Our Inspection, Labeling and Packaging (ILP) 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 meticulously inspecting, labeling, and packaging our products according to strict industry regulations and company standards. Your attention to detail and adherence to precise procedures will guarantee that our medications reach patients accurately and securely. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
This is a full-time role for our 1st shift, working Monday through Friday from 7AM to 3:30PM. 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.
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What The ILP Technician Does Each Day
- Prepare work areas, gather supplies, and maintain strict cleanliness standards
- Inspect, label, and package products according to standard operating procedures (SOPs)
- Maintain accurate documentation and adhere to quality and compliance standards
- Notify management of any deviations from established processes
- Cleans, organizes, and stocks supplies
Our Most Successful ILP Technicians
- Enjoy working independently
- Carefully follow clear directions to ensure safety and accuracy
- Are detail-oriented and take careful notes
- Support others when needed with activities like cleaning, stocking, etc.
- 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 40 lbs. throughout each shift, with or without reasonable accommodation
- 20/20 vision with or without corrective lens
- Able and willing to follow strict clothing and accessory rules to support our sterile operating environment
- Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
- 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, attention to detail and individualized work - such as working in a warehouse or manufacturing environment
- Experience in a pharmaceutical manufacturing environment
- Working in or around a sterile “cleanroom”
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.”
