
Compliance and Regulatory Affairs Specialist
2 days ago
**Job Opportunity:**
The Compliance and Regulatory Affairs Specialist will be responsible for ensuring that all quality control activities in a medical device manufacturing facility comply with regulatory requirements. This role includes developing and implementing quality control procedures, monitoring adherence to quality standards, and investigating quality issues.
Responsibilities:
- Develop and implement quality control procedures to ensure compliance with regulatory requirements.
- Monitor adherence to quality standards, regulations, and best practices.
- Investigate quality issues or non-conformities and collaborate with other departments to resolve them.
Qualifications:
- Must have a pharmacy, biomedical engineering, or biotechnology degree recognized by HEC.
- A minimum of 5-6 years of experience in quality control and testing, preferably within a medical device manufacturing environment.
- Certification in quality control or quality management systems is preferred.
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