The order in which job vacancies are displayed is determined by a composite score based on the following factors:
Keyword Relevance: How well your search terms match the vacancy details. We prioritize matches found in the job title, followed by job requirements, location names, and educational levels. Matches within general employer information or the organization's name carry a lower weight.
Commercial Prioritization (Premium Jobs): Vacancies paid for by employers ('Premium' or 'Sponsored') receive a ranking boost and will appear higher in the search results.
Recency (Date Relevance): Newer vacancies are prioritized. The relevance score of a vacancy is reduced by half once the posting is older than 30 days.
Proximity (Distance Relevance): Vacancies located closer to your search location are ranked higher. For vacancies located more than 30 km from the search center, the relevance score is halved.
The final ranking is established by multiplying all these individual factors to calculate the total relevance score.
Accountable for improving quality, compliance and embracing good quality culture within the laboratories. Working with commitment with the Pharmaceutical Quality System that is in place by following procedures and always maintaining the integrity of all laboratory data.
* To be responsible for the raw material/Finished Product and packaging components booking in sampling and testing process.
* To test and report results to GMP standards as per company SOP's.
* To perform routine physical testing as per approved methods.
* To calibrate and maintain equipment in the laboratories.
* To troubleshoot routine laboratory issues when they arise.
* To operate standard laboratory instruments including HPLC, GC, Auto titrator, UV spectrometer and Dissolution apparatus.
* To maintain laboratories to GMP standards.
* To routinely test raw materials, finished product, stability samples and investigational samples using analytical techniques.
* Sample booking in and collection for routine analysis.
* Managing FP team consumables needs.
* Support, engage with and implement continuous improvement projects in QC department and collaborate with other departments for site projects.
* Adherence to laboratory compliance with internal, external and regulatory requirements for Quality Control Finished Product/Raw Material testing.
* Any other duties as required.
ESSENTIAL EXPERIENCE, SKILLS AND ABILITIES
* Relevant degree in a scientific discipline.
* A good understanding of GMP.
* Excellent time management and organization skills.
* Cost conscious.
* Excellent verbal and written communication skills.
* Experience working in a laboratory environment for 1-2 years is desirable.
* Proficient in the use of Microsoft Office including Word and Excel.
* Passion for Continuous Improvement.
* Sets and resets priorities to remain focused on objectives in rapidly changing circumstances.
* Basic understanding of statistics and its application to experimental work