The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.
Lead the development, execution, and documentation of Analytical Method Validation (AMV) protocols and reports, ensuring analytical methods are accurate, precise, reliable, and compliant with applicable regulatory requirements. This includes methods used for the testing of raw materials, in-process samples, finished products, and stability studies.
Conduct cleaning validation analytical testing, periodic validation reviews, and laboratory equipment qualification activities to support the introduction and ongoing maintenance of laboratory systems and instruments.
Ensure the effective implementation, maintenance, and compliance of Computerized System Validation (CSV) requirements within the QC laboratory environment.
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Conduct routine analytical/microbiological testing of raw materials, packaging materials, finished products and environmental samples using approved methods and various instrumentation while adhering to cGMP and established policies.
Assist in analytical/microbiological method development, validation, revision and transfer including automated methods.
Interpret validity of own test data and generate accurate results.
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The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.
Act as quality liaison during the shift operation, ensuring GMP compliance in all areas of operation, including Production, Warehouse, QC Laboratory and Facilities area.
Advise teams on all aspects of GMP compliance and support the release of finished product release, assessing quality impact as necessary. Participate in on-line problems solving for quality issues, member of rapid response team in mitigating and resolving issues that arise during the shift.
Conduct regular process confirmation gemba, driving quality compliance and quality culture at site.
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Develops knowledge of functional area policies and procedures and performs routine analytical testing of sample functions.
Establish an understanding of requirements, laboratory processes and procedures, utilization of good documentation practices and other regulatory authority requirements.
Develops operational proficiency using analytical techniques and instrumentation to support sampling and testing for applicable products and incoming materials.
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