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Principal Scientist, QC Compliance

Job in Bloomsbury, Hunterdon County, New Jersey, 08804, USA
Listing for: Quva
Full Time position
Listed on 2026-06-06
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below
Location: Bloomsbury

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
  • 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 provides 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 implements 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:
    • 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 practices
  • Drives 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,…
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