Job Description

Title: Packaging / Process Engineer

Duration: 1 Year Contract

Location: Lake County, IL

Schedule: Monday Friday, 8:00 AM 5:00 PM

Work Model: Onsite initially; optional hybrid (3 days onsite / 2 days remote) once competent

Overtime: Not required but may be needed based on project urgency



TN Visa not acceptable, Visa must be valid for full 12 months duration


Please review the job description below and let me know if you have any suitable consultants available. The candidate must have legitimate work experience and should be available for a video screening.

Top 3 5 Skills

• Strong Technical Background
• Packaging Engineering/Material Science degree preferred
• Initiative/Self Motivated
• Good communication Skills (oral and Written)

Description

Engineering background with experience in:

• Packaging design
• Protocol/report writing
• Understanding of packaging commodity specifications.( Such as Labels, Carton, Leaflets, bottles, Corrugate boxes, ect)
• Define testing parameters and instructions to be executed by Lab Techs.
• Data review and ability to provide conclusions
• Managing projects independently
• Participate in internal/external meetings and lead meetings occasionally
• Work with the Commodities Supplier, if required by the project/task assigned.
• Healthcare/Pharma experience preferred

Responsibilities

• Lead projects in manufacturing process areas to achieve process efficiencies such as increase in process yield, quality improvements, cycle time/throughput, and cost reduction initiatives.
• Gather and analyze process data using statistical process control methodology. Develop action plan to increase process robustness, prevent product loss, and control quality impact. Participate in process performance monitoring such as Track & Trend.
• Responsible for providing technical support in the resolution of shop floor situations and executing assigned tasks as required by the operational area.
• Lead investigations by following a structure problem solving approach and employing sound, scientific principles when identifying root cause and developing recommendations related to product and process. Generate technical justification to support and/or document process deviations/investigations and determine impact in product quality, yield, and product registration.
• Part of cross-functional team responsible for implementation of site projects/initiatives (continuous improvement, cost reduction, capacity increase, etc.) that lead to process remediation.
• Project management of smaller team, short duration projects within larger projects. Responsibility may include project coordination, monitoring, reporting, meeting management, and team communication.
• Lead the implementation of process validation for operational changes, new raw materials, and introduction of new process/technology. Generate technical justification determining impact of change and protocols/reports/manufacturing documents that support its execution. Assist the execution of experimental, demonstration, and validation lots.
• Maintain up-to-date product process documentation and assure they are in compliance with applicable procedures and regulations. Writes justification memos and scientific reports of quality controls and manufacturing documents.
• Provide scientific and technical support during regulatory audits and agency inspections.
• Demonstrate accountability and responsibility for EHS performance and compliance through active participation and support of Abbvie's EHS program.

Qualifications

• BS or MS in Chemistry or Engineering (Chemical, Mechanical, Bio-chemical)
• 3-5 years' of technical experience in Process/Manufacturing/Project Engineering or similar role. Candidates with 2 years of experience on a similar role can be considered.
• Technical knowledge in fundamentals of pharmaceutical solid dosage forms processing.
• Effective verbal and written communication skills.

Key Stakeholders

• Manufacturing, Quality, Supply Chain, Operational Excellence, Engineering, EHS

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