C

Curia

End-to-end drug development and manufacturing

Process Engineer 1

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeAlbuquerque, NM, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Biology, Chemical Engineering, or a related field of study is required.
  • Must pass a background check and drug screen.
  • Must be able to obtain and maintain gowning certification.
  • May be required to obtain and maintain media qualification and wear a respirator.
  • Ability to work with a moderate amount of supervision and interact well with clients and interdepartmental colleagues.
  • Strong communication skills and a meticulous, organized approach are required.

Responsibilities

  • Lead batch record and process activities for client-specific formulation and filling operations for at least one client.
  • Oversee critical engineering and good manufacturing practice operations, including equipment preparation, bulk product formulation, sterile filtration, and filling support.
  • Act as a subject matter expert for good manufacturing practice investigations, including corrective and preventive actions, departures, and change control requests, from initiation to closure.
  • Interact directly with clients in routine discussions and summarize engineering work verbally and in writing, with support from more senior engineers as needed.
  • Identify and specify process-specific equipment based on facility, client, and program needs.
  • Author instructions for equipment operation and process flows in the cleanroom facility.
  • Develop new procedures to meet facility and client requirements.
  • Adhere to safety requirements at all times.
  • Design and provide training on operational tasks captured in standard operating procedures or work instructions.
  • Provide training on client programs and processes.
  • Read and interpret standard operating procedures to ensure compliance and maintain up-to-date training.
  • Promote a safe and healthy work environment by identifying and addressing hazards, following safety protocols, participating in safety training, and fostering awareness and responsibility among team members.

Desired Qualifications

  • Process engineering experience is preferred.
  • A minimum of two years of experience in the pharmaceutical or biotech industry is preferred.
  • Experience with aseptic fill/finish is preferred.
  • Familiarity with aseptic technique and cleanroom personnel flows is desirable.
  • Knowledge of process flows, including disposables strategies, filtration, mixing strategies, and fluid transfer to and from various vessels, is a plus.
  • Working knowledge of process engineering aids such as sanitary connections, valves, and pharmaceutical process design is desirable.

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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