Production Technician I - Clean Room Support 3rd Shift
Quva
Summary
Our Production Technician I – Prep/Cleanroom Support 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 assisting in Prep/Cleanroom operations at QuVa Pharma in accordance with established processes and procedures. Your 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.
Job description
This is a full-time role for our 3rd shift, working Monday through Friday from 10:00 PM to 6:30 AM. 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.
What the Production Technician I – Prep/Clean Room Support Does Each Day:
- Support cleanrooms, formulations, ILP, and compounding
- Assist in preparation, transportation, labeling, production, and processing of materials
- Daily/weekly/monthly cleaning of rooms and equipment while adhering to standards
- Maintain Aseptic Gowning Qualification to support cleaning
- Complete necessary documents for accountability and traceability of product following Good Documentation Practices (GDPs)
- Manage FEFO of chemicals, pulling expired ones monthly
- Complete documentation of activities in accordance with established procedures
- Perform sterile filter integrity testing as required
Our Most Successful Production Technicians I – Prep/Clean Room Support:
- Promote active listening with team members and enjoys collaboration
- Effectively and productively engages with others and establishes trust, credibility, and confidence with others
- Are Customer Oriented
- Take initiative to identify problems and opportunities
Minimum Requirements for this Role:
- A High School diploma or equivalent
- Able to successfully complete a background check
- Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
- Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
- Able and willing to follow strict clothing and accessory rules to support our sterile operating environment
- 18+ years of age
- 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:
- Experience in a role requiring repetitive tasks
- Experience in a pharmaceutical manufacturing environment
- Experience with Good Documentation Practices (GDPs)
- 1-year of pharmaceutical manufacturing
- CPhT Certification
- ACPE Sterile Certification
Requirements
- A High School diploma or equivalent
- Able to successfully complete a background check
- Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
- Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
- Able and willing to follow strict clothing and accessory rules to support our sterile operating environment
- 18+ years of age
- Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas
Benefits
- Set, full-time, consistent work schedule
- Comprehensive health and wellness benefits
- Medical, Dental & Vision
- 401(k) Matching
- 17 paid days off
- 8 paid holidays per year
- Occasional weekend and 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.