Principal Scientist, QC Compliance

Job description

NJ - Bloomsbury Site

519 NJ-173

Bloomsbury, NJ 08804, USA

Description

The Principal Scientist, QC Compliance serves as a senior technical and compliance leader within the Quality Control organization, providing strategic oversight of laboratory compliance, data integrity, and performance across analytical and microbiology functions. This role is responsible for ensuring QC operations consistently meet cGMP, GDP, FDA 503B, and regulatory expectations while driving inspection readiness, continuous improvement, and operational excellence. This position partners cross-functionally with Quality Assurance, Manufacturing, Technical Services, and Regulatory Affairs to strengthen quality systems, improve laboratory performance, and ensure sustainable compliance. 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.

This is an on-site role in Bloomsbury, New Jersey.

What the Principal Scientist, QC Compliance Does Each Day:

Serves as the subject matter expert (SME) for QC compliance across analytical chemistry and microbiology laboratories

Ensures all QC activities comply with cGMP, GDP, SOPs, and regulatory requirements

Provides oversight for laboratory equipment life cycle management, computer system validation and data integrity standards

Leads initiatives to enhance compliance frameworks, inspection readiness, and audit outcomes

Owns and monitors QC laboratory dashboards and KPIs, including:

Performs trend analysis of lab events, deviations, and investigations to identify systemic issues and recommend corrective actions

Drives improvements in laboratory efficiency, turnaround time, and Right First Time (RFT) performance

Leads and provide technical oversight of complex laboratory investigations (OOS, OOT, deviations, and customer inquiries)

Ensures investigations are scientifically sound, compliant, and completed within established timelines

Identifies recurring issues and implement robust CAPAs to prevent recurrence

Supports QC inspection readiness efforts and internal/external regulatory inspections

Acts as SME, within areas of responsibility, during FDA, customer, and internal audits

Ensures audit findings are addressed with compliant corrective actions

Oversees and provides guidance on:

Ensures compliance with regulatory standards, industry best practices and internal quality standards

Supports the development and implementation of QC training programs and technical training modules

Mentors and coaches QC scientists and analysts on compliance expectations and best practicesDrives a culture of data integrity, quality ownership, and continuous learning

Leads operational efficiency and process improvement initiatives across QC laboratories

Supports capacity planning and utilization optimization

Drives or supports strategic projects (e.g., specification harmonization, system enhancements)

Authors, reviews, and approves SOPs, protocols, and reports to ensure regulatory compliance

Our Most Successful Principal Scientist, QC Compliance has:

Deep expertise in cGMP, GDP, FDA 503B regulations, and laboratory compliance requirements

Working knowledge of CFR, Eudralex, FDA guidance documents, ICH, ISO and Compendia

Strong analytical problem-solving skills with ability to interpret complex data sets

Demonstrated experience leading investigations, deviation management, and CAPA effectiveness

Advanced understanding of analytical chemistry and microbiological testing principles

Proven ability to influence cross-functional teams and drive compliance improvements

Strong communication skills, including interaction with regulatory agencies and auditors

High level of attention to detail and commitment to data integrity

Experience with LIMS, Empower, and laboratory data systems preferred

Experience analyzing data and preparing data summaries using software, such as JMP and Minitab

Experience working with project management software is a plus

Minimum Requirements for this Role:

Legally authorized to work in the job posting country

Bachelor’s degree in Chemistry, Microbiology, Pharmaceutical Sciences, or related field required

Master’s or PhD preferred

10+ years of experience in pharmaceutical QC, QA, or compliance within a cGMP-regulated environment

Significant experience in analytical and/or microbiology laboratory operations

Demonstrated leadership in regulatory inspections, audits, and compliance remediation

Experience with method validation, stability programs, and lab investigations required

18+ years of age

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:

Experience in 503B outsourcing facilities or sterile manufacturing environments

DEA compliance exposure (controlled substances)

Lean/continuous improvement certification or experience

Benefits of Working at Quva:

Comprehensive health and wellness benefits including medical, dental and vision

401k retirement program with company match

12 PTO, 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, certifications, geographic location, and market conditions

Range: $113,754 - $177,695 Annually

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 BrightStreampartners 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.”

Equal Opportunity Employer

This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.

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Who can apply

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