Mohd Bakhtiyar

Operations Associate

Gurgaon, Haryana, India12 yrs 10 mos experience

Most Likely To SwitchHighly Stable

Key Highlights

Over 10 years of experience in supplier quality management.
Certified ISO 13485:2016 Lead Auditor with extensive regulatory knowledge.
Proven track record in driving continuous improvement in healthcare supply chains.

Stackforce AI infers this person is a Supplier Quality Manager in the Healthcare industry, specializing in regulatory compliance and supplier performance.

Contact

Skills

Core Skills

Supplier Quality ManagementSupplier ManagementIso 13485New Product Development

Other Skills

ProcurementPerformance ManagementManufacturingSupplier QualitySupplier Quality EngineeringSupplier PerformanceAssociation ManagementLine ManagementSupplier AuditsMedical DevicesSupplier DevelopmentAPQPPPAPKaizen8D Problem Solving

About

Supplier Quality Manager | ISO 13485:2016 Lead Auditor | 10+ Years of Experience I am a results-driven quality professional with over a decade of experience managing supplier quality teams and ensuring compliance in the medical device industry. My background includes extensive work with both OEMs and Contract Manufacturers (CMs), ensuring products meet the highest standards of safety, quality, and regulatory compliance. 🎯 Key Certifications: ISO 13485:2016 Lead Auditor – Certified by BSI, a globally recognized authority APQP/NPIP Engineer – Also certified by BSI 🧩 Core Competencies: Supplier Quality Management & Audits APQP, PPAP, 8D, and CAPA Nonconformance (NC) investigations and resolution Medical device regulatory compliance and documentation control I am passionate about building robust supplier partnerships and driving continuous improvement to meet the stringent demands of global healthcare markets.

Experience

12 yrs 10 mos

Total Experience

6 yrs 5 mos

Average Tenure

7 yrs 3 mos

Current Experience

Stryker

4 roles

Associate Manager, Global Supplier Engineering

Mar 2026 – Present · 2 mos

ProcurementPerformance ManagementManufacturingSupplier ManagementSupplier QualitySupplier Quality Engineering+4

Team Lead, Global Supplier Engineering

Sep 2024 – Mar 2026 · 1 yr 6 mos

Staff Quality Engineer

Mar 2023 – Sep 2024 · 1 yr 6 mos

Supplier QualitySupplier PerformanceSupplier Quality EngineeringSupplier AuditsMedical DevicesSupplier Management+2

Sr. Engineer Quality Assurance

Feb 2019 – Mar 2023 · 4 yrs 1 mo

Handling OEM/CM suppliers for Stryker European Buying Center (EBC).
Handling Supplier Initiated Change Request of OEM/CM suppliers as per the required deliverable.
Review of technical documentation from supplier for any change control.
Leading Complaints communication between suppliers and Division for complaint overview and find out the best possible way to resolve the issues.
Working on Supplier Incidents initiated by warehouse and take appropriate actions by opening NC in TrackWise.
Handling NC/CAPA and responsible for all the Quality related issues for supplier.
Responsible for supplier Corrective and preventive Action with effective monitoring for successful CAPA.
Lead the NC/CAPA process and Employee Onboarding Workstream through generating new templates for effective utilization of communication and achieved the Metrics/Goals.
Involvement in various improvements like SICR corporate procedure, Supplier Certification, EBC MDI calls.
Support Division for any queries related to the supplier.

Rakheja engineers pvt ltd

Assistant Manager

Jul 2013 – Feb 2019 · 5 yrs 7 mos · Faridabad, Haryana, India

Responsible for Supplier Quality, New Product Development, Supplier Development & upgradation.
Analyzing In-house & Incoming rejection. Publish supplier Ratings quarterly as well as Annually.
Good experience in Heavy Fabrication (MIG Welding), Machining, Casting, Forging & Powder Coating process.
Maintaining of all documents like PPAP, calibration, validation, APQP document at supplier end.
Conducted APQP process to achieve PPAP for designated supplier in support of new product launches.
Reduced RPN through Kaizen and Poke-yoke.
Monitor day to day shop floor activities, rejections at supplier end, Incoming Inspection and development parts and initiate necessary corrective actions
Participating in Problem discussion at In-house
Prepare PPAP documents – Process flow Diagram (PFD), Failure Mode & Effect Analysis (FMEA), Control Plan (CP).
Conducted effective analysis of failure or issues to determine root cause and implement corrective action best suited for implement
Identification of scope of improvements in Tooling/fixtures, gauges & getting them implemented.
Lead continuous improvement through regularly scheduled supplier assessments and closed loop 8D supplier corrective action system.
Responsible for new project. (NPD Quality planning to new part approval from customer).
Maintaining supplier audit, internal audit and NC Record.
Supervision of Incoming Inspector – Incoming Inspection reports, BOP Validation, Review CAPA for Non Conformance part
Conduct Supplier Process Audit & Supplier performance Ratings.
Knowledge of CMM programing software CAM2 Measure 10.4 (FARO Arm)Lead continuous improvement through regularly scheduled supplier assessments and closed loop 8D supplier corrective action system