate with global stakeholders across regions like category managers, sourcing, PM, and other cross-functional teams as per the project needs.
- Review and validate PPAP reports received from suppliers and assess if the technical specifications are met.
- Well-versed with Engineering Change Management procedures using PDM/PLM Software (Agile, Windchill, etc.).
- DFMEA/PFMEA and design reviews to assess and mitigate design & Mfg risks.
- Develop and refine detailed 2D drawings and 3D CAD models to support project requirements.
- Design Remediation (Engineering Specification Gap Assessment).
- Assist in developing Master Validation Plans, including process flow, OQ, and PQ.
- Perform CPK (Process Capability Index) and ANOVA (Analysis of Variance) studies.
- Conduct criticality analysis to ensure process reliability and quality.
- Bachelor's degree in mechanical/production engineering with Min 9–12 years of relevant experience.
- Strong expertise in DFM&A principles and manufacturing methods for plastics, metals, and packaging components & Systems.
- Proven experience in analyzing project feasibility for cost savings and efficiency improvements.
- Proficiency in CAD - Creo/SW and PLM/PDM tools (preferably Windchill).
- Solid understanding of project management methodologies, including planning, tracking, and cross-functional collaboration.
- Strong verbal & presentation skills for effective collaboration with global teams.
- Well-versed with MS PowerPoint, Excel for reports preparation, data analysis/advance operations.
- Proficient in conducting Production Part Approval Process (PPAP) to ensure compliance with technical specifications and quality standards.
- Skilled in performing detailed Root Cause Analysis to identify issues, implement corrective actions, and drive continuous improvement.
This role offers a unique opportunity to develop your skills in manufacturing engineering and contribute to the success of our organization.
">We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
">Others">Please note that this is a general job description and may be subject to change based on business needs.
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