
Chief Compliance Officer
1 week ago
We are seeking an experienced Senior Quality Assurance (QA) Analyst to join our Quality team and support our compliance-driven growth.
- Key Responsibilities:
- Ensure adherence to product and process quality standards in medical device manufacturing
- Participate in internal audits and support external regulatory inspections (DRAP, ISO, etc.)
- Maintain and manage compliance documentation, including SOPs and quality records
- Support improvements to QA systems and drive a culture of continuous compliance
- Collaborate with cross-functional teams on CAPAs, validations, and change controls
Requirements
- Education: Pharm-D or degree in a science-related field
- Experience: 3–4 years in QA, preferably in the medical device or healthcare manufacturing sector
- Strong knowledge of ISO 13485, GMP, and regulatory documentation practices
- Excellent attention to detail, organizational, and communication skills
- Ability to work independently and collaboratively in a regulated environment
Benefits of this role: The successful candidate will have the opportunity to make a significant impact on the quality and safety of our medical devices. In return, we offer a competitive salary, a dynamic and supportive work environment, and opportunities for professional growth and development.
About the job: As a Senior Quality Assurance Analyst, you will be responsible for ensuring that our products meet the highest standards of quality and safety. You will work closely with cross-functional teams to identify and implement process improvements, maintain compliance documentation, and support external regulatory inspections.
How to apply: If you are a motivated and detail-oriented individual with a passion for quality assurance, please submit your application. We look forward to hearing from you
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