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Form of workOur Production Technician I - Prep 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 supporting the preparation of up-front processes of the manufacturing of compounded sterile preparations (CSPs) in accordance with established 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. 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 6AM to 2:30PM. 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.
What the Production Technician I – Prep 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:
- 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:
- 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
- Able to successfully complete a drug and background check
- High school Diploma or GED from recognized institution or organization required
- Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds.
- 18+ years of age
- Able and willing to walk, stoop, stand, bend, and lift throughout each shift, with or without accommodation
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)
- At least 1 year hospital or retail pharmacy experience
- At least 1-year pharmaceutical manufacturing
- CPhT Certification
- ACPE Sterile Certification
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.”
