Final Quality Control (FQC):
Inspect finished products before release.
Conduct functional/electrical tests, visual inspections, and packaging checks.
Review Device History Records (DHR) to confirm compliance with design and regulatory requirements.
Maintain detailed records of inspections, TEST results, and quality control reports.
Document control:
Assist with the issuance, revision, and archiving of controlled s, such as procedures, work instructions, forms, and records.
Maintain logs and ensure proper version control.
Ensure obsolete s are removed and replaced as needed.
Support the document review and approval workflow, including tracking pending approvals.
File and maintain both electronic and paper documentation in an organized manner.
Requirements: Education:
Certification in Quality Control Advantage.
Language Skills:
Proficient reading comprehension in English required
Experience:
Experience in industries such as medical devices, pharmaceuticals, or electronics.
Proven experience in quality control or Quality Assurance.
Experience with Quality Management Systems (QMS), Statistical Process Control (SPC), and other quality methodologies.
Technical Skills:
Familiarity with and proficiency in inspection equipment, such as calipers, micrometers, and microscopes.
Knowledge of industry standards such as ISO 9001, ISO 13485, or similar quality certifications
Highly organized with excellent attention to detail
This position is open to all candidates.