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Automotive Team Leader at Sperton Malaysia

Subang Jaya City Council, Selangor, Malaysia -

Full Time

Start Date

Immediate

Expiry Date

17 May, 26

Salary

0.0

Posted On

16 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Tooling Coordination, T0 Trials, T1 Trials, T2 Trials, PPAP Documentation, Master Schedule Monitoring, Tooling Condition Verification, Drawing Verification, Packaging Design Modification, Abnormality Reporting, Recovery Plan, Countermeasures, QAV Support, SPTT Support, IATF16949 Preparation, 4M Change Documentation

Industry

Staffing and Recruiting

Description

Location : Bukit Raja Are you ready to lead new model launches from trial stage to mass production? If you have strong experience in tooling coordination, T0–T2 trials, and PPAP documentation — this is your chance to step into a high-impact leadership role. ⏰ Working Hours Day Shift Monday – Thursday: 8:00AM – 5:10PM Friday: 8:00AM – 5:20PM Night Shift Monday – Friday: 8:00PM – 5:00AM 💰 Salary: Attractive Package (TBC based on experience) Key Responsibilities Monitor and track Master Schedule with PIC Prepare & verify Tooling and CF condition upon receiving Conduct T0 readiness (tooling, drawing, semi glass, child parts) Manage T1 & T2 trial progress and draft reports Prepare lab test samples & robot teaching parts Handle packaging design modification & verification Manage abnormality reports, recovery plan & countermeasures Support QAV / SPTT / PPAP documentation Lead IATF16949 preparation activities Coordinate ECI / 4M change documentation We’re Looking For Someone Who: ⁠Must be Malaysian candidate Has experience in automotive manufacturing / new model projects ⁠Understands PPAP & IATF 16949 requirements ⁠Strong in reporting, coordination & problem-solving ⁠Detail-oriented and able to manage multiple tasks ⁠Comfortable working in day or night shift

Responsibilities

The Team Leader will be responsible for monitoring the Master Schedule and verifying tooling and component conditions upon receipt. Key duties include managing T1 and T2 trials, drafting reports, handling packaging modifications, and leading documentation efforts for QAV, SPTT, and PPAP.