Our Quality Assurance Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performs basic QA functions related to verification of incoming materials, label checks, and oversight of support areas (i.e. prep and/or label printing) to ensure the manufacturing areas are set up for success. The on-the-floor quality team is responsible for making sure the process and documentation records are compliant with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role!
This is a full-time role for our 1st shift, working Monday through Friday from 6:00 AM to 2:30 PM This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.
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What The Quality Assurance Technician Does Each Day
Ensure that all applicable US Regulatory requirements are being met within the procedures and practices
Quality review / verification of critical information related to the receipt of incoming goods or the distribution of finished goods for customer orders
Ensures compliance of incoming materials prior to use in Manufacturing Operations
Ensures verification of labels against batch record requirements complies with company standards
Ensures levels of cleanliness for components and equipment used in the manufacturing process meet the company standards
Our Most Successful Quality Assurance Technicians
Are detail-oriented with strong verbal and written communications skills
Express energy, show accountability, and multi-task
Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels
Have good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals
Minimum Requirements For This Role
A High School diploma or equivalent
Able to successfully complete a drug and background check
Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
18+ years of age
20/20 vision (with or without corrective lenses) and the ability to successfully pass a color vision test
Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas
Any Of The Following Will Give You An Edge
0 to 2 years’ experience with FDA-regulated operations (cGMP processes) or Quality Assurance
Benefits Of Working At QuVa
Set, full-time, consistent work schedule
Comprehensive health and wellness benefits including medical, dental and vision
401k 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
About QuVa
QuVa is a national, industry-leading provider of pharmacy services, including ready-to-administer sterile outsourcing and advanced AI-generated insights providing clarity for revenue capture and inventory management. QuVa Pharma delivers essential medications in injectable formats critical for effective patient care. LogicStream, a QuVa company, partners with health systems to aggregate, normalize, and analyze large amounts of complex data through AI and machine learning tools that generate actionable insights supporting revenue optimization, inventory management, and inventory-related workflows. Through QuVa’s integrated solutions, health systems can transform pharmacy management to achieve greater value by operating more efficiently and effectively as they deliver high-quality patient care.
QuVa is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. QuVa's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with QuVa is “at will.”
Seniority level
Entry level
Employment type
Full-time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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