Job Summary The Quality Assurance Associate/Document controller will be responsible for ensuring that products meet the established standards of quality, reliability, and performance through various inspection and testing processes. And also responsible for the company`s eQMS system_Veeva Vault/C15

Duties

- Managing and maintaining all controlled company documents: This involves ensuring that all documents are up-to-date and compliant with GMP regulations.

- Updating and controlling procedure documents and forms: This includes creating, revising, and maintaining company standard operating procedures (SOPs) as required.

- Preparing correspondence, bills, statements, receipts, checks, or other documents: This ensures that all necessary documentation is prepared and submitted as needed.

- Copying information from one record to another: This involves ensuring accuracy and consistency across all documents.

- Compiling records and reports: This includes preparing and maintaining records that are essential for audits and investigations.





- These duties are crucial for ensuring the integrity of the company's documentation and supporting regulatory compliance. The document controller plays a vital role in maintaining a compliant and efficient document control system within the GMP environment.

Requirements

- Previous experience in document control is an asset

- Proficiency in analyzing data and identifying trends/ microsoft office

- Strong attention to detail and accuracy in work

- Knowledge of quality inspection techniques and procedures

- Familiarity with quality assurance principles and practices

- Ability to work collaboratively in a team environment

- Excellent communication skills for effective interaction with various stakeholders

Job Type: Full time

Benefits

- Company pension

- Dental care

- Extended health care

- Life insurance

- On-site parking

Education

- Secondary School (preferred)

Work Location: In person

📌 Document Controller (Cremona)
🏢 CannaPharmaRX
📍 Cremona