Quality Control Technician II - Raw Materials

IFF•Clackamas, OR

2d•Onsite

About The Position

IFF is a global leader in flavors, fragrances, food ingredients and health & biosciences, delivering sustainable innovations that elevate everyday products. This role is based in Clackamas, OR. The main responsibility of this position is to sample and release incoming raw materials used within the dietary supplement manufacturing process following cGMP guidelines and established procedures. This includes representative sampling of raw materials, internal submission of raw material samples for analysis, and labeling of raw materials. This position works closely with the Material Handler, Purchasing, Quality Assurance, Quality Control, and Production. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.

Requirements

2 years’ experience in a manufacturing environment preferably within quality control
Experience with FDA/cGMP compliance is preferred
Experience with MS Office
Ability to work independently
Requires a well-developed ability to read, write, and speak English in relation to topics of a complex or technical nature
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

A.S. degree in Food science, Biology, or Chemistry preferred

Responsibilities

Review incoming raw and packaging material Certificates-of-Analysis for compliance to purchase specifications.
Sample, quarantine, and label approved raw materials used within the manufacturing process for dietary supplements.
Sample, quarantine, test, label, and release approved packaging materials used within the manufacturing process for dietary supplements.
Utilize and operate a forklift and electric pallet jack within the facility for material movements.
Submit raw material samples for internal and contract laboratory analysis in a timely manner.
Help perform physical characteristics testing of raw materials as needed.
Document any internal non-conformances and out-of-specification conditions.
Communicate any non-conformance issues in a timely fashion to quality leadership.
Support the QC Manager or others during investigations for any non-conformances or customer complaints.
Provide training and guidance as necessary.
Maintain the organization of raw material sample room to adhere to GMPs sanitation and cleanliness.
Perform other duties as assigned.
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.
Re-qualify every year on all job-related tests and certifications as job or qualifications require.