C

Curia

End-to-end drug development and manufacturing

Quality Control Trainer

Corporate & Technical TrainingConfirmed live in the last 24 hours
Full-timeRensselaer, NY, USA$88k - $110k /yrIn-person

About the Job

Requirements

  • A bachelor's degree with a concentration in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field, and 5–7 years of related work experience.
  • Experience training or mentoring in a regulated environment.
  • Strong organizational skills, attention to detail, prioritization, scheduling, time management, and deadline management.
  • Ability to communicate clearly in writing and speech, present engagingly and succinctly, and simplify complex technical concepts for a range of learners.
  • A coaching mindset and ability to provide constructive feedback and work with employees at different skill levels.
  • Problem-solving and root cause analysis skills.
  • Ability to collaborate with team members, subject matter experts, and other stakeholders and build productive working relationships.
  • Ability to apply user experience design principles to instructor-led training.
  • Familiarity with regulatory expectations, including Food and Drug Administration guidelines.
  • Ability to develop learning assessments, including using Kirkpatrick’s Model of Evaluation.
  • Experience with learning management system platforms and training documentation systems.
  • Must pass a background check and drug screen; may be required to pass occupational health screening.

Responsibilities

  • Develop and execute qualification programs for Quality Control techniques and instrumentation.
  • Serve as the single point of accountability for training new Quality Control employees and providing refreshers for existing Quality Control employees.
  • Analyze deviations, out-of-specification and out-of-trend results, and laboratory errors to identify training needs.
  • Ensure all training aligns with current Good Manufacturing Practice requirements and internal quality systems.
  • Design and deliver instructor-led and hands-on training for Quality Control analysts, including high-performance liquid chromatography, gas chromatography, wet chemistry, and dissolution; create and maintain training materials.
  • Develop structured multi-month onboarding programs for new hires and cross-training plans for existing staff.
  • Translate complex analytical methods and standard operating procedures into clear, trainable content.
  • Facilitate classroom and laboratory-based training sessions.
  • Reinforce data integrity principles, including ALCOA+, in all training activities.
  • Maintain training compliance in accordance with regulatory expectations, including audit readiness.
  • Assess analyst competency through observation, practical assessments, and knowledge checks.
  • Maintain training matrices and ensure timely qualification and requalification.
  • Implement training improvements to reduce repeat errors and improve right-first-time performance.
  • Partner with Quality Control management, Quality Assurance, and Manufacturing to align training with operational needs.
  • Ensure safety practices are followed during instructor-led training.
  • Perform other duties as assigned.

Desired Qualifications

  • Strong hands-on experience with analytical techniques such as high-performance liquid chromatography, gas chromatography, ultraviolet spectroscopy, and wet chemistry.

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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