Production Supervisor - Blending, Encapsulation, and Washroom

IFF•Clackamas, OR

40d•$61,558 - $87,940•Onsite

About The Position

The Production Supervisor – Blending, Encapsulation, and Washroom is responsible for overseeing production operations on assigned production lines during designated shifts. Responsibilities include monitoring the performance of employees and temporary staff, ensuring proper use and care of production equipment, and maintaining facility standards within the assigned area. The role enforces adherence to established manufacturing processes and ensures achievement of production targets while prioritizing safety and quality requirements. Oversight of washroom personnel includes inspection, evaluation, and training activities to ensure compliance with sanitation standards and prevention of product contamination. The position supports cross-functional collaboration with other production departments and site support functions. Additional responsibilities include completion of daily documentation related to team activities and promotion of a continuous improvement culture within the team.

Requirements

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.
A legal right to work in the United States
Must pass a drug screen and a background check in accordance with HWP standards.

Nice To Haves

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
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 Production
Commitment to high ethical standards and integrity
Works well Independently and in a Team setting
Inspires collaborative thinking and team building

Responsibilities

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 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