Our Quality Control Data Reviewer 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 performing review of QC testing data for conformance to methods, SOPs, cGMP and Good Documentation Practices. 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 2nd shift, working Monday through Friday from 2pm to 10:30pm. 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 Quality Control Data Reviewer Does Each Day
- Reviews analytical testing of finished sterile products, and raw materials, following all written procedures and cGMP, and providing assurance of accurate documentation of analyses
- Conducts and writes laboratory investigations, with support from the Manager
- Verifies appropriate documentation for DEA controlled sample handling
- Documents completion of review and approval of data in the appropriate laboratory systems
- Reports any issues to the Supervisor upon discovery
- Partners with their Supervisor to understand overall expectations and execute them independently based on the prioritization of projects
- This individual will work with the Supervisor or Manager to understand overall expectations and provide data to meet project milestones
- Reads and understands SOPs and follow policy, procedure, and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements
- Provides review of analytical data in a timely manner
- Provides input to SOPs to enhance the efficiency of the laboratory
- Keeps up to date on SOPs, cGMP, and current Good Documentation Practices (cGDP) requirements
- Communicates as needed any testing issues to either a supervisor or manager or to a cross-functional group such as Metrology
- Recommends to Supervisor or Manager improvements to analytical test methods or documentation
Our Most Successful Quality Control Data Reviewer
- Detail-oriented with strong verbal and written communications skills
- Highly organized
- Knowledgeable in Microsoft Word and Excel
- Fulfills expectations, establishes sustainable relationships with team members, maintains effective and meaningful communication channels
Minimum Requirements For This Role
- 18+ years of age
- Able to successfully complete a drug and background check
- B.S. degree or higher in Chemistry, Biology, or related field
- 3 or more years of laboratory experience in the Pharmaceutical Industry
- 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
- Experienced with Waters H-class HPLC and Empower software
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
- 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.”
