Senior Process Engineer at Integration International Inc. in Indianapolis, Indiana

Posted in Other 2 days ago.

Type: full-time





Job Description:

Job Details:

Title: Senior Process Engineer

Location: Indianapolis, IN 46221

Duration: 9 Months (Intent to convert at 90 days based on performance)

Work Schedule: 1st Shift, Monday to Friday, 8 AM to 5 PM.

Job Description:

  • The Process Engineer will mentor and support in the diagnoses and resolution of software, instrument, and process problems to maintain system readiness of both manufacturing packaging equipment and the data historian network.
  • You will ensure site compliance and all vital activities are performed on time to keep the equipment in working status.
  • As a member of the Engineering team, you will provide daily support to the Packaging Operations Department with continuous improvement projects, machine solving, and onboarding of assets and new technology.

Core Responsibilities:

  • Identify, define, and action long-term continuous improvement projects through partnership with the site leadership and Operations team.
  • Evaluate process improvements to reduce cost, improve efficiency, and improve quality.
  • Identify, evaluate, and implement process improvement methods for improving worker efficiency, reducing cost, and reducing waste of materials and utilities such as restructuring job duties, reorganizing workflow, relocating workstations and equipment, and purchase of new equipment/technology.
  • Lead multiple project engineering-driven assignments and the associated project schedules, from start to finish with sound project management methodologies.
  • Collaborates with Production to modify workflow barriers and arrangements to increase throughput.

Education/Experience:

  • A Bachelor of Science Degree in Packaging, Mechanical, Industrial, Electrical Engineering, or another scientific subject area from an accredited College or University is required.
  • 5 years of Engineering experience in relevant GMP, pharmaceutical, or food industry required.

Knowledge, Skills, Abilities:

  • Experience with designing, programming, modeling, and testing of automated systems including robotics and clinical packaging equipment to ensure code and configurations meet specifications and validation requirements strongly preferred.
  • Prior experience working within GAMP 5 and GMP environments is strongly desired.
  • Ability to configure process control system software and recipes and collect/format process data to support production or quality department requests.
  • Well-versed in process improvement, and industrial design applications that pertain to a job shop environment.
  • Experience with blister machines, bottling, carding, labeling, and syringe assembly preferred.
  • Must be results-oriented and comfortable training, mentoring, and coaching peers and multi-functional team members.
  • Possesses analytical skills in Lean Manufacturing, Six Sigma, and Single¬ Minute Exchange of Dies (SMED) to enhance quality, reduce rejects, and streamline processes.
  • Experience with failure analysis and reliability engineering preferred.
  • Have strong technical writing skills with experience writing Requirement Specifications (Design, Functional, User), FMEAs, FAT/SAT/Commissioning Protocols, SOPs, and Work Instructions desired.
  • Experience with PLC Automation control system start-ups, loop tuning, solving, and control system modifications is desired.
  • Experience developing sophisticated process control applications applying a mixture of programming formats including sequential function charts, function blocks, and PLC ladder logic preferred.
  • Pharmaceutical experience is required.

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