Production Technician I - ILP 2nd Shift
Quva
Summary
Support execution of product visual inspection, labeling and packaging (ILP) operations at the Quva facility in accordance with established processes and procedures.
Job description
What the ILP Technician Does Each Day
- Assists preparation of inspection and packaging room materials supplies
- Conducts labeling and the processing of production materials as required
- Daily/Bi-Weekly/Monthly cleaning of room and equipment and fills out appropriate preventative maintenance forms and checklists in accordance with SOPs
- Conduct and complete line and room clearances as per established procedures
- Completes necessary documents for accountability and traceability of products following Good Documentation Practices (GDPs); comply with cGMPs and company ISO standards
- Complies with 503B guidelines; cGMPs, standard operating procedures and company policies
- Performs equipment calibration checks and troubleshoots production equipment as needed
- Completes documentation of activities in accordance with established procedures
- Immediately notifies production management of deviations to established processes or procedures
- Assists other areas as needed (cleaning; non-sterile filling; kitting and preparation operations, etc.)
- Primary, secondary, and tertiary labeling of products
- Secondary and final packaging of product
- Requires visual inspection of product
- Maintains inspection ready environment and supports internal/external audits
Our Most Successful ILP Technicians
- Promotes active listening with team members; strong verbal and written communication skills with the ability to work effectively with other departments and people at all levels
- Understands how various issues affect each other and the outcome of projects; mechanical aptitude a plus
- Effectively and productively engages with others and establishes trust, credibility, and confidence
- Listens to internal customers, ensures commitments are met, sets appropriate internal customer expectations
- Has working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs
- Follows policies and procedures; completes administrative tasks correctly and on time
- Approaches others in a tactful manner; reacts well under pressure; treats others with respect; accepts responsibility for own actions; follows through on commitments
- Has strong attention to detail
- Is flexible and can adapt to support multiple production areas and shifts as needed
Minimum Requirements for this Role
- High school Diploma or GED from recognized institution or organization required
- Will be required to undergo a color perception exam and must be able to produce a passing test result
- Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction
- Able to successfully complete a drug and background check
- 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
- Pharmaceutical experience
Requirements
- High school Diploma or GED from recognized institution or organization required
- Will be required to undergo a color perception exam and must be able to produce a passing test result
- Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction
- Able to successfully complete a drug and background check
- 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
- Pharmaceutical experience preferred
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.