Are you a detail-oriented and passionate engineer ready to kick-start your career in supplier quality? We are seeking a dynamic Supplier Quality Engineer to join our innovative team onsite in Newark, DE, supporting our Breast and Skeletal Health Division. This is an exciting opportunity to work closely with suppliers, ensure the highest quality standards, and make a significant impact on women's health.

 

What You'll Do:

Supplier Quality Management: Collaborate with global suppliers to ensure compliance with quality standards and specifications. Conduct supplier audits and assessments to identify areas for improvement and ensure adherence to requirements. Quality Assurance: Perform inspections and evaluations of incoming materials, components, and services. Assist in the development and implementation of quality control procedures and processes to maintain high standards. Technical Support: Provide technical knowledge and expertise across the organization to ensure suppliers meet all requirements. Support the Global Supplier Quality organization dedicated to the oversight of components, materials, and services. Problem-Solving and Analysis: Investigate and resolve supplier-related quality issues promptly. Conduct root cause analysis and implement corrective and preventive actions (CAPAs) to prevent recurrence. Documentation and Reporting: Maintain accurate records of supplier performance and quality metrics. Prepare detailed reports and documentation for internal and external stakeholders to ensure transparency and accountability. Cross-Functional Collaboration: Work closely with the Breast and Skeletal Health Division to support quality initiatives and drive continuous improvement. Participate in cross-functional teams to foster innovation and enhance supplier quality.

Why You'll Love It Here:

Impactful Work: Play a crucial role in ensuring the quality of products that enhance women's health and well-being globally. Professional Growth: Gain hands-on experience and develop your skills in supplier quality management and technical support. Collaborative Environment: Be part of a supportive and forward-thinking team that values innovation and excellence. Onsite Experience: Work directly with our team in Newark, DE, and make a tangible impact on our operations and supplier quality.

 

If you are ready to take on a rewarding role that allows you to drive supplier quality and support groundbreaking healthcare solutions, apply today and become an integral part of our mission to enhance women's health!

 

Qualifications: 

Education and Experience 

Bachelor’s degree (BA or BS) from a university in Electronics or Mechanical Engineering or related Engineering field. ASQ      Supplier Quality Engineer Certificate a plus. Specialized Knowledge (Desirable): Medical device regulations (21CFR), ISO 13485, ISO 9001, Medical Device Single Audit Program, and other international regulations. Knowledge of automotive APQP process is a plus.

 

Experience   

No experience required. Desirable if the candidate has done an Internship in the Medical Devices industry or in a regulated environment related. 

 

 

Skills

Communication—must be able to effectively communicate in both written and verbal forms, and at all levels in the organization. Knowledge of project management techniques. Ability to use problem-solving tools (SPC, TQM, etc.) to optimize processes. Ability to analyze a situation or data; evaluate relevant identifiable factors and translate this information into a meaningful proposal or action plan. Ability to effectively communicate ideas and approaches in the form of proposals, plans and presentations. High proficiency with Microsoft Office suite to produce reports, analyze data, etc. effectively.  Ability to handle and manage multiple complex projects.  ISO 13485 leader auditor (Desirable). Quality System Regulation (Desirable). Negotiation course (Desirable). Risk management (Desirable).  Validations and root cause analysis (Desirable). PPAP (Desirable). Proficiency with Agile and Oracle (Desirable).  Must follow all applicable FDA regulations.  Computer tools and knowledge: Microsoft: Intermediate to advanced: Internet: yes; email: yes. Language: Proficiency written and oral in English. A second language is a plus. 

 

 

So why join Hologic?

 

We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and annual bonus scheme, one of our talent partners can discuss this in more detail with you.

 

If you have the right skills and experience and want to join our team, apply today. We can’t wait to hear from you!

 

 

The annualized base salary range for this role is $62,900 - $98,400 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.

 

Agency and Third-Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

 

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

 

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