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Curia

End-to-end drug development and manufacturing

Quality Control Lab Technician 1

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeHopkinton, MA, USA$22.50 - $28.25 /hrIn-person

About the Job

Requirements

  • High school diploma or general education degree (GED).
  • A minimum of 0–1 years of relevant experience in a pharmaceutical testing laboratory.
  • Must pass a background check.
  • Must pass a drug screen.
  • May be required to pass Occupational Health Screening.

Responsibilities

  • Perform microbiological testing (endotoxin and bioburden) for water.
  • Perform microbiological testing (endotoxin, sterility, and bioburden) for raw materials, in-process materials, intermediates, and final product.
  • Perform environmental monitoring of clean rooms under USP and EU specifications.
  • Review documentation, analytical chromatographic data, and results from instrumental testing such as DSC, XRPD, water analysis, and USP testing for compliance with cGMPs, Curia SOPs, and other written procedures.
  • Analyze data for stability trends and deviations to ensure consistency with historical time points and prevent unexpected results.
  • Manage timelines and multiple projects by interfacing with scientists and management to coordinate testing timelines, corrections to documentation, and reporting within defined turnaround times; adjust priorities based on due dates and invoicing goals.
  • Assist in writing stability protocols.
  • Interact with outside testing laboratories to coordinate shipment and testing of stability samples.
  • Communicate technically with primarily external customers to report results, engage in technical discussion, and address questions.
  • Review and format reports such as Stability Summary tables to ensure accuracy and compliance with current Curia formats.
  • Manage invoicing for stability, including issuing BRFs, working with finance to ensure accurate and complete accounting for stability projects, reviewing monthly invoices, and tracking monthly and quarterly financial projections.
  • Handle controlled substances, including maintaining inventory, completing paperwork, and conducting biannual review.
  • Manage workload and time to perform multiple projects effectively and ensure all necessary paperwork is completed on time.
  • Assist with other tasks in the analytical function not directly related to specific projects.
  • Participate in self-development activities and train others.
  • Write proposals and design studies for stability.

Desired Qualifications

  • A bachelor's degree in chemistry, biology, or a related science.

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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