Quality Assurance Expert

Job Description

Responsibilities:

Perform documentation and document control activities within the Quality Assurance (QA) department.

Prepare, review, register, and archive documents in accordance with company requirements.

Follow up on the preparation, revision, amendment, and distribution of documents.

Support the preparation and control of documentation required for product release processes.

Review the completeness and accuracy of product release documentation.

Follow up on required documents from relevant departments.

Maintain records and documentation in an organized manner.

Collaborate with Production, Quality Control, and Quality Assurance departments on documentation activities.

Prepare reports on documentation and process status.

Perform other assigned duties related to documentation and product release.

Qualifications:

At least 2 years of relevant experience in documentation, Quality Assurance, or product release within the pharmaceutical industry.

Bachelor’s degree in a relevant field.

Good knowledge of pharmaceutical documentation principles and processes.

Familiarity with GMP requirements and pharmaceutical documentation.

Familiarity with pharmaceutical product release processes and related documentation.

Good proficiency in Microsoft Office and Excel.

High attention to detail and accuracy.

Strong organizational, follow-up, and sense of responsibility.

Ability to work effectively in a team and coordinate with different departments.