Prepare SOPs for preventive maintenance of production machines and follow up its executionImplementation of preventive maintenance programsProvide prompt response to inquiries whenever there is a...

Analyze and monitor manufacturing costs, identifying variances and recommending corrective actions.Prepare detailed cost reports and present findings to management for informed...

Ensure compliance with GMP, GDP, and local regulatory requirements. Monitor implementation of Quality Management System (QMS).Review SOPs and ensure they are updated according to regulatory...

Review analysis raw data and COA.Analyzing finished products and their bulk samples.Able to perform on different lab instruments (Agilent and Shimadzu HPLC will be an advantage),Prepare different...

Execute Production related to R&D Department.Design, develop, and test new product formulations to meet customer requirements and market trends.Optimize existing product formulations to improve...

Writing the Analytical Reports and COA.Chemical and physical analysis according to method and specification after having the necessary training.Writing the Analytical Reports and COA.Preparation of...

Join our dynamic team in APEX Pharma, as a QA Data Integrity Professional! We're seeking a passionate and experienced Data Integrity Professional within our Pharmaceutical Quality Assurance...

Follow up annual regulatory plan executionReview regulatory documents and ensure they are up-to-date. Submission and follow-up new and reregistration process.Responsible for follow-up process at...

The formulation specialist will be responsible for designing, developing and optimizing pharmaceutical formulations for various products.Design, develop and test new product formulations to meet...

Review analysis raw data and COA.Analyzing finished products and their bulk samples.Able to perform on different lab instruments (Agilent and Shimadzu HPLC will be an advantage),Prepare different...

Analysis of R&D trials.Development of analytical procedure.Validation of the analytical procedure.Participate in the troubleshooting of the analysis problems in QC.Perform comparative dissolution...

Implementation and follow-up of the validation & qualification systems.Process validation.Cleaning validation.Review analytical method validation.Review calibration plans, follow their execution,...

Ensure following GMP roles in different production areas.Receive the weekly production schedule.Stick to the planned schedule and time table.Closely supervise different production processes and...

Responsible for archiving the documentation.Administrative tasks of the Approvals cycle.Manage, organize, and maintain all company documentation in accordance with established policies and regulatory...

Dealing with EDA inspectors and regulatory daily follow-up and activities.Responsible for document control and record control activities.Complete responsibility for the filing and archiving system...

Attend all the steps of manufacturing and packaging processes, sign in the batch record and perform all related in-process control testing.Checking machine/line for clearance and cleaning as per...

Responsible for archiving the documentation.Administrative tasks of the Approvals cycle.Manage, organize, and maintain all company documentation in accordance with established policies and regulatory...