Job Purpose
In compliance with the Labor Code, the Public Health Code, Regulations, Good Manufacturing Practices, GSK Quality & EHS Standards and internal procedures:
Ensures physicochemical controls of materials raw materials, PSF, routine finished products, validation and stability, in compliance with regulatory and Quality requirements of GSK
(QMS, CAP).
Ensures the marketing of products compliant and of impeccable quality in compliance with GSK's regulatory and Quality requirements (QMS, CAP, pharmacopoeia).
Respect for costs, deadlines, quality, safety
Contribution to work of the team and the achievement of collective objectives.
Continuous improvement of his sector of activity.
Perform the tasks assigned to him by his Manager
Key Responsibilities
Execution of Analytical testing of all components, raw materials, excipient, intermediates, APIs, Final Product and ongoing stability samples.
Guarantee the reliability of the results obtained and identify any possible non-conformities and carry out the laboratory investigation.
Identifies CAPAs resulting from deviations, OOS, audits and ensures their implementation on time
Check and guarantee the reliability of the documents constituting and relating to the analytical control file.
Carry out analyzes according to schedule.
Maintains the working environment compatible with the activity (5S, storage, cleanliness, etc.) and ensures the proper use of laboratory material resources.
Ensures the management of reference standards, reagents, column, glassware and laboratory consumables.
Carries out L1 internal audits of its sector of activity and participates in the preparation of GSK internal audits (L3, L2 audit, and regulatory inspections and ensures the implementation of corrective & preventive actions on time.
Actively contributes to the introduction of new products on the site to meet the site's objectives by ensuring analytical transfers and analytical validation.
Conduct continuous improvement actions in your sector of activity, by integrating the laboratory's objectives (cost, quality, deadline, safety, environment, etc.)
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
Bachelor’s Degree Biology/Microbiology
2 or more years Experience as an analyst.
Proven experience working in teams to improve processes or resolve problems using organizational effectiveness tools.
Essential Skills and Abilities
If you have the following characteristics, it would be a plus:
Mastery of chromatographic control techniques.
Ability to synthesize and analyze.
Writing ability in French
Good command of English language reading and understanding
Application submission deadline 27/10/2023
Why Us?
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 organization 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.
Contact information:
You may apply for this position online by selecting the Apply now button.
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https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Laboratory-Analyst_382154
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