Quality Assurance Technician 2nd Shift

Quva • Sugar Land, TX

5d • Onsite

About The Position

The Quality Assurance Technician performs basic quality assurance functions to support the quality and safety of pharmaceutical products. After completing training, the role includes verifying incoming materials, checking labels, overseeing support areas such as preparation and label printing, and ensuring manufacturing areas are set up properly. The on-the-floor quality team ensures processes and documentation records comply with requirements, with patient safety, efficiency, quality, safety, and on-time delivery as priorities.

This is a full-time, onsite position in Sugar Land, Texas, on a consistent Monday-through-Friday second-shift schedule from 2:00 PM to 10:30 PM. Minimum overtime requirements apply; occasional weekend and overtime opportunities may also be available with advance notice. The position is safety sensitive and may be subject to random drug testing in accordance with applicable laws.

Requirements

• High school diploma or equivalent.
• Successfully complete a drug and background check.
• Ability and willingness to walk, stoop, stand, bend, and lift up to 50 pounds throughout each shift, with or without reasonable accommodation.
• At least 18 years of age.
• 20/20 vision, with or without corrective lenses, and ability to pass a color vision test.
• Familiarity with and comfort using mobile devices such as smartphones, tablets, and handheld devices.
• Currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas.
• Detail-oriented with strong verbal and written communication skills.
• Ability to demonstrate energy and accountability and to multitask.
• Ability to fulfill expectations, build sustainable relationships with team members, and maintain effective communication.
• Good interpersonal skills and ability to work effectively and efficiently in a team environment.

Nice To Haves

• 0 to 2 years of experience with FDA-regulated operations (cGMP processes) or Quality Assurance.

Responsibilities

• Ensure applicable U.S. regulatory requirements are met in procedures and practices.
• Review and verify critical information related to receipt of incoming goods and distribution of finished goods for customer orders.
• Ensure incoming materials comply with requirements before use in manufacturing operations.
• Verify that labels meet batch-record requirements and company standards.
• Ensure components and equipment used in manufacturing meet company cleanliness standards.

Benefits

• 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.
• Future career advancement opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED