Production Technician I - Formulation 2nd Shift
Quva
Summary
Our Production Technician I – Formulation plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical product. Once you complete our training, your responsibilities will include supporting daily manufacturing activities for non-sterile and sterile bulk/CSP operations. 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 2nd shift, working Monday through Friday from 2:00 PM-10:30 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 Production Technician I – Formulation Does Each Day:
- Weighing of chemicals to support product formulation
- Formulation of bulk intermediate solutions
- Sterile filter integrity testing
- Clean Room cleaning and disinfection
- Perform equipment calibration checks
- Daily Supply list for respective area turned into receiving by scheduled time
- Open/close Formulation pods and ILP in accordance with work instructions and daily task lists
Our Most Successful Production Technician I – Formulation:
- Approach others in a tactful manner
- React well under pressure
- Follow through on commitments
- Carefully follows clear directions to ensure safety and accuracy
- Are detail-oriented and take careful notes
- Take initiative to identify problems and opportunities
- Have strong math skills
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
- Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
- Requires extensive training and qualification including but not limited to: gown training; aseptic technique; competency assessments; direct observation; and media fill qualification for each compounding process
- Strong math skills
- 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
Any of the Following Will Give You an Edge:
- College Degree with an emphasis in Chemistry, Biochemistry or equivalent
- 1 year of pharmaceutical manufacturing experience
- Working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs
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
- Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
- Requires extensive training and qualification including gown training, aseptic technique, competency assessments, direct observation, and media fill qualification for each compounding process
- Strong math skills
- 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
Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- 401(k) Matching
- Paid Time Off
- Paid Holidays
- Consistent Full-Time Schedule
- 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.