GSKFull time Full day
Posted Date: May 24 2023
To ensure the testing related activities of Raw material, intermediate, finished product in compliance with QMS, cGMP and regulatory requirements.
Education & Experience
M.Sc. Chemistry or B-Pharm/ Pharm-D
Minimum 1 year of relevant experience
Perform testing of all SKUs according to IFS and TMs.
Be a team member of the level-1 Audit self-inspection.
Performing assigned laboratory duties.
Reporting of OOS/atypical results and a part of investigation team.
Registration of batch and test information in LIMS.
Analyst decision and analytical report generation of the assigned product.
Following EHS standards and guidelines in routine activities as per SOP.
Reporting EHS adverse events.
Maintain GMP in area.
Do daily calibration of Balances and pH meter and maintain record accordingly.
To follow GLP in the Laboratory.
Timely closure of QWF actions.
Worked as fire fighter of the department.
Preparation of reagents and mobile phase and maintain the records as per SOP.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.
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