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
Scanning of documents Require to stand in a period of time for scanning activity. Good in computer skill will be added an advantage.Founded in 1967 in
At least 1 year of experience in process Quality Control in any related field. Strong in analytical / mathematic Able to work in shift and extra time Good
Job Outline: 1. To supervise a team of Process Assistant / Technologist within the respective section. 2. To be responsible in delivering production output in
**Responsibilities**:- Has experience in QC chemical testing for at least 1 year**Benefits**:- EPF- SOCSO- Annual Leave
**Responsibilities**:- Has experience in QC / QA documentation for at least 1 year**Benefits**:- EPF- SOCSO- Annual Leave
To perform routine activities of planning, transferring and receiving of goods in warehouse with high level of productivity by ensuring compliance with all
Job Outline: You will be responsible for the sales of the Company's products to pharmacies in your assigned territory. You will develop and establish sales
Job Outline: As part of a fast-growing team, the selected incumbent will be responsible for developing, designing and executing marketing plans and strategies
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
At least 1 year of experience in process Quality Control in any related field. Strong in analytical / mathematic Able to work in shift and extra time Good
Scanning of documents Require to stand in a period of time for scanning activity. Good in computer skill will be added an advantage.Founded in 1967 in
Job Outline: 1. To supervise a team of Process Assistant / Technologist within the respective section. 2. To be responsible in delivering production output in
**Job Outline**:1. To carry out work activities upon instructions within the respective section to manufacture pharmaceutical products in compliance with cGMP
**Responsibilities**:- Has experience in QC chemical testing for at least 1 year**Benefits**:- EPF- SOCSO- Annual Leave
**Responsibilities**:- Has experience in QC / QA documentation for at least 1 year**Benefits**:- EPF- SOCSO- Annual Leave
To perform routine activities of planning, transferring and receiving of goods in warehouse with high level of productivity by ensuring compliance with all
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
At least 1 year of experience in process Quality Control in any related field. Strong in analytical / mathematic Able to work in shift and extra time Good
Scanning of documents Require to stand in a period of time for scanning activity. Good in computer skill will be added an advantage.Founded in 1967 in