Quality Assurance Specialist

Our client, a leading organization in the life sciences sector, is currently looking to add a Quality Documentation Specialist to their fast-paced quality team. This role will focus on document verification, production review, and quality system support to ensure compliance.

Responsibilities :

Perform detailed assessments and sign-off of completed manufacturing and packaging records for both individual components and final product assemblies.

Contribute to the resolution and documentation of quality-related issues, including support for deviational investigations and closure processes.

Assist with digital document management, including the upload of test protocols or assay-related materials (as needed).

Generate and assign batch identification numbers in line with internal tracking procedures.

Participate in the product labeling workflow by supporting label generation requests.

Digitize and archive completed records by scanning and organizing documentation for internal systems.

Requirements :

Associate’s degree in a scientific, technical, or communications discipline is preferred

Minimum of 1 year in a quality-related role, preferably involving documentation or manufacturing record reviews.

Exceptional accuracy and attention to detail are essential.

Familiarity with ERP platforms and digital record systems.

Effective communication skills, both written and verbal.

Strong organizational capabilities with the ability to manage multiple priorities.

Proven ability to work independently while collaborating effectively with cross-functional teams.