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Production Supervisor - Blending, Encapsulation, and Washroom

Job in Beaverton, Washington County, Oregon, 97003, USA
Listing for: International Flavors and Fragrances
Full Time position
Listed on 2026-11-01
Job specializations:
  • Manufacturing / Production
    Production QC/QA, Manufacturing & Industrial Operations, Production Manager
Salary/Wage Range or Industry Benchmark: 62000 - 88000 USD Yearly USD 62000.00 88000.00 YEAR
Job Description & How to Apply Below
Job Summary

IFF is a global leader in flavors, fragrances, food ingredients and health & biosciences. We deliver sustainable innovations that elevate everyday products. The IFF-Clackamas site believes that each employee makes a significant contribution to our success. That contribution should not be limited by the assigned responsibilities. Therefore, this position description is designed to outline primary duties, qualifications, and job scope, but not limit the individual nor the organization to just the work identified.

It is our expectation that each employee will offer his/her services wherever and whenever necessary to ensure the success of our endeavors.

WHERE YOU'LL MAKE A DIFFERENCE

SHIFT 2pm - 10:30pm, Monday - Friday

Please note that this is an Exempt/Salaried position that supports a 24/5 plant, this could exceed 40 hours per business needs

  • Perform supervisory functions with a cGMP dietary supplement manufacturing environment per established procedures.
  • Monitor proper stock levels for expendable supplies and components used within the manufacturing process.
  • Responsible for documenting employee activities in terms of performance, corrective action, and attendance.
  • Review and sign off work orders (e.g. cleanings, set-up, beginning of runs, ends of runs, etc....)
  • Review batch records and associated documentation for completeness, legibility, and correctness.
  • Work with quality control to effectively identify, document, and help resolve quality and production issues as needed.
  • Accurately document any out of specification conditions per established procedures.
  • Accurately track work orders internally during the production process.
  • Monitor and verify completeness of all logs for accuracy, completeness, and legibility.
  • Monitor and communicate any changes to production orders including quantities or changes in schedule.
  • Constantly monitor their production environment for compliance to cGMP requirements.
  • Continually assess safety and ensure production employees are working in a safe environment.
  • Report and monitor any unsafe condition.
  • Punctual and Consistent Attendance
  • Support their team to achieve the objectives of the shift.
  • Monitor and support all training activities with their team.
  • Identify and leads in continuous improvement initiatives in their area
  • Complete and verify documentation with accuracy
  • Ability to be at the physical location of the job at the designated shift assigned.
  • Will be asked to train someone and/or participate in a task force to improve company procedures or operations.
  • Ability to be at the physical location of the job for the designated work schedule
  • Will be asked to train someone and/or participate in a task force to improve company procedures or operations.
  • Ability to effectively problem-solve
  • Ability to work collaboratively and maintain effective working relationships with co-workers.
  • Must be able to successfully pass all job-related tests and certifications required for working in a cGMP, quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job. Must re-qualify every year on all job-related tests and certifications as job or qualifications require.
  • Performs other duties as assigned
WHAT MAKES YOU THE RIGHT FIT
  • College Degree OR 5 years' experience in a supervisory role in a manufacturing environment in lieu of degree
  • Computer skills including experience with Microsoft Office and ERP systems
  • Highly organized and detail oriented.
  • Ability to work in a fast paced, results oriented environment.
  • Ability to read and write & communicate in English.
  • Experience with FDA/cGMP compliance is preferred
  • Familiar with Microsoft applications such as MS Office
  • Excellent communication and interpersonal skills with proven ability to take initiative and build strong productive relationships
  • Strong organizational and multi-tasking abilities
  • A legal right to work in the United States
  • Must pass a drug screen and a background check in accordance with HWP standards.
HOW WOULD YOU STAND OUT
  • Possess ability to quickly identify deficiencies and implement corrective action
  • Ability to work well both independently and within a close knit team environment
  • Good communication, interpersonal and customer service skills. Able to effectively communicate with all levels of management and functional areas.
  • Positive Demeanor
  • Dependable, exemplifying this through attendance and job duties
  • Constantly seeking better processes and challenging status quo:
    Continuous Improvement
  • Clear focus on High Quality…
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