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QuVa - Advancing Healthcare Possibilities

Director, Quality Control Lab

Bloomsbury, NJ, United States

$163,764 to $255,881 USD / year

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Job details

Pay: $163,764 to $255,881 USD / year
Experience: Ten years of analytical chemical/microbiology laboratory and 5 years of management experience
Posting language: English
Posted: Nov 5, 2026

Original job description

Our Director, Quality Control Lab, plays a vital role within our organization. Once you complete our training, you will be responsible for day-to-day operations of the Quality Control testing laboratories supporting all Quva production sites. This position also coordinates, leads group activities, and develops and implements the department's short and long-term goals to assure compliance with cGMPs and agreement with Quva business initiatives. The Director, Quality Control Lab, manages and develops teams within the department to support Company activities. This role also serves as a technical expert for the site in the areas of chemistry, analytical methods, microbiology and test method transfer. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. 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 an on-site role located in Bloomsbury, NJ with travel to Sugar Land, Texas.

What the Director, Quality Control Lab Does Each Day:

Prepares resource analysis for the execution of projects; Prepares and manages the Department operational budget
Establishes and maintains effective cross functional relationships; Provides necessary support to other Departments
Provides leadership in the training program of laboratory staff; Evaluates subordinates through reviews and periodic discussions; Recommends future development objectives; Fosters teamwork, customer service and cross-functionality
Prepares/reviews/approves departmental documentation (i.e. SOPs, Analytical Method Transfer protocols)
Assures that departmental SOPs are followed and are compliant with current Good Manufacturing Practices (cGMP) and Company policies; Operates the laboratories in a safe and hazard-free manner
Leads the routine Quality Control release testing laboratories to ensure testing is completed on time in a compliant manner
Leads the corporate Stability laboratory to ensure products meet their BUD and with establishing BUD for new products
Applies fundamental knowledge of Analytical Chemistry and advanced technologies in analysis, interpretation and understanding of test results, for both qualitative and quantitative analyses
Provides expertise and assists in writing investigation reports for Laboratory investigation, Operations investigations, and Cross-functional investigations
Recommends or makes changes to tests, assays and specifications to ensure reliability, accuracy and their adequacy for the monitoring of product quality
Provides customer support as needed

Our Most Successful Director, Quality Control Lab:

Has outstanding written and oral communication skills
Is excellent at organization of large volumes of data
Has experience in pharmaceutical manufacturing preferably sterile injectable
Manages multiple, parallel projects
Has Expert knowledge of regulatory requirements as they pertain to Human Drug Compounding and Pharmaceutical manufacturing

Minimum Requirements for this Role:

A. /B.S. Degree in Chemistry, Biochemistry, Microbiology or related field with significant experience
Ten years of analytical chemical/microbiology laboratory and 5 years of management experience
Pharmaceutical laboratory experience in analytical methods development and validation area is expected
Able to successfully complete a drug and background check
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:

Has experience with manufacturing parenteral products
Has experience in QA/QC

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
20 + 5 PLP 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
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: $163,764 - $255,881 Annually
This role is also eligible for an annual incentive bonus, subject to program terms and guidelines

About Quva:

Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma’s multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva’s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver 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.”

California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

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More about this job

Skills

Quality control
Process improvement
Attention to detail
Leadership
Teamwork
Customer service
Documentation
Good manufacturing practices
Analytical chemistry
Communication skills
Pharmaceutical processes

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