Incoming Quality Assurance Technician Mid Shift

The Incoming Quality Assurance Technician position contributes to the organization by coordinating Incoming Quality Assurance (IQA) aspects of raw materials and sterile supplies for compounding pharmaceuticals. The role involves preprinted label receipt inspections and quality processes. It requires critical thinking and authority to proactively address and/or escape IQA issues. The Incoming QA Technician performs basic QA functions related to verification of incoming materials.

Attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a full‑time role for our mid shift, working Monday through Friday from 10 AM - 7 PM CST. It is a set, consistent schedule with minimum overtime requirements and is based at our Sugar Land, TX location.

This is a safety‑sensitive position that may be subject to random drug testing, in accordance with applicable laws.

• QC test steps in ERP system
• Inspection of bulk bags from other Quva sites
• Assist with the coordination of transfers between Quva sites
• Incoming environmental plate sampling or sending for testing
• Quality inspection and QC step in ERP of labels
• Quality inspections/sampling verification of raw materials and sterile supplies
• Quality review/verification of critical information related to the receipt of incoming materials
• Escalate any discrepancies or non‑conformances found during incoming receipt inspection
• Retrieve and request quality documents (CoA, CoC, CoS…) from vendors for incoming materials
• Ensure compliance of incoming materials prior to use in manufacturing operations
• Ensure company compliance to Quva Pharma's standard operating procedures (SOPs) and quality management system (QMS)
• Follow all regulatory guidelines and cGMP guidelines as required by the job function
• Ensure all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs
• Perform visual inspections of products to verify conformance to quality, safety, and regulatory standards
• Other duties as designated by Quality Management

• Understands updating of standard operating procedures, with documentation of summary of changes and version control
• Can manage projects coordinating cross‑departmental activities
• Is proficient in Microsoft Office, Adobe, Word and Excel
• Is detail‑oriented and possesses strong verbal and written communication skills

• A high school diploma or equivalent
• At least 2 years of experience in FDA‑regulated quality assurance, sterile compounding and/or GMP production facility
• 18+ years of age
• Required to undergo a color perception exam and pass the test
• Required to undergo a vision exam and pass with 20/20 vision with or without correction
• Able to successfully complete a drug and background check
• Must be currently authorized to work in the United States on a full‑time basis;
  Quva is not able to sponsor applicants for work visas

• Bachelor's degree in life science or equivalent work experience

• Set, full‑time, consistent work schedule
• Comprehensive health and wellness benefits including medical, dental and vision
• 401(k) retirement program with company match
• 17 paid days off plus 8 paid holidays per year
• Occasional weekend and overtime opportunities with advance notice
  
  National, industry‑leading high‑growth company with future career advancement opportunities

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