Quality Management Systems Specialist

About the role

The Quality Management Systems Specialist will lead quality assurance activities for CooperVision's Victor site, supporting new product launches, packaging, documentation, and validations. This full‑time onsite position ensures compliance with global quality processes and regulatory standards.

Key responsibilities

• Conduct QA reviews of 4,000+ quality records annually, handling discrepancies, non‑conformances, and investigations.
• Lead cross‑functional teams on change orders, problem reports, CAPA/NCR processes, and internal audits.
• Maintain and update SOPs, work instructions, and controlled documents using the electronic QMS (eQMS).
• Provide training on QMS and Good Manufacturing Practices (GMP) to site personnel.

Required profile

• 2‑3 years of Quality Assurance experience, preferably in the medical device industry.
• Strong analytical, problem‑solving, and communication skills.
• Ability to work independently and prioritize tasks in a fast‑paced environment.

Required skills

• Microsoft Office Suite (Excel, Access)
• Experience with Agile methodologies
• Proficiency in electronic Quality Management Systems (eQMS)
• Knowledge of GMP regulations and ISO quality standards