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 setting
Excellent communication skills for effective interaction with various stakeholders

Job Type: Full time

Perks
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