Purpose of the Role:
To support the QA/QC Manager by ensuring timely batch release through review of batch documents, quality checks, sampling, and compliance with SOPs, GDP, and regulatory standards.
Key Responsibilities:
Perform physical and document-based batch release, including review of COAs/COS and quality certificates.
Conduct sampling, visual inspections, line clearance, and quality checks during packing and kit-packing activities.
Handle, investigate, and follow up on product deviations and supplier non-conformities.
Coordinate with suppliers for corrective actions and document closure.
Ensure proper use of data loggers during dispatch and compliance with GDP and ISO standards.
Maintain QA/QC documentation, SOPs, control samples, and eQMS records.
Act as quality contact for assigned customer segments and participate in quality-related meetings.
Competencies & Skills:
Good written and verbal English communication.
Detail-oriented, systematic, and proactive approach.
Working knowledge of MS Excel/Word and ERP systems.
Positive attitude and ability to manage routine quality tasks efficiently.

Keyskills: regulatory regulatory affairs medical equipment pharmaceuticals ra medical devices drug regulatory affairs
We’re an early-stage US startup building modern, scalable products to solve challenging real-world problems.