Production Operator | Basic RM 2000 - 2800 + OT Pay, Allowances, EPF, EIS, SOSCO

RecruitFirst; Seremban; On-site; MYR 20,000 - 100,000; Full time

Job summary

A manufacturing company is looking for a Production Operator to manage production processes, ensuring compliance with safety and quality guidelines. The ideal candidate should have 1 to 3 years of experience in a manufacturing environment and hold a Technical Certificate or Diploma in Pharmaceutical or Engineering. The role includes operating machinery, performing tests, and adjusting to production needs. Working hours are rotational shifts from Monday to Friday, with a competitive salary structure including basic pay and allowances.

Qualifications

• Minimum 1 to 3 years of experience in a manufacturing environment.
• Knowledge and experience in adhering to GMP and SOP guidelines in a production setting.

Responsibilities

• Operate and maintain production machine.
• Ensure production processes compliant with SOPs, GMP, and safety guidelines.
• Perform in-process tests, document records, troubleshoot issues, and meet production schedules.
• Assist with minor machine repairs and adapting to other production activities as required.

Education

Technical Cert or Diploma in Pharmaceutical / Engineering or equivalent

Job description

Position: Production Operator

Working Days: Monday to Friday

Working Hours (Rotational Shifts)

Day Shift: 8am to 8pm

Night Shift: 8pm to 8am

Middle Shift: 1.30pm to 1.30am

*Actual working hours may vary depending on operational shift rosters.

Salary

Basic Salary + Allowances + OT Pay + Statutory Contribution (EPF, EIS, SOSCO)

Responsibilities

Operate and maintain production machine.

Ensure production processes compliant with SOPs, GMP, and safety guidelines.

Perform in-process tests, document records, troubleshoot issues, and meet production schedules.

Assist with minor machine repairs and adapting to other production activities as required.

Requirements

Minimum 1 to 3 years of experience in a manufacturing environment.

Knowledge and experience in adhering to GMP and SOP guidelines in a production setting.

Qualification: Technical Cert or Diploma in Pharmaceutical / Engineering or equivalent.

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