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Curia

End-to-end drug development and manufacturing

Quality Disposition Supervisor

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRensselaer, NY, USA$102k - $130k /yrIn-person

About the Job

Requirements

  • A bachelor's degree in science or a related study is required.
  • At least six years of Good Manufacturing Practice (GMP) experience in an FDA-regulated pharmaceutical environment is required, including at least four years of experience in quality disposition reviews and two years in a supervisory role.
  • Candidates must pass a background check and drug screen; an occupational health screening may also be required.
  • The role requires the ability to work promptly and under pressure to meet customer and business deadlines associated with batch record lot release.
  • The role requires strong attention to detail.
  • The role requires active identification and addressing of potential hazards, following established safety protocols, and participation in safety training programs.

Responsibilities

  • Act as the point of contact for product disposition.
  • Objectively and comprehensively review disposition packages and drive quality decisions related to product disposition, using data, sound technical and scientific rationale, data integrity requirements, and applicable regulatory and site procedural requirements.
  • Ensure batch records are thoroughly reviewed before product disposition to the customer within established timelines.
  • Ensure closure of deviations, corrective and preventive actions (CAPAs), change controls, and customer complaint investigations related to Curia-New York client products.
  • Interface with cross-functional departments to resolve batch record review comments in a compliant manner.
  • Serve as the key contact for product disposition questions during customer audits and regulatory inspections.
  • Act as the subject matter expert for quality issues related to batch release.
  • Develop a quality disposition and batch record reviewer qualification program.
  • Create a training feedback loop from batch record reviews with manufacturing and other cross-functional teams to drive continuous improvement.
  • Lead the team responsible for batch dispositions and lead site disposition reviews to meet supply commitments.
  • Serve as the primary gatekeeper for the site's disposition process, ensuring disposition-related batch record reviews are compliant, deviations are closed, QC data is reviewed according to procedures, and open change controls and CAPAs tied to batch disposition are assessed and their impact documented.
  • Ensure breakdown and demand-maintenance work orders affecting a batch are reviewed before disposition and that quality impact assessments are documented.
  • Mentor, guide, and advise team members and provide guidance and coaching sitewide.
  • Promote a safe and healthy work environment by identifying and addressing potential hazards, following safety protocols, participating in safety training, and fostering awareness and responsibility among team members.

About the Company

Curia

End-to-end drug development and manufacturing

Curia is a contract development and manufacturing organization (CDMO) that partners with pharmaceutical and biotech companies to move medical breakthroughs from concept to market. It provides end-to-end services across the drug development lifecycle, including early research, method development and validation, preformulation, material science, solid-state chemistry, and package device testing. Revenue comes from service contracts for specialized capabilities and expertise, with clients ranging from small startups to large pharma. Curia also collaborates with industry leaders to advance continuous flow development and manufacturing programs. The company differentiates itself through flexible and scalable solutions, deep scientific expertise, and state-of-the-art technology that help clients accelerate development timelines while navigating discovery to commercialization. Its goal is to enable efficient, reliable progression of drug candidates from conception through to market approval.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Albany, NY
Founded
1991

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