About the role
In this role, you will oversee quality assurance processes and ensure that all medical devices meet regulatory and quality standards. Your responsibilities will include reviewing production processes, conducting audits, and implementing corrective actions. This part-time position is ideal for experienced professionals looking to contribute to the quality of medical products.
The hiring company values integrity and quality, offering an environment where your expertise will be instrumental in enhancing product safety and efficacy. Join us in making a difference in healthcare quality.
What you'll do
- Conduct quality audits and inspections.
- Develop and implement quality control procedures.
- Ensure compliance with regulatory requirements.
- Train staff on quality assurance practices.
What you'll need
- Bachelor's degree in Engineering or Quality Assurance.
- 5+ years of experience in quality assurance in medical devices.
- Familiarity with ISO standards.
Skills
Strong analytical and problem-solving skills.
Excellent communication and interpersonal skills.
Knowledge of quality assurance methodologies.
Good to have
Experience with statistical analysis tools.
Knowledge of FDA regulations.
Benefits
- Competitive salary and flexible hours.
- Access to training and professional development.
- Collaborative work environment.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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Questions about this job
What are my main responsibilities in this role?
You will review production processes, conduct quality audits, and ensure compliance with industry standards.
What qualifications do I need?
A degree in engineering or quality assurance and 5-10 years of relevant experience is required.
Is this a full-time position?
This is a part-time role, providing flexibility in your schedule.
How can I apply for this job?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
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