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    Process Engineer I - Tucson, United States - eTeam

    eTeam
    eTeam Tucson, United States

    4 weeks ago

    eTeam background
    Description

    Job Name:
    Process Engineer I Participates on and leads validations and projects within the manufacturing areas. This engineer is responsible for successful project completion including necessary reports and approvals. Identifies and assists with implementing improvements around current manufacturing processes with guidance from manager and senior engineers. Responsibilities also include equipment and process validations as well as process characterization and root cause investigations. Responsibilities Assess existing processes and equipment and identify and implement improvements. Implement new or transferred manufacturing processes in a timely manner. Lead and/or participate in equipment and process validations. Assist in troubleshooting of process and/or equipment issues. Strong written and verbal communication skills. With guidance, able to prepare and present technical information and project summaries to peers and management. Monitors work to ensure quality and to continuously promote Quality First Time.


    Automation & Factory Support specifics:

    Assist in designing and implementing new equipment and tools to improve manufacturing efficiencies, reduce ergonomic stress, and improve quality.


    • Update, create and sustain Standard Work documents.
    • Create and update drawings using Pro/Engineer or SolidWorks.
    • Work as part of a project team in the development and/or implementation of new equipment and tools.
    • Technical support for daily production issues related to manufacturing equipment.

    Quality Support specifics:

    • Assist in addressing, owning, and resolving quality related issues for the manufacturing departments (ex CAPAs, and Audits)
    • Consistently uses company concepts, policies and procedures, familiar with and follows standard practices.
    • Executes experiments; participates in experimental design.
    • Utilizes DOE where appropriate.
    • Analyzes data, evaluates results, forms conclusions and provides/implements process or document improvements.
    May perform other duties as required or assigned. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities. Formal Training/Education Education Level Education Details Bachelor's Degree BS degree or equivalent in a directly related discipline
    • REQUIRED Experience Years of Experience Experience Details 4 years related experience with BS
    • REQUIRED OR MS degree in directly related discipline + 2 years of related experience required; PhD in directly related discipline and no experience required. Are equivalencies acceptable? No Knowledge, Skills and Abilities Must have the ability to manage priorities based on the needs of the manufacturing area with some guidance from the reporting manager and senior management. Knowledge of biomedical/biotechnology manufacturing. Demonstrates potential for technical proficiency, engineering creativity, collaboration with others, and independent thought. Strong understanding of engineering principles and concepts. Strong computing skills utilizing Microsoft Office tools such as Excel, Word, and Powerpoint Strong teamwork skills. Demonstrated troubleshooting and problem solving skills including the use of designed experiments. Ability to meet project deadlines. Ability to multitask and prioritize with some guidance from management.

    Automation & Factory Support specifics:

    • Experience with automated manufacturing equipment and automation technologies.
    • Experience with CAD programs such as Pro/Engineer and/or SolidWorks.
    • Experience in a regulated environment.
    Knowledge of FDA Quality System Regulations (QSRs) is a plus.
    • Experience with Lean Systems.

    Quality Support specifics:

    • Experience in reagent or instrument manufacturing for a Medical Device or Pharmaceutical company.
    • Experience in a regulated environment.
    Knowledge of FDA Quality System Regulations (QSRs).
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