Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Quality Control Analytical Chemist

Job

Chemence Medical Inc

Alpharetta, GA (In Person)

Full-Time

Posted 3 weeks ago (Updated 6 days ago) • Actively hiring

Expires 7/21/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
54
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Quality Control Analytical Chemist Chemence Medical Inc - 3.2 Alpharetta, GA Job Details Full-time 8 hours ago Benefits Disability insurance Health insurance Dental insurance 401(k) Tuition reimbursement Paid time off Vision insurance 401(k) matching Life insurance Referral program Retirement plan Qualifications Spanish Teamwork Laboratory equipment maintenance English Research Bachelor's degree Equipment maintenance Chemical testing FDA regulations
Full Job Description Summary:
The Quality Control Analytical Chemist ensures that a quality product is produced, following compliance protocols and testing.
Key Duties and Responsibilities:
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Quality Control Analytical Chemist personnel contribute to the company's success by ensuring that quality product is released for sale on the marketplace, that all FDA compliance protocols are followed, arid that the tissue adhesive products tested are analyzed using qualified/validated instrumentation, software, and test procedures. Quality Control Analytical Chemist personnel are responsible for understanding how the chemical and physical analysis of raw materials, intermediate products and final sterilized products adhere to approved test methods, and industry standards and specifications. Duties include but are not limited to technical writing of qualification, validation and study protocols and reports, SOP creation and revision, laboratory investigations, deviation reports and non-conformance reports; research into changing regulations, audit findings, test method updates and advancing technology; laboratory and equipment upkeep; testing of samples; and collaboration with other departments. Other duties assigned. Qualifications, Education and/or
Experience Required:
Requires a 4-year bachelor's degree in chemistry, biochemistry, chemical engineering or related field, and 1-2 years of experience in a QC lab, or chemistry field, preferably in medical device or pharmaceutical environment. Familiarity with analytical testing concepts, practices, instrumentation, and equipment procedures. and maintenance. Preferably has a working knowledge of cGMP and FDA regulations.
Language Skills:
English required; Spanish is a plus. Reasonable accommodations can be made, up to and including translation services.
Physical Demands:
Position requires walking, standing for prolonged periods, occasionally required to sit, climb, or balance, stoop, kneel, crouch or crawl. May frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.
Work Environment:
Analytical Chemistry Laboratory - exposure to chemical solvents like acetone, ethanol, ethyl acetate and tetrahydrofuran. Must follow all lab and company safety procedures and wear proper PPE. Non-temperature-controlled warehouse, non-temperature-controlled production floor, temperature- controlled office.
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
AAP/EEO Statement:
CHEMENCE
® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Job Type:
Full-time Benefits:
401(k) 401(k) matching Dental insurance Disability insurance Health insurance Life insurance Paid time off Referral program Retirement plan Tuition reimbursement Vision insurance Application Question(s): This position is Monday - Friday 8:30 A.M. - 5:30 P.M. are you able to work this shift? Will you now, or in the future, require sponsorship for employment visa status (e.g. H-1B visa status)? What date can you start? What are your salary expectations? Please list a range
Work Location:
In person