Job summary Compliance with GLP and cGMPSetting up equipment for tests and trialsPerforming maintenance and troubleshooting Job seniority: associate level
1. To ensure compliance to safety rules, Good Laboratory Practices, MS ISO/IEC 17025, ISO9001, ISO13485, EU GMP, PICs/GMP and other applicable Standards in
Attend breakdowns, identify fault and problem solve with mínimal downtime to production.Repair faulty equipment units.Plan and schedule repairs.Conduct
**Duties/Responsibilities**:- Attend breakdowns, identify fault and problem solve with mínimal downtime to production.- Repair faulty equipment units.- Plan
1. To ensure compliance to safety rules, Good Laboratory Practices, MS ISO/IEC 17025, ISO9001, ISO13485, EU GMP, PICs/GMP and other applicable Standards in
**Job Outline**:1. To carry out work activities upon instructions within the respective section to manufacture pharmaceutical products in compliance with cGMP
Attend breakdowns, identify fault and problem solve with mínimal downtime to production.Repair faulty equipment units.Plan and schedule repairs.Conduct
**Duties/Responsibilities**:- Attend breakdowns, identify fault and problem solve with mínimal downtime to production.- Repair faulty equipment units.- Plan
SALES REPRESENTATIVE ( MEDICAL PRODUCT SPECIALIST ) Melaka Pharmaceuticals & Medical Devices (Healthcare & Medical) SALES REPRESENTATIVE (MEDICAL PRODUCT
1. To ensure compliance to safety rules, Good Laboratory Practices, MS ISO/IEC 17025, ISO9001, ISO13485, EU GMP, PICs/GMP and other applicable Standards in
Job Outline: 1. To supervise a team of Process Assistant / Technologist / Line Leader within the respective section. 2. To be responsible in delivering
**Job Outline**: 1. To carry out work activities upon instructions within the respective section to manufacture pharmaceutical products in compliance with cGMP
Attend breakdowns, identify fault and problem solve with mínimal downtime to production. Repair faulty equipment units. Plan and schedule repairs. Conduct
Job summary Compliance with GLP and cGMP Setting up equipment for tests and trials Performing maintenance and troubleshooting Job seniority:associate level
1. To ensure compliance to safety rules, Good Laboratory Practices, MS ISO/IEC 17025, ISO9001, ISO13485, EU GMP, PICs/GMP and other applicable Standards in
Job Outline: 1. To supervise a team of Process Assistant / Technologist / Line Leader within the respective section. 2. To be responsible in delivering
**Job Outline**: 1. To carry out work activities upon instructions within the respective section to manufacture pharmaceutical products in compliance with cGMP
Attend breakdowns, identify fault and problem solve with mínimal downtime to production. Repair faulty equipment units. Plan and schedule repairs. Conduct
**Duties/Responsibilities**: - Attend breakdowns, identify fault and problem solve with mínimal downtime to production. - Repair faulty equipment units. -
1. To ensure compliance to safety rules, Good Laboratory Practices, MS ISO/IEC 17025, ISO9001, ISO13485, EU GMP, PICs/GMP and other applicable Standards in