Lead Quality Assurance Specialist

3 weeks ago


Bloomsbury, New Jersey, United States QuVa Pharma Full time

Unlock a fulfilling career as a Lead Quality Assurance Specialist with QuVa Pharma, where you'll play a vital role in ensuring the highest quality and safety standards of our pharmaceutical products.

About the Role

We're seeking an experienced Quality and Compliance Investigator to join our team. As a key member of our quality assurance team, you'll be responsible for conducting thorough investigations into deviations and incidents, implementing corrective actions, and collaborating with cross-functional teams to drive process improvements.

About QuVa Pharma

QuVa is a national, industry-leading provider of pharmacy services, delivering essential medications in injectable formats critical for effective patient care. Our innovative solutions, including ready-to-administer sterile outsourcing and advanced AI-generated insights, empower health systems to transform pharmacy management and achieve greater value in patient care.

What You'll Do Each Day
  • Autor and resolve deviations in order to meet production and product release requirements
  • Communicate across multiple groups and levels to drive deviation closure
  • Identify interdepartmental process improvements and work cross-functionally to implement them
  • Utilize advanced root cause analysis techniques and technical impact analyses during the deviation investigation process
  • Manage multiple priorities either independently or as part of a team in order to meet key deadlines and communicate issues and progress across all levels of organization
Requirements for Success
  • 18+ years of age
  • An associate degree and 3+ years' cGMP experience OR
  • A Bachelor's degree and 2+ years' cGMP experience
  • Experience with authoring, writing, and leading deviation investigations
  • Experience working within a production or quality department of a pharmaceutical/manufacturing company
  • Knowledge of continuous improvement techniques and problem-solving skills
  • Ability to work extended and flexible hours (including weekends) when needed
  • 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
Benefits and Perks
  • $65,000 - $85,000 per year, based on experience
  • 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


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