Quality Officer
CSH Pharma Group, Pakistan

Prepare, revise and maintain technical files and documents, SOP’s, Forms and Formats.

Collection and management of technical date from Quality, Production and other departments.

Assurance of proper security and confidentiality of documents generated also coordinate with IT department for storage of its Electronic documentation.

Coordinate with QA /QC Department for approval and revision control of technical files.

Follow up and update files, when required, to the latest version of product, material, or practices as per cGMP specifications.

Reviewing and archiving of production batch record, packaging and raw materials analysis records.

Maintains reference sample of each raw, packaging material and finished product.

Responsible for receiving finished product samples unit for MOH (Ministry of Health) & reference storage.

Responsible for following and compiling the products & materials release documentation from MOH.

Maintain filing of all master documents.

Any other task assigned by the supervisor.

Pharm D/ B. Pharmacy
Excellent written and verbal communication skills
Fully computer literate in (Word, Excel, Power Point, Outlook, Internet, etc)
Ability to organize and manage multiple task
Professional appearance
Strong organizational skills