Quality Control/Assurance Specialist Intern

Molekule

Date: 1 day ago
City: Lakeland, Florida
Contract type: Intern
Description

Summary:

Molekule is seeking a detail-oriented and highly motivated Quality Control/Assurance Intern to join our team. As an intern, you will support the Quality team in ensuring that products and processes meet established quality standards. This is an excellent opportunity to gain hands-on experience in quality management systems, regulatory compliance, auditing, and continuous improvement initiatives in a FDA Class II Medical Device work environment.

Responsibilities

  • Assist in the implementation and monitoring of quality control procedures and work instructions.
  • Conduct inspections and tests on materials, products, and processes to ensure compliance with specifications.
  • Record and analyze test data; prepare reports and document findings within eQMS.
  • Support the investigation of non-conformities and assist in root cause analysis and corrective action activities.
  • Help maintain accurate and up-to-date quality documentation and records (SOPs, work instructions, audit findings, etc.).
  • Participate in internal audits and assist with external audit preparation.
  • Collaborate with cross-functional teams to support quality improvement initiatives.
  • Learn company and federal safety policies and regulations.

Requirements

Qualifications:

  • Currently pursuing a Bachelor’s or Master’s degree in Engineering, Applied Sciences, Manufacturing, or a related field.
  • Strong attention to detail and analytical skills.
  • Excellent communication and organizational abilities.
  • Familiarity with quality tools (e.g., 5 Whys, Pareto analysis, fishbone diagrams) is a plus.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  • Ability to work both independently and as part of a team.
  • Previous coursework or experience in quality systems or compliance is a bonus.

What You’ll Gain

  • Hands-on experience in a professional QA/QC environment.
  • Exposure to Class II Medical Device industry standards and regulatory requirements (e.g., ISO, GMP, FDA)
  • Mentorship from experienced professionals.
  • Opportunity to contribute to real-world projects and quality initiatives.
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