What are the responsibilities and job description for the Quality Control/Assurance Specialist Intern position at Molekule?
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
What You Will Bring:
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
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.
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 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.