Quality ControlAssurance Specialist Intern

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 Bachelors or Masters 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 Youll 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.