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Curia

End-to-end drug development and manufacturing

Material Control Specialist 1

Shipping & ReceivingConfirmed live in the last 24 hours
Full-timeRensselaer, NY, USA$60.9k - $75.2kIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • A minimum of 0–3 years of relevant experience is required.
  • The employee must be willing to work with chemicals.
  • The employee must have good written and verbal communication skills and be able to coordinate diverse responsibilities.
  • The employee must become Curia respirator certified and qualify for medical clearance to handle raw and finished materials.
  • The employee must be able to use the metric system for mass and volume and physically perform the position's duties.
  • The employee must be able to lift or move up to 10 pounds regularly, up to 25 pounds frequently, and up to 50 pounds occasionally.
  • The employee must have the vision abilities required for the work, including close, distance, color, peripheral, and depth vision.

Responsibilities

  • Load box and flatbed trailers from a loading dock.
  • Communicate with truck drivers to off-load box and flatbed trailers.
  • Unbox and visually inspect packaging, verify that paperwork is correct, and ensure proper documentation has been provided with submission forms.
  • Receive GMP and non-GMP materials into Oracle EBS and use computer systems, including email and Oracle, to respond to and make requests supporting business operations.
  • Label materials and generate applicable GMP paperwork.
  • Use the chemical inventory database for non-GMP materials.
  • Move materials within, to, and from the warehouse; verify correct lots and material descriptions; and move materials as requested by a supervisor.
  • Work independently, prioritize workload, meet tight deadlines, complete GMP documents accurately, and maintain logbooks.
  • Dispense bulk material according to customer requests, complete shipping requests, and submit samples promptly.
  • Handle hazardous materials.
  • Organize and deliver non-GMP items, including process equipment weighing less than 300 pounds and laboratory chemicals.
  • Communicate to determine and notify the applicable department about incoming material samples from outside vendors or inter-office sources.
  • Operate a handheld barcode transmitter to identify and locate materials.
  • Perform housekeeping to maintain a safe, clean, and organized warehouse work and storage area.
  • Maintain documentation, safety practices, and knowledge of GMP and non-GMP policies.
  • Participate in cross-training, self-development activities, and training others.
  • Exhibit safety awareness and safe work practices.
  • Recommend and implement methods to improve product or service quality, reduce costs, and identify safety opportunities.
  • Comply with Curia standard operating procedures, safety guidelines, and applicable regulatory guidelines.

Desired Qualifications

  • An advanced degree is preferred.
  • Previous warehouse or pharmacy experience is preferred.
  • Certification in powered industrial fork truck operation in accordance with 29 CFR 1910.178 is preferred.

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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