Chemist - Method Development and Validation

Job Description

This position is in-person/on site. This is not a remote position. Must reside in the Phoenix Metro Valley.

Job Type: Full-time, Monday through Friday, Day Shift

Salary: 60 - 70k/yr

Omnient Labs offers a benefits package which includes Medical, Dental, Vision, matching 401(k), employee discounts, PTO and more.

Pre-employment background check mandatory.

Chemist – Method Development and Validation Duties:

Perform method validation, verification, and robustness studies for established HPLC, UPLC, LC MS/MS, HS GC, GC FID, HPTLC, UV Vis, and FTIR methods under the direction of senior method development staff.

Assist with development of lower complexity analytical methods for routine testing, following USP <1225>, USP <1226>, and AOAC Appendix K, with technical review by senior chemists.

Support method transfer activities (e.g., HPLC to UPLC) for routine methods, including preparation of associated documentation and data packages.

Perform method optimization for already developed methods (such as minor adjustments to gradients, injection volumes, sample preparation steps) to improve robustness and efficiency.

Train quality control chemists on validated and transferred methods and provide routine technical support, escalating complex issues to senior chemists.

Execute non routine testing of Research and Development (R&D) materials using established methods and summarize results for senior review.

Analyze samples to determine chemical and/or physical properties, composition, and/or structure utilizing chromatography, spectroscopy, and spectrophotometry according to approved methods.

Maintain a well documented laboratory notebook and ensure all work complies with cGLP and cGMP guidelines.

Participate in daily laboratory functions, calibration activities, hygiene events, and routine laboratory cleaning and maintenance.

Assist with writing and editing laboratory documentation such as standard operating procedures, test methods, or training protocols under direction of laboratory management.

Perform chemical and physical inventory of laboratory supplies, reagents, solvents, and standards on a consistent basis.

Support instrumentation calibration and maintenance schedules to ensure proper condition and calibration of laboratory instrumentation and equipment.

File appropriate paperwork when modifications to laboratory procedures or processes are necessary, such as deviations and change control documentation, with input from senior staff.

Other miscellaneous duties as assigned by laboratory management.

Education/Experience:

A bachelor’s degree in chemistry or chemistry related field, such as biochemistry or molecular biology, is required. A bachelor’s degree in a hard-scientific field such as physics or biology is acceptable. At least 1 year of method development experience (or equivalent) in the food or dietary supplements industry is required.

Technical Skills:

Digital

Proficient using Waters Empower 3 software

Proficient in web-based applications

Analytical

Proficiency with analytical instrumentation such as, HPLC/UPLC, LCMS, specifically Waters UPLC’s

Strong analytical technique and instrumentation skills

Familiar and/or proficient with simple mathematical manipulations and algebra

Meticulous attention to detail, dependability, and excellent organizational skills

Familiarity with analytical instrumentation such as, HSGC, FTIR, UV-Vis HPTLC a plus

Ability to troubleshot and perform maintenance of laboratory instrumentation under the supervision of laboratory management

Interpersonal

Good interpersonal skills, can work proficiently with people of different backgrounds, lifestyles, and values

Team attitude, willing to help others with their tasks and accept help with your tasks

Good communication skills, go out of the way to ensure proper understanding between communicating parties

Working Independently

Able to work independently when necessary

Able to self-manage one’s time for maximum efficiency

Able to complete a long-term project while simultaneously performing multiple smaller, shorter-term projects, or while performing routine QC testing

Full-time