Job Description:

Prepare all documents needed in process validation (protocols, sampling plan, reports…etc.). Reviewing, approving, and evaluating all documents generated in the process validation department (SOPs, protocols, reports…etc.). Monitor and execute the PV activities and collect the required samples. Follow up on the approval of all PV documents. Updating and reviewing PV history. Follow up plans and tasks on a daily basis. Coordinating, planning, and advising with related departments for process activities. Performing other duties related to the job as assigned by the direct supervisor/Manager Superb communication and interpersonal skills for coordinating between the various departments and staff of the company as well as the validation. Knowledge of the various state and federal pharmaceutical validation laws and legislations that are enforced from time to time. Must be well organized with good oral and written skills besides giving attention to details

 

 

Qualifications, Experience and Skills:

Bachelor Degree in Chemical Engineering or Pharmacist or relevant fields At least 0-3 years of experience in related fields