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Process Engineer II – Albuquerque, NM
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Process Engineer II - Albuquerque, NM
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VetJobs .
ATTENTION MILITARY AFFILIATED JOB SEEKERS
- Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On‑Site" at the location detailed in the job post.
Process Engineer II in Albuquerque, NM Build your future at Curia, where our work has the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.
Benefits
Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!
Summary The Process Engineer II is responsible for facilitating the technology transfer of client processes and executing engineering functions including design, scale‑up, documentation. This role functions as a program lead with direction from the functional group leadership. The Engineer provides guidance and instruction to supporting team members on tasks directly related to their project, in addition to providing training for new team members.
Essential Duties and Responsibilities
Develop batch records and lead process activities for client‑specific formulation and filling operations for at least one client.
Oversee critical operations (ENG and GMP) including equipment preparation, bulk product formulation, sterile filtration, and filling support.
Act as an SME for GMP investigations (CAPA, departures, CCRs) from initiation to closure.
Finalize closure reports for the departures assigned to process engineering.
Conduct direct client interaction for routine discussions, summarizing engineering‑related work completed verbally and in writing. Client communication will be supported by more senior‑level engineers, as needed.
Identify and specify process‑specific equipment based on facility, client, and program needs. Author instructions for the operation of equipment and for detailing 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 operation tasks, such as those captured in SOPs or work instructions.
Provide training on client programs and processes.
Communicate deviations to the appropriate leaders involved in the production process.
Read/interpret SOPs to ensure compliance.
Maintain up‑to‑date trainings.
Perform other duties as assigned.
Additional Qualifications / Responsibilities Bachelor’s degree in Biology, Chemical Engineering, or related field of study.
Minimum of three (3) years’ experience in Pharmaceutical, Biotech or related industry.
Minimum of three (3) years’ experience in process engineering work experience.
Experience with aseptic fill/finish, preferred.
This role does not have supervisory responsibilities, yet it may involve mentoring, guiding, and advising.
Language, Mathematical, and Reasoning Skills
Read and interpret various documents, such as safety instructions, standard operating procedures, technical procedures, and governmental regulations.
Strong written and verbal communication skills, along with effective presentation skills.
Proficient in executing arithmetic operations across various units of measurement, employing whole numbers, fractions, decimals, and percentages.
Strong grasp of algebraic and geometric principles.
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagrammatic form.
Computer Skills The ideal candidate will possess a strong technical foundation and proven capability in effectively utilizing diverse software tools to streamline the organization’s daily functions. Essential skills encompass proficiency in manufacturing and internet software, alongside Microsoft Office tools including PowerPoint, Excel, Word, and Outlook.
Other Skills and Abilities
Provides guidance and mentorship to team members.
Fosters a collaborative and positive work environment.
Champions change.
Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
Demonstrates strong attention to detail.
Ability to work with a moderate amount of supervision; interact well with clientele as well as interdepartmentally.
Strong communication skills, as well as a meticulous and organized approach.
Familiarity with aseptic technique and cleanroom personnel flows desirable.
Knowledge of process flows – Disposable’s strategies, filtration, mixing strategies, fluid transfer to and from various vessels is a plus.
Working knowledge of process engineering processing aids such as sanitary connections, valves, and pharmaceutical process design.
Other Qualifications
Must pass a background check.
Must pass a drug screen.
Must be able to obtain and maintain gowning certification.
May be required to obtain and maintain media qualification.
May be required to wear a respirator.
Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Location and Company Information City: Albuquerque State: New Mexico Job Code: Manufacturing Manufacturing Affiliate Sponsor: Curia
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Process Engineer II - Albuquerque, NM
role at
VetJobs .
ATTENTION MILITARY AFFILIATED JOB SEEKERS
- Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On‑Site" at the location detailed in the job post.
Process Engineer II in Albuquerque, NM Build your future at Curia, where our work has the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.
Benefits
Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!
Summary The Process Engineer II is responsible for facilitating the technology transfer of client processes and executing engineering functions including design, scale‑up, documentation. This role functions as a program lead with direction from the functional group leadership. The Engineer provides guidance and instruction to supporting team members on tasks directly related to their project, in addition to providing training for new team members.
Essential Duties and Responsibilities
Develop batch records and lead process activities for client‑specific formulation and filling operations for at least one client.
Oversee critical operations (ENG and GMP) including equipment preparation, bulk product formulation, sterile filtration, and filling support.
Act as an SME for GMP investigations (CAPA, departures, CCRs) from initiation to closure.
Finalize closure reports for the departures assigned to process engineering.
Conduct direct client interaction for routine discussions, summarizing engineering‑related work completed verbally and in writing. Client communication will be supported by more senior‑level engineers, as needed.
Identify and specify process‑specific equipment based on facility, client, and program needs. Author instructions for the operation of equipment and for detailing 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 operation tasks, such as those captured in SOPs or work instructions.
Provide training on client programs and processes.
Communicate deviations to the appropriate leaders involved in the production process.
Read/interpret SOPs to ensure compliance.
Maintain up‑to‑date trainings.
Perform other duties as assigned.
Additional Qualifications / Responsibilities Bachelor’s degree in Biology, Chemical Engineering, or related field of study.
Minimum of three (3) years’ experience in Pharmaceutical, Biotech or related industry.
Minimum of three (3) years’ experience in process engineering work experience.
Experience with aseptic fill/finish, preferred.
This role does not have supervisory responsibilities, yet it may involve mentoring, guiding, and advising.
Language, Mathematical, and Reasoning Skills
Read and interpret various documents, such as safety instructions, standard operating procedures, technical procedures, and governmental regulations.
Strong written and verbal communication skills, along with effective presentation skills.
Proficient in executing arithmetic operations across various units of measurement, employing whole numbers, fractions, decimals, and percentages.
Strong grasp of algebraic and geometric principles.
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagrammatic form.
Computer Skills The ideal candidate will possess a strong technical foundation and proven capability in effectively utilizing diverse software tools to streamline the organization’s daily functions. Essential skills encompass proficiency in manufacturing and internet software, alongside Microsoft Office tools including PowerPoint, Excel, Word, and Outlook.
Other Skills and Abilities
Provides guidance and mentorship to team members.
Fosters a collaborative and positive work environment.
Champions change.
Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
Demonstrates strong attention to detail.
Ability to work with a moderate amount of supervision; interact well with clientele as well as interdepartmentally.
Strong communication skills, as well as a meticulous and organized approach.
Familiarity with aseptic technique and cleanroom personnel flows desirable.
Knowledge of process flows – Disposable’s strategies, filtration, mixing strategies, fluid transfer to and from various vessels is a plus.
Working knowledge of process engineering processing aids such as sanitary connections, valves, and pharmaceutical process design.
Other Qualifications
Must pass a background check.
Must pass a drug screen.
Must be able to obtain and maintain gowning certification.
May be required to obtain and maintain media qualification.
May be required to wear a respirator.
Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Location and Company Information City: Albuquerque State: New Mexico Job Code: Manufacturing Manufacturing Affiliate Sponsor: Curia
#J-18808-Ljbffr