Process Engineer I

Curia • Albuquerque, NM

5d

About The Position

The Process Engineer I facilitates technology transfer of client processes and performs engineering functions including design, scale-up, and documentation. The role serves as a program lead under the direction of functional group leadership and provides guidance and instruction to supporting team members on project-related tasks. Based in Albuquerque, New Mexico, the position supports client-specific formulation and filling operations and involves direct client communication, with support from more senior engineers as needed.

Requirements

• Bachelor’s degree in Biology, Chemical Engineering, or a related field of study.
• Pass a background check and drug screen.
• Be able to obtain and maintain gowning certification.
• May be required to obtain and maintain media qualification.
• May be required to wear a respirator.
• Strong communication skills and a meticulous, organized approach.
• Strong attention to detail.
• Ability to work with a moderate amount of supervision and interact effectively with clients and internal departments.
• Ability to take initiative and understand strategic priorities while executing tasks under direction from internal Curia functions.

Nice To Haves

• Process engineering experience.
• At least two years of experience in the pharmaceutical or biotech industry.
• Experience with aseptic fill/finish.
• Familiarity with aseptic technique and cleanroom personnel flows.
• Knowledge of process flows, including disposables strategies, filtration, mixing strategies, and fluid transfer between vessels.
• Working knowledge of process engineering aids such as sanitary connections, valves, and pharmaceutical process design.

Responsibilities

• Lead batch record and process activities for client-specific formulation and filling operations for at least one client.
• Oversee critical engineering and GMP operations, including equipment preparation, bulk product formulation, sterile filtration, and filling support.
• Serve as a subject matter expert for GMP investigations, including CAPAs, departures, and CCRs, from initiation through closure.
• Communicate directly with clients about routine matters and summarize engineering work verbally and in writing.
• Identify and specify process-specific equipment based on facility, client, and program needs.
• Author equipment operating instructions and documents detailing process flows in the cleanroom facility.
• Develop procedures to meet facility and client requirements.
• Adhere to safety requirements.
• Design and provide training on operational tasks documented in SOPs or work instructions.
• Provide training on client programs and processes.
• Read and interpret SOPs to ensure compliance.
• Maintain current training qualifications.
• Provide guidance and mentorship to team members, foster a collaborative work environment, champion change, and promote workplace safety.
• Perform other duties as assigned.

Benefits

• Generous benefit options, eligible from the first day of employment.
• Paid training, vacation, and holidays; vacation accrual begins on the first day of employment.
• Career advancement opportunities.
• Education reimbursement.
• 401(k) program with matching contributions.
• Learning platform.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level