Chemist I

IFF•Clackamas, OR

9d•$61,558 - $87,940•Onsite

About The Position

IFF is a global leader in flavors, fragrances, food ingredients, and health and biosciences, delivering sustainable innovations. The Chemist I role is based in Clackamas, Oregon, on the IFF Health & Biosciences team. The position performs routine chemical analyses of dietary supplement materials, including raw materials, in-process samples, and finished products, using approved analytical methods and instrumentation such as HPLC, HPTLC, UV-Vis, GC-FID, and ICP-MS. It supports laboratory operations through sample preparation, analytical testing, accurate recordkeeping, equipment and work-area upkeep, and compliance with established procedures and regulated-laboratory requirements. The role requires close attention to detail, organizational skills, effective workload management, and a willingness to develop technical competency. The Chemist I works under approved methods and procedures, assists with non-conformance investigations and method verification or implementation as assigned, and completes required training, certifications, qualifications, and annual requalifications to support ISO/IEC 17025, AOAC, and cGMP compliance. The stated schedule is 8:00 a.m. to 4:30 p.m., Monday through Friday; business needs may require the position to exceed 40 hours per week.

Requirements

B.S. degree in Chemistry or a related scientific field.
0–2 years of experience in a laboratory environment.
Basic understanding of laboratory techniques and instrumentation.
Familiarity with Good Documentation Practices (GDP).
Ability to follow written procedures and work instructions.
Strong organizational skills and attention to detail.
Some technical writing and problem-solving skills.
Proficiency in Microsoft applications, such as the MS Office Suite.
Effective communication and interpersonal skills.
Legal right to work in the United States.
Ability to pass a drug screen and background check in accordance with IFF standards.
Ability to pass job-related tests and certifications for work in a cGMP quality environment and maintain required annual requalifications.

Nice To Haves

Exposure to ISO/IEC 17025, AOAC, cGMP, or other regulated environments.
Clear focus on high-quality production.
Positive demeanor.
Dependability demonstrated through attendance and job duties.
Interest in continuous improvement, improving processes, and challenging the status quo.

Responsibilities

Perform and accurately document routine chemical analyses of raw materials, in-process samples, and finished products using approved analytical and wet chemistry methods and instrumentation including HPLC, HPTLC, UV-Vis, GC-FID, and ICP-MS.
Use approved methods and proper techniques to analyze chemical compounds and constituents in powder and encapsulated materials.
Prepare samples, reagents, standards, and laboratory solutions in accordance with approved procedures.
Maintain complete and accurate laboratory records, calculations, and supporting documentation to ensure data integrity.
Assist with investigations of non-conformances under the guidance of senior staff or leadership.
Assist with method verifications and implementation of laboratory procedures as assigned.
Maintain laboratory equipment, supplies, and work areas in a clean and organized manner.
Participate in training activities and continue developing technical skills.
Maintain consistent on-site attendance aligned with the assigned work schedule.
Demonstrate sound judgment, attention to detail, and willingness to learn new techniques and responsibilities.
Collaborate effectively and maintain positive working relationships with team members.
Complete and maintain required training, certifications, qualifications, and periodic requalifications for ISO/IEC 17025, AOAC, and cGMP compliance.
Pass and annually requalify on job-related tests and certifications required for work in a cGMP quality environment.
Perform other duties as assigned.