Quality Assurance Technician 2nd Shift
Quva
Summary
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 performing 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!
Job description
This is a full-time role for our second shift, working Monday through Friday from 3:00 PM-11:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.
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
Requirements
- 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
- 0 to 2 years' experience with FDA-regulated operations (cGMP processes) or Quality Assurance
Benefits
- Medical, Dental & Vision
- 401(k) Matching
- 17 Paid Days Off
- 8 Paid Holidays
- Set Full-Time Schedule
- Overtime Opportunities
- Career Advancement Opportunities
Company overview
Quva is a national, industry-leading provider of health-system pharmacy services and solutions, operating at the intersection of pharmaceutical manufacturing and healthcare analytics. Founded in 2015 and headquartered in Sugar Land, Texas, the company has established itself as a prominent player in the 503B sterile injectable outsourcing market. Quva operates FDA-registered 503B outsourcing facilities that provide hospitals with essential medications in ready-to-administer formats, leveraging cGMP expertise and pharmaceutical manufacturing capabilities across multiple production facilities. The company's comprehensive platform combines sterile injectable compounding with advanced data analytics through its Quva BrightStream division, which offers AI-powered predictive analytics and data insights software solutions. These tools help health systems aggregate, normalize, and analyze complex data across care sites, supporting revenue optimization, script capture, inventory management, and drug shortage control. With over 1,000 employees and serving more than 3,500 health systems nationwide, Quva has secured significant funding, including a $275 million debt financing round in 2021. The company's integrated approach transforms pharmacy management by enabling healthcare providers to operate more efficiently and effectively while delivering high-quality patient care.