Quality Assurance Role
We are seeking an experienced Quality Assurance professional to join our team. This is a fantastic opportunity for someone who is passionate about delivering high-quality results and working in a dynamic environment.
The successful candidate will be responsible for defining and implementing quality control techniques to ensure the quality of raw materials, intermediate, and end products. This includes managing and controlling all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.
The key responsibilities of this role include:
1. Organizing daily tasks to ensure efficient execution of sample analysis according to KPIs and laboratory schedules;
2. Maintaining adherence to GMP, HSE regulations, and industry standards in all analytical activities;
3. Ensuring accurate recording in checklists, laboratory records, and notebooks following GMP and internal procedures;
4. Performing routine equipment calibration and maintenance while ensuring hygienic lab conditions;
5. Reporting discrepancies, investigating atypical results, and supporting resolution of deviations and QC incidents;
6. Collaborating effectively with internal departments using relevant IT platforms for QC processes;
7. Assisting in audits and ensuring compliance with internal procedures under QC management guidance;
8. Seeking additional information when needed, completing self-assessments, and contributing to annual performance reviews;
9. Adhering to GMP, HSE, and legal regulations while maintaining high standards in laboratory operations;
10. Undertaking extra tasks as required and promoting safe, efficient laboratory practices.
To succeed in this role, you will need:
* A High School diploma (mandatory);
* Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (mandatory);
* Relevant work experience;
* Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (mandatory);
* Experience of GMP practices and HSE standards (preferable);
* Technical understanding of GMP practices, analytical theory and techniques - Clear and open communication skills (written and verbal);
* Competent (written and verbal) English language skills (preferable for sites where English is not the first language);
* Ability and availability to work in shift patterns, as required by business needs;
* Computer literate with knowledge of the MS Office package;
* Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down.
This is an exciting opportunity to join a leading organization in the pharmaceutical industry. If you are passionate about delivering high-quality results and working in a dynamic environment, please apply.