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Finished Goods Laboratory Team Lead

Job in Cape Town, 7100, South Africa
Listing for: Haleon
Full Time position
Listed on 2026-01-25
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, QA Specialist / Manager, Quality Control / Manager, Quality Technician/ Inspector
Job Description & How to Apply Below
Finished Goods Laboratory Team Lead page is loaded## Finished Goods Laboratory Team Lead locations:
South Africa - Western Cape - Cape Towntime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
February 7, 2026 (14 days left to apply) job requisition :
539548

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.
Our trusted portfolio of brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.
Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.
** About the role
*** Manage and lead the analytical activities related to testing of Finished product and stability program and NPI Validation Program.
* Support the Quality Control Manager to define department goals in line with Site/QA goals & prioritizes work accordingly.
** Key responsibilities
*** Manage testing and release of Bulk and Finished Products ensuring compliance with quality standards.
* Supervise analytical activities and ensure adequate resources and adherence to testing plans.
* Implement robust processes for assessing and approving test results.
* Ensure OOS process is implemented and followed, and that laboratory non-conformances or deviations are effectively investigated and documented within the mandated timelines
* Establish and lead Stability program per local regulatory guidelines and applicable standards.
* Manage sampling, testing, and documentation as per protocol.
* Communicate stability issues impacting product quality promptly.
* Develop and validate analytical methods to ensure suitability.
* Manage method validation protocols, data, and reports.
* Monitor and review validated methods for ongoing effectiveness.
* Ensure QC operations comply with internal and regulatory standards.
* Implement HQS procedures.
* Conduct training on analytical methods and procedures.
* Ensure that Data Integrity (DI) and ALCOA principles and guidelines are followed in line with the required policies and procedures.
* Ensures that QC staff are adequately trained and developed to ensure that they are multiskilled to support areas within remit and outside (e.g. Incoming Materials testing).
* Ensures laboratory compliance with Inspection Readiness elements relevant to the area.
* Maintain Good Laboratory Practice standards.
* Ensure compliance with EHS standards and policies.
* Ensure compliance to the EHS and Engineering Improvement plans.
* Manage Lab. EHS risk assessment, control and governance and safety incidents reporting.
* Identify and address EHS training needs.
* Manage QC Lab personnel, including recruitment and training.
* Conduct performance appraisals and manage HR administration tasks.
* Provide input into QA budget and capital expenditures.
* Drive operational efficiency and quality lab. Improvements through e.g., testing optimization,  lab cycle time improvement, automation…etc.).
* Monitor performance metrics and lead continuous improvement initiatives.
* Ensure Gemba actions are documented and tracked in the area.
** Qualifications and skills
**** Essential
* ** Diploma in Chemistry or equivalent Scientific discipline
* Minimum 5 years in the pharmaceutical or consumer industry with preferable operational and Quality experience.
* Knowledge of Quality Assurance Systems and cGMPs.
* Understanding of working in a highly regulated and fast paced environment
** Preferred
* ** Degree in Chemistry or equivalent Scientific discipline
* Analytical or Industrial Chemistry
* People management experience
** Skills
* ** Holds high ethical standards.
* Strong commitment to EHS and knowledge…
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