C

Curia

End-to-end drug development and manufacturing

Process Engineer 4

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 and at least eight years of experience in a cGMP/FDA-regulated environment, or a master's degree in Biology, Chemical Engineering, or a related field and at least six years of experience in a cGMP/FDA-regulated environment.
  • Ability to read and interpret safety instructions, standard operating procedures, technical procedures, and governmental regulations.
  • Strong written and verbal communication skills, including presentation skills to present information and respond to questions from groups of managers, clients, customers, and the general public.
  • Proficiency in arithmetic operations across measurement units, including whole numbers, fractions, decimals, and percentages, and a strong grasp of algebraic and geometric principles.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions; interpret technical instructions in mathematical or diagram form and manage abstract and concrete variables.
  • Proficiency using manufacturing and internet software, and Microsoft Office tools including PowerPoint, Excel, Word, and Outlook.
  • Must pass a background check and drug screen.
  • May be required to pass Occupational Health Screening, obtain and maintain gowning certification, obtain and maintain media qualification, and wear a respirator.
  • May need to meet physical requirements including lifting, pushing, pulling, sitting, standing, reaching, and other activities depending on the position; visual acuity and hand and finger dexterity are required.
  • Aseptic gowning and task-dependent personal protective equipment are required in the pharmaceutical manufacturing environment; contact lenses are prohibited in work areas with exposure to cleaning agents.

Responsibilities

  • Develop batch records for client-specific formulation and filling operations.
  • Oversee engineering and GMP processing operations, including equipment preparation, bulk product formulation, sterile filtration, and filling support, to facilitate process design and internal technology transfer.
  • Serve as a subject matter expert for GMP investigations, including CAPA, departures, and CCRs, with senior or managerial engineering support; finalize closure reports for assigned process-engineering departures.
  • Discuss routine matters directly with clients and summarize completed engineering work verbally and in writing, with support from more senior engineers as needed.
  • Identify and specify process-specific equipment for client technology transfers, and develop techniques and process parameters for client products while maintaining critical product attributes.
  • Author equipment operating instructions and document process flows in the cleanroom facility.
  • Develop new manufacturing processes to meet client requirements.
  • Adhere to safety requirements and raise process deviations to the shift supervisor, engineering manager, and/or quality assurance.

Desired Qualifications

  • Experience with aseptic fill/finish.

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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