Finished product QC Analyst At GSK
Job description
Are you looking for a new challenge to drive and improve quality control testing, with a chance to broaden your leadership skills? If so, this Finished Product & Stability Analyst role could be a great opportunity to consider.
As a Finished Product & Stability Analyst, you will be responsible for Testing and analyzing Lab. Samples, operate Lab. Equipment and instruments, and closely supervise the job carried out by Analytical/Stability analyst to ensure the quality of products and materials in compliance with GSK standard and specification, local requirements and GMP.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
Analyze and test bulk, finished products, stability samples and intermediates as well as finished products according to validated method of analysis and approved protocols and specifications.
Operate departmental section equipment and instruments according to approved SOP’s e.g. HPLC, GC, UV/Vis, IR and Atomic Absorption Spectrophotometer, balances and other analytical equipment.
Implement and maintain GMP, GLP and EHS requirements relevant to his/ her job.
Perform product validation analysis and cleaning validation analysis according to approved validation protocols.
Responsible for the stability stores and stability samples handling.
Prepare, standardize and maintain availability of reference standard, volumetric solutions, glassware, and reagents and ensure their good handling and storage according to the approved SOP’s.
Support GPS implementation in managing different activities relevant to the role.
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
Bachelor’s degree of pharmacy or Science.
Equipment manipulation and good computer skills.
(0 – 2) years practical experience in a pharmaceutical analysis preferably in multinational company. Fresh Graduates are welcomed.
Excellent command of English language.
Knowledge of GLP and GMP requirements.
Good communication and organization skills.