Quality Assurance & Compliance Intern

Simtec Silicone Parts • Miramar, FL

20h • Onsite

About The Position

The intern will assist with rebuilding and organizing critical quality and operational documentation following a cybersecurity recovery initiative. This role offers valuable exposure to document control systems, quality management processes, and cross-functional collaboration within a manufacturing environment. The intern will be assigned a dedicated mentor within the Quality & Engineering Department and will participate in weekly one-on-one coaching and development meetings to review progress, discuss learning objectives, and receive professional feedback.

Requirements

• Pursuing a degree in Industrial Engineering, Mechanical Engineering, Quality Engineering, Business Operations, or related field.
• Junior or Senior academic standing preferred.
• GPA of 3.0 or above preferred.
• Strong attention to detail and organizational skills.
• Proficiency in Microsoft Excel and Microsoft Office.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities in a fast-paced environment.
• Document Control
• Quality Assurance
• Microsoft Excel
• Attention to Detail
• Quality Management Systems (QMS)
• Technical Documentation
• Organizational Skills
• Process Documentation
• Communication Skills
• Continuous Improvement

Nice To Haves

• Understanding the fundamentals of Quality Management Systems (QMS).
• Exposure to ISO 9001 and ISO 13485 requirements.
• Learning document control and revision management processes.
• Developing skills in compliance documentation and record retention.
• Participating in continuous improvement initiatives.
• Gaining experience working in a regulated manufacturing environment.
• Improving professional communication and project management skills.

Responsibilities

• Analyze, improve, and standardize quality system documentation to support compliance with ISO 9001 and ISO 13485 requirements.
• Support document control activities within the Quality Management System (QMS).
• Assist with maintaining accurate records and revision controls.
• Help standardize file structures and document naming conventions.
• Support validation documentation activities.
• Collaborate with Engineering, Quality, and Production teams on documentation updates.
• Assist in ensuring compliance with internal procedures and customer requirements.
• Support the migration and standardization of quality documentation.
• Develop a document retention and indexing methodology.
• Assist in the review of Standard Operating Procedures (SOPs).
• Participate in internal quality improvement initiatives.
• Create metrics dashboards related to document control effectiveness.

Benefits

• Exposure to manufacturing quality systems and document control
• Hands-on experience within a regulated manufacturing environment
• Practical experience working with SOPs, work instructions, and validation documentation
• Cross-functional collaboration experience

What This Job Offers

• Career Level: Intern
• Education Level: No Education Listed