The Summer Internship Experience: Make a Difference
As a Hologic Intern, you are not just taking a summer job; you are taking your place on a global team of motivated, creative and amazing people! The summer internship experience gives you the opportunity to shine and share your knowledge, energy, and passion on meaningful projects that impact people all over the world. In addition to a project that will provide maximum experience and exposure in your desired field the Hologic College Relations team provides opportunities to learn more about the company, network with leadership, and develop the skills needed to succeed in a global organization.
The Design Assurance team ensures that safety and effectiveness are design into, and maintained, for our products. The Design Assurance role is responsible to facilitate the application of design controls while supporting new product development activities and manufacturing related design changes with a key focus on quality system compliance, risk management leadership and change analysis.
The Design Assurance intern will be responsible for the following:
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Updating the Danbury QMS Verification and Validation protocol templates to the current best practices; Update verification and validation report templates to help standardize report generation for V&V. If time permits, additional template updates might be explored.
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Work closely with R&D and V&V team members to help understand the needs of those who will be generating the protocols and reports.
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Placed on an active project development team alongside their mentor to get "hands-on" experience on providing DA support. The intern will be assigned actions to support the project with the guidance of the mentor.
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The intern will learn about design controls, regulatory standards, traceability, and Risk Management.
We’re looking for bright, inquisitive problem solvers who strive to make a difference. In order to be considered for this internship you must:
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Be enrolled as a Rising Junior or Graduate MBA
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Majoring in: Biomedical Engineering or related major
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Have a 3.2/4.0 GPA
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Familiarity with FDA Quality System Regulations, especially Design Control requirements, ISO 13485, ISO 14971 and EU Medical Device Regulation.
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Ability to appropriately assess written documentation as an advocate for compliance and ability to effectively communicate assessment.
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Microsoft Office (Word, Excel, Outlook, Power Point)
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Effective written and oral communication skills, with a focus in technical content.
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Ability to effectively work in dynamic team environments.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.