Supplier Quality Auditor
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Job Location:
Monthly Salary:
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Are you passionate about ensuring the highest standards of quality and regulatory compliance in a dynamic environment Do you excel at building strong supplier relationships and driving continuous improvement If so we have an exciting opportunity for you to join our team as aSupplier Quality Auditor based in Brussels.
This is your chance to contribute to impactful work in the medical device industry where your expertise will directly support our mission of improving lives through innovation and quality.
As Supplier Quality Auditor you will be an integral part of our dynamic team. You will directly contribute to the success of our supplier auditing program by conducting audits to ensure suppliers meet strict regulatory and quality standards. Your work will play a vital role in maintaining the integrity and compliance of our supply chain.
What to Expect:
Conduct Supplier Audits:Execute audits (focusing on technical processes) to suppliers as part of the audit program ensuring compliance with applicable standards regulations and Hologic specifications. Review production processes to identify improvement opportunities.
Supplier Action Plan Management:Manage and follow up on supplier action plans (SACAs) resulting from audits and assessments.
Issue Escalation:Notify and escalate any potential supplier quality or regulatory issues to the Supplier Quality Auditing Manager that could impact product quality or compliance.
Cross-Functional Collaboration:Work with other Supplier Quality Auditors/Engineers and cross-functional teams to troubleshoot and resolve supplier quality issues. Identify Subject Matter Experts (SMEs) for audit teams as needed.
Reporting:Participate in reporting supplier quality Key Performance Indicators (KPIs).
Audit Documentation:Ensure supplier audit file records are accurate up-to-date and properly maintained.
Audit Scheduling:Participate on the development and maintenance of the annual audit/assessment program schedule using a risk-based approach including assessing controls and determining appropriate audit frequency.
Technical Expertise:Apply advanced knowledge of technical processes materials control and manufacturing processes to drive supplier quality improvements.
What We Expect:
Qualifications & Knowledge:
- Education:Bachelors degree in Engineering (Biochemical Chemical or related field). An ASQ Supplier Quality Engineer Certificate is a plus.
- Quality Auditor with an accreditation accreditation from one of the following: ASQ (American Society for Quality) CQA (Certified Quality Auditor) or CBA (Certified Biomedical Auditor) IRCA (International Register of Certificated Auditors) Lead Auditor Registration RABQSA Lead Auditor Certification or equivalent government body certification.
- Experiencewith master validation plans protocols and reports (IQ OQ PQ) and risk management (pFMEAs) process and documentation
- Industry Experience:7 years experience in medical device manufacturing or a related industry with 5 years in a Quality Auditing function preferred.
- Working knowledge ofMedical Device Regulations/In Vitro Diagnostic Regulation cGMP CFR 820 ISO-13485 (Required).
- Problem Solving:Proficiency with problem-solving tools such as SPC Total Quality Management and root cause analysis.
- Strong Communicator:Ability to effectively communicate at all levels of the organisation both written and verbal.
- Analytical Mindset:Skilled at analyzing data evaluating factors and translating insights into actionable plans.
- Self-Motivated:Able to work independently with minimal supervision while managing multiple complex projects.
Why Hologic
- Work on impactful projects that make a difference in the medical device industry.
- Build relationships with suppliers around the globe develop your skills and grow your career in a supportive and collaborative environment.
- Competitive salary and benefits package including health insurance
Travel Requirements:50%
Language Requirements:Proficient in English (written and oral). A second language is a plus.
#LI-HE1
Required Experience:
IC
Key Skills
- Quality Assurance
- Quality Inspection
- Calipers
- ISO 9001
- Quality Audits
- Process Mapping
- Fair Housing Regulations
- Quality Control
- Underwriting
- cGMP
- As9100
- Manufacturing
About Company
Hologic is a global champion of women’s health. We integrate The Science of Sure into everything we do to help improve and save lives through early detection and proactive treatment.
