Integral Molecular is a close-knit, medium-sized biotech company focused on developing and applying innovative technologies that advance vaccines and antibody therapeutics targeting difficult proteins. We are actively seeking a Quality Assurance Associate to uphold and champion the quality and reliability of our products and services. This role involves the refinement, oversight, and management of company-wide quality processes and procedures to continually strengthen our commitment to excellence. As we expand our portfolio of scientific offerings, we remain dedicated to maintaining our high standards of quality and performance for every project. If attention to detail and audit management are where you thrive, we would love to have you join our team!

Opportunities that this position offers you:

• Be a leader: Drive process optimization, document control, standardization, and compliance strategies across the entire company
• Expand your toolkit: Develop expertise in quality assurance and compliance areas
• Shape what's next: Your input will help shape the direction of our QA programs and infrastructure
• Certify your future: Opportunities for personal certification in Quality Auditor, Lean Six Sigma, etc.
  
  

What you will do at Integral Molecular:

• Implement standards and define quality processes and procedures through effective controlled documentation issue and management
• Manage the corporate Document Change Request (DCR) system for maintaining SOPs and worksheets across the company
• Schedule and conduct internal audits, prepare reports, and track corrective and preventive actions (CAPA)
• Perform audits of vendor and external service providers as part of the vendor selection and qualification process
• Host and manage customer audits and regulatory inspections, including preparation and responses
• Identify relevant quality-related training needs and deliver training where required
• Ensure the accuracy and quality of records and documents
  
  

The ideal candidate will have:

• BS in a scientific discipline (e.g., molecular biology, biochemistry, chemistry, biology)
• 2+ years in a QA/QC role with document control, auditing, or CAPA management preferred; experience with Quality Management Systems is a plus
• Organized, detail-oriented, and proactive
• Excellent communicator with ability to influence and collaborate across teams
  
  

Integral Molecular is an Equal Opportunity Employer.