Quality Control Chemist I

Solesence; Romeoville (IL); On-site; USD 60,000 - 65,000; Full time

Job summary

Solésence Beauty Science in Romeoville, IL, seeks a full-time quality control technician with 1+ year lab experience to perform day-to-day QC tasks such as materials inspection, data review, batch file handling, and stability sampling.

You will use ICP-OES, UV/Vis, FTIR, GC, XRF, Viscometer and wet chemistry tools, follow cGMP, and coordinate with production. Some travel to nearby Bolingbrook site is required with travel reimbursement.

Qualifications

• Bachelor’s degree in Chemistry or a technical field.
• cGMP experience preferred (1 year).

Responsibilities

• Tests products for physical and chemical properties at various stages of production processes.
• Inspect production lines and materials, according to quality criteria.
• Perform lab testing related to API, lotions and dispersions.
• Coordinate lab equipment repairs, external calibrations.
• Test and release Lotions & Dispersion within 24 hours of receipt.
• Test and release API (dry) within 48 hours of receipt.
• Compile and evaluate data to determine quality status of in-process, finished goods, and other tests.
• Communicate test results and observations to supervisor and team.

Skills

English communication

Detail oriented

Organized

Team collaboration

Education

Bachelor's degree in Chemistry

cGMP experience

Tools

Salesforce

Rootstock ERP

QuickBase

Dot Compliance

Minitab

MS Word

Excel

Outlook

ICP-OES

UV/Vis

FTIR

GC

XRF

Viscometer

Wet chemistry analysis

Job description

Schedule

8-hour shift, Sunday to Thursday , 10 a m - 7 pm , Overtime expected including some weekends/Holidays

Last Revised

July 2026

ABOUT US

We are a rapidly growing company named Fast Company’s #2 Most Innovative Beauty Company for 2023. Our mission is to enhance lives through healthy skin, partnering with beauty brands to develop and manufacture products that promote skin health for all. We believe the future of sun care is the future of beauty™.

ABOUT THE POSITION

Full-time hourly position that performs day-to-day quality control tasks, including but not limited to, materials inspection and testing, quality data review/management, issuance and review of batch files/labels, reserve/stability samples upkeep, and communication of quality data. The position requires the use of basic, to advanced, quality tools and instruments in a laboratory setting including but not limited to: ICP-OES, UV/Vis, FTIR, GC, XRF, Viscometer, Wet chemistry analysis (1+ years' experience preferred).

Essential Duties and Responsibilities

• Tests products for physical and chemical properties at various stages of production processes. Inspect production lines and materials, according to quality criteria.
• Must be able to perform lab testing related to API (dry and Wet), lotions and dispersions.
• Coordinates lab equipment repairs, external calibrations.
• Must be able to test and release Lotions & Dispersion within 24 hours of receipt.
• Must be able to test and release API (dry) within 48 hours of receipt.
• Compiles and evaluates data generated to determine quality status of in-process, finished goods, and other special tests, as assigned.
• Communicates test results, observations and critical findings to immediate supervisor and other applicable team members. Participates in company team meetings.
• Issues production batch records and labels on a daily basis. Work with production to verify equipment cleanliness.
• Reviews production batch records for accuracy and completeness.
• Supports sampling and preparation of product stability and microbial testing.
• Keeps equipment and laboratory clean, follows assigned safety guidelines and always adheres to assigned company procedures and policies.
• Follows cGMP (current Good Manufacturing Practices), in accordance with provided training. Record and file paperwork and samples according to cGMP requirements.
• Uses simple statistical tools to assist production in process evaluation/troubleshooting.
• Must be able to scan and file documentation, provide support in sample retains and organization of the sample retain system.

Key Character Traits

• Desirous of being an engaged, congenial, and collaborative team member to help achieve mutual success within the department and company.
• High sense of urgency toward meeting or exceeding the expectations of both internal and external stakeholders.
• Thrives within a dynamic environment and easily adapts to changing situations, requirements, and priorities.
• Seeks out opportunities to contribute to the broader organization through collaboratively identifying and solving unmet needs.
• Engages well with people of diverse backgrounds, training, and experience.
• Position is located at Romeoville site but requires periodic travel to Bolingbrook site (within 2 mile radius- travel reimbursement is provided).

Knowledge and Skills

• 0 -2 years of experience in chemical/pharmaceutical industry laboratory.
• 0 - 2 years’ experience with ICP-OES is a plus
• Must be able to learn and execute tasks under company specific software, such as Salesforce, Rootstock ERP, QuickBase, Dot Compliance, Minitab etc.
• Good command of the English language, oral and written.
• Well organized and detail oriented.
• Good verbal and written communication skills.
• Comfortable working with lab scale chemicals (acid based, etc.), as a part of test procedures.
• Proficient in using computers. Good working knowledge of MS Word, Excel, and Outlook.
• Ability to work under pressure and manage multiple projects, meeting tight deadlines.
• Demonstrates flexibility and adaptability to changing priorities and deadlines.

Education/Experience

• Bachelor’s degree in Chemistry, or technical field.
• cGMP: +1 year (Preferred)

PHYSICAL DEMANDS

• Primarily standing work performed in a lab/ manufacturing environment, including extended periods of sitting at a desk and working on a computer.
• Frequent walking and standing required when visiting production areas, attending meetings on the production floor, or engaging with plant personnel.
• Occasional exposure to manufacturing environments, which may include noise, dust, temperature variations, and the need to wear personal protective equipment (PPE).
• Ability to lift and carry materials such as files, laptops, or samples weighing up to 50 pounds.
• Visual and auditory acuity are necessary for reading reports, viewing computer screens, and communicating effectively in person and via digital platforms.
• Manual dexterity for keyboarding, writing, and handling office tools and technology.
• Occasional travel between manufacturing sites or to attend off-site meetings, trainings, or conferences.
• Must be able to work overtime. Possible holidays and weekends on a rotating schedule.
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EQUAL EMPLOYMENT EMPLOYER

Solésence Beauty Science is an Equal Employment Opportunity. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital or parental status, protected veteran status, disability status or any other characteristic protected by law.

Under the Immigration Reform and Control Act (IRCA) of 1986, employers must verify both the identity and employment authorization of every employee. Therefore, employees and applicants must be authorized to work in the United States without the need for sponsorship. While our current hiring plans do not include sponsorship, we remain open to evaluating individual circumstances based on company needs and future opportunities.

Base pay rate for this position is: $29/ hour