C

Curia

End-to-end drug development and manufacturing

Process Engineer 2

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.
  • At least three years of experience in the pharmaceutical, biotech, or related industry is required.
  • At least three years of process engineering work experience is required.
  • Candidates must be able to read and interpret safety instructions, standard operating procedures, technical procedures, and governmental regulations.
  • Candidates must demonstrate proficiency with arithmetic operations, units of measurement, algebra, and geometry.
  • Candidates must be able to define problems, collect data, establish facts, draw valid conclusions, and interpret technical instructions in mathematical or diagram form.
  • Candidates must be proficient with manufacturing and internet software and Microsoft Office tools, including PowerPoint, Excel, Word, and Outlook.
  • Candidates must pass a background check and drug screen.
  • Candidates must be able to obtain and maintain gowning certification.
  • Candidates may be required to obtain and maintain media qualification and wear a respirator.

Responsibilities

  • Facilitate technology transfer of client processes and execute engineering functions including design, scale-up, and documentation.
  • Develop batch records and lead process activities for client-specific formulation and filling operations.
  • 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 through closure.
  • Finalize closure reports for departures assigned to process engineering.
  • Interact directly with clients during routine discussions and summarize completed engineering work verbally and in writing.
  • Identify and specify process-specific equipment based on facility, client, and program needs.
  • Author equipment operating instructions and document process flows in the cleanroom facility.
  • Develop new procedures to meet facility and client requirements.
  • Adhere to safety requirements and maintain current training.
  • Design and provide training on operational tasks documented in standard operating procedures or work instructions.
  • Provide training on client programs and processes.
  • Communicate deviations to the appropriate leaders involved in the production process.
  • Read and interpret standard operating procedures to ensure compliance.
  • Provide guidance, mentoring, and advice to team members.
  • Identify and address potential workplace hazards, follow safety protocols, participate in safety training, and promote safety awareness.
  • Work with moderate supervision and coordinate with clients and internal departments to execute task-based work aligned with strategic priorities.
  • Work in office, manufacturing, or warehouse environments as required, including sterile pharmaceutical manufacturing environments requiring aseptic gowning and personal protective equipment.

Desired Qualifications

  • Experience with aseptic fill/finish.
  • Familiarity with aseptic technique and cleanroom personnel flows.
  • Knowledge of process flows, including disposable strategies, filtration, mixing strategies, and fluid transfer to and from vessels.
  • Working knowledge of process engineering aids and pharmaceutical process design, including sanitary connections and valves.

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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