Production Technician I - Ilp 2Nd Shift

Production Technician I  ILP 

Inspection, Labeling and Packaging (ILP) Technician: About This Role

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 2nd Shift, working Monday through Friday from 2:00 PM to 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.

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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
• 20/20 vision with or without corrective lens
• Able to successfully complete a drug and background check
• 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
• Able and willing to walk, stoop, stand, bend, and lift throughout each shift, with or without accommodation
• 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 Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.

As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.

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.”