Quality Assurance Intern

Advita Ortho

Gainesville (FL)

On-site

USD 20,000 - 35,000

Part time

14 days+

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Job summary

Advita Ortho is looking for a Quality Assurance Intern in Gainesville, FL, to assist the QA Engineering team with various projects aimed at enhancing an efficient Quality program.

The ideal candidate is pursuing a bachelor’s or master’s degree in Mechanical Engineering, Biomedical Engineering, or Materials Science. Responsibilities include supporting post-market complaint investigations, inspection planning, and the creation of Quality Management System documentation.

Qualifications

  • Currently enrolled in Junior or Senior year of Bachelor's or final year of graduate program.
  • Excellent communication skills (verbal & written).
  • Ability to work effectively in a team.

Responsibilities

  • Provide support for post-market complaint investigations.
  • Assist in inspection planning and requirements generation.
  • Facilitate resolution of product non-conformities.
  • Support risk management files creation/assessment.
  • Assist in creation of Quality Management System (QMS) SOPs.
  • Support corrective and preventive action projects.
  • Participate in corrective action projects.
  • Apply Quality System standards.

Skills

Communication skills
Organizational skills
Interpersonal skills

Education

Pursuing a bachelor’s or master’s degree in Mechanical Engineering, Biomedical Engineering, Materials Science or equivalent

Job description

Quality Assurance Intern

Department: Quality

Employment Type: Internship

Location: Gainesville, FL

Reporting To: Sr. Manager Supplier Quality

Description

The primary scope of this internship is to assist the QA Engineering team with various projects, pushing forward a lean and efficient Quality program.

Key Responsibilities
  • Provide support for post-market complaint investigations
  • Provide support for inspection planning and requirements generation, manufacturing quality planning, and execution.
  • Provide support to facilitate resolution of product non-conformities.
  • Provide support for risk management files and their creation/assessment.
  • Assist in the planning, creation, and execution of automated programs and measurement systems analysis (MSA).
  • Assist in the creation of Quality Management System (QMS) SOPs, Wis, and Forms.
  • Assist in corrective and preventive action projects as necessary.
  • Know and apply the Quality System and any appropriate Federal and International standards.
  • Assist and support other employees, teams, and sales personnel as necessary.
Skills, Knowledge and Experience

Education:

  • Pursuing a bachelor’s or master’s degree in Mechanical Engineering, Biomedical Engineering, Materials Science or equivalent from an accredited institution required

Experience:

  • Must be enrolled in either Junior or Senior year of their Bachelors or final year of their graduate program in Mechanical, Biomedical, or Material Sciences.
  • Must have excellent communication (verbal & written) and organizational skills.
  • Must have excellent interpersonal skills and must be able to work effectively in a team environment.
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