INTERNSHIP DETAILS

Quality Control/Assurance Specialist Intern

CompanyMOLEKULE GROUP, INC
LocationLakeland
Work ModeOn Site
PostedApril 29, 2026
Internship Information
Core Responsibilities
The intern will support the quality team by monitoring quality control procedures, conducting inspections, and documenting findings within the eQMS. They will also assist in investigating non-conformities and participating in internal and external audit preparations.
Internship Type
full time
Company Size
80
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
You track your sleep. Filter your water. Eat organic. But what about the air you breathe? Most people spend 90% of their lives indoors, breathing allergens, chemicals, bacteria, and pollutants invisible to the naked eye. Air affects how you sleep, focus, and feel. And yet it’s one of the least talked about aspects of health. Molekule’s mission is to change the world from the indoors out. Helping people understand, monitor, and improve the air around them. Because when you breathe better air, you feel it. Built on 25 years of research and development, Molekule is home to PECO, proprietary technology that goes beyond just capture: it destroys them at the molecular level. PECO works with HEPA filtration to reduce pollutants in your air, including viruses, bacteria, mold, VOCs, and more. Air is the foundation of wellness. Come feel the difference.
About the Role

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.


What You Will Own:

  •  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

What You Will Bring:

  •  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.

PHYSICAL REQUIREMENTS:

Physical demands of this position include, but are not limited to sitting, standing, walking, climbing, kneeling, twisting, reaching, bending, lifting up to 50 pounds, carrying, pushing, pulling, dexterity of utilizing hands and fingers, ability to work in a manufacturing environment, ability to work onsite, seeing (close vision, distance vision, color vision, peripheral vision and depth perception), hearing and speaking.


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.
Key Skills
Quality controlQuality assuranceRegulatory complianceAuditingContinuous improvementRoot cause analysisCorrective actionSOP documentationData analysisMicrosoft Office Suite5 WhysPareto analysisFishbone diagramsMedical device regulationsGMPISO
Categories
EngineeringManufacturingHealthcareScience & Research
Benefits
Hands-on experience in a professional QA/QC environmentExposure to Class II Medical Device industry standardsMentorship from experienced professionals