Job Description You will be calling on doctors to promote and sell our ethical products. Besides this, you will conduct sales presentation of our ethical
Job summary Assist senior in executing validation and qualification activitiesSupport technology transfer and scale up activitiesProvide technical assistance
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 / Line Leader within the respective section. 2. To be responsible in delivering
**Job Outline**: 1. To operate machine / work activities upon instructions within the respective section. 2. To assist 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
Job summary Compliance with GLP and cGMP Setting up equipment for tests and trials Performing maintenance and troubleshooting Job seniority:associate level
Job summary Work closely with key stakeholders to ensure smooth and efficient stock supply Responsible for monitoring inventory in depots throughout Malaysia
Job Outline: 1. To provide high-level clerical support to senior executives at a company or organization. 2. To co-lead and guide the Administrative Officer
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 / Line Leader within the respective section. 2. To be responsible in delivering
**Job Outline**: 1. To operate machine / work activities upon instructions within the respective section. 2. To assist 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