Biotechnology, Pharmaceuticals, Aesthetics, Medical Devices

Quality Control Chemist I

Johnson, TNOnsiteInternshipPosted 17 days agoVisa sponsorship available

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Required skills

Quality Control
sampling
raw materials
purified water systems
in-process materials
finished products
Environmental Monitoring
analytical testing
laboratory equipment
cGMP

Nice to have

pharmaceutical industry
Microsoft Office Suite
Excel
PowerPoint
basic math skills
basic chemistry skills

Role summary

The Quality Control Chemist I supports quality control laboratory personnel in sampling raw materials, purified water systems, in-process materials, and finished products. This role involves performing various tests, preparing reagents and samples, operating laboratory equipment, and ensuring a safe work environment. The position reports to the QC Supervisor and is based onsite in Johnson City, TN.

Job Summary:

The Quality Control Chemist I performs routine qualitative and quantitative analyses under appropriate supervision to support raw material qualification, in-process monitoring, stability studies, bulk intermediates, and finished product release. The role applies the scientific method and fundamental analytical chemistry skills while developing proficiency in chromatography, laboratory instrumentation, cGMP practices, and accurate documentation.

This entry-level role follows approved procedures, maintains complete and traceable laboratory records, evaluates routine results for accuracy and abnormalities, and promptly communicates issues to supervision. The QC Chemist I supports investigations by providing factual data, participates in 5S and departmental initiatives, and collaborates professionally with Quality Assurance and other functions while continuing to build scientific knowledge and independence.

Reporting to: QC SupervisorLocation: Johnson City, TN – onsiteResponsibilities:

Perform routine testing of raw materials, in-process samples, intermediates, finished products, and stability samples using approved methods and in accordance with cGMP, GDP, and applicable compendial requirements.

Prepare reagents, standards, and sample solutions accurately, with complete documentation and traceability.

Perform wet chemistry analyses and operate chromatographic instrumentation, including HPLC and GC, with appropriate supervision; develop proficiency with non-chromatographic laboratory instruments.

Perform assigned environmental monitoring activities, where applicable, and promptly escalate deviations or unusual results in accordance with procedures.

Record analytical activities and results in laboratory notebooks and electronic systems, such as LIMS, in accordance with GDP and ALCOA+ principles.

Support deviation, OOS, OOT, and laboratory investigations by providing accurate factual data and timely information to the investigator or supervisor.

Follow approved analytical methods and equipment procedures; support method, equipment, or system qualification activities as assigned.

Participate in 5S, laboratory organization, and other continuous improvement activities.

Review own work for accuracy and completeness and seek guidance when results, calculations, or observations are unclear.

Comply with site safety, EHS, PPE, and hazardous-material handling requirements and promptly report safety concerns and near misses.

Maintain laboratory cleanliness, readiness, and compliance with approved procedures and cGMP expectations.

Communicate testing status, issues, and accurate updates to supervision in a timely manner and interact professionally with Quality Assurance and other departments.

Manage assigned tasks and deadlines with supervision, remain open to new initiatives, and complete additional duties or training assigned by QC leadership.

Required Qualifications

Bachelor’s degree (B.S./B.A.) in Chemistry or a related scientific discipline with 1–3 years of relevant laboratory experience; or

Master’s degree in Chemistry or a related scientific discipline with 0–1 year of relevant laboratory experience.

Understanding of the scientific method and experience applying fundamental analytical chemistry principles and laboratory skills.

Ability to follow written procedures accurately and maintain a clear, complete laboratory notebook and accurate data entries in compliance with GDP.

Ability to assess routine situations, propose solutions, recognize the limits of assigned scope, and escalate issues appropriately.

Understanding basic laboratory practices and GLP requirements, with willingness to develop knowledge of cGMP, GDP, ALCOA+, and USP testing expectations.

Clear written and verbal communication skills, including timely reporting of issues and accurate status updates.

Ability to manage one or more assigned tasks with supervision, meet deadlines, adapt to new initiatives, and contribute professionally to the QC team.

Preferred Qualifications

Experience in a regulated pharmaceutical, OTC drug, cosmetic, medical device, or other GMP/GLP laboratory environment.

Familiarity with LIMS or another laboratory information management system.

Basic understanding of chromatographic concepts and experience with HPLC or GC through employment, internship, or academic laboratory work.

Exposure to wet chemistry testing and non-chromatographic laboratory instrumentation.

Awareness of USP testing requirements and experience reviewing analytical data for accuracy, abnormalities, or inconsistencies.

Experience participating in 5S, laboratory organization, or continuous improvement activities.

Company Summary:

Crown is a proud member of the Revance Portfolio of skincare offerings. Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company’s vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance’s award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists. For more information about Revance, please visit us at www.revance.com.What Revance invests in you:

Competitive Compensation including base salary and annual performance bonus.

12 days' PTO, holidays, and parental leave.

Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!

This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a “qualified individual with a disability” in all aspects of the employment relationship. A “qualified individual with a disability” is “an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job.”

Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

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Quality Control Chemist I

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