Job Description

Requirements:

Degree in Chemistry, Chemical Engineering or Biology OR Graduate in any Science dicipline. Minimum 1 year working experience in Pharmaceutical industry. Highly on social responsibility, indicating desire fair outcomes and have a general concern for others. Tend to be high on the measure of conscientiousness, methodical, reliable and generally plan out things in advance. Excellent verbal & written communication skills, knowledge of quality standard, able to work in team and attention to details.

Job Summary:

Primary role is to govern Process Validation (NPD) and establish routine validation plan (schedule, coordinate, monitor and execute validation activities) which consist of initiating protocol and report, monitor, coordinate and execute validation activities as per Validation Master Plan Schedule to ensure GMP compliance and continuous improvement.

Key Accountabilities:

Report to Head of TS directly on any matters related to validation and selected functions. To involve directly in planning and execution of any qualification and validation activities associated with Validation Master Plan (VMP). To prepare and maintain all relevant protocols and report regarding any qualification and validation activities associated with Validation Master Plan (VMP). To govern the Analytical Method Validation (AMV) activities through reviewal of the documents. Conduct data analysis, compile test report and prepare validation report to summarize overall outcome, conclusion and recommendation. Conduct risk analysis involving process, product or equipment to be validated or qualified prior to identify CPP, CQA and worst-case conditions. Assist Head of TS in GMP audit closure and ensure relevant actions have been taken and effective. To apply problem solving tool or statistical tool in handling quality issues and ensure root cause is identified and resolved if it is detected throughout the validation activities. Assist HRS to compile all the relevant dossier document for regulation submission. Coordinate validation committee meeting and participate in GMP related activity such as audit, training, and Quality Risk Management. To support and perform other TS Sr Executive/Executive duties when he/ she is absent or out of office. To adhere to company policies and work as a team in achieving company objectives. To carry out any other task assigned by Head of TS and Deputy Director of Quality Assurance.
Job Types: Full-time, Permanent

Pay: RM2,400.00 - RM3,500.00 per month

Benefits:

Additional leave Dental insurance Flexible schedule Free parking Health insurance Maternity leave Meal allowance Opportunities for promotion Professional development Vision insurance Work from home
Ability to commute/relocate:

Rawang (48020): Reliably commute or planning to relocate before starting work (Required)
Application Question(s):

Do you have experience working in pharmaceutical industries? Yes or No
Education:

Bachelor's (Required)
Experience:

Technical Service: 1 year (Required)
Work Location: In person