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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 10:30. 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
• Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
• 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
• The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions
• Range: $74,766- $102,817 per Year

About Quva:

Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva’s overall product and technology offerings help health-systems achieve greater value and deliver the highest-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.”