Englewood LAB
[Quality Control]
2024-9-18
대기업/중견기업
포지션코드: 228
QC Analytical Chemist
설립일
7/12/2024
직원수
160
고용인원
1
급여
$18 / hr
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Position Information
Position Title
Quality Control
Stipend
$18 / hr
General Responsibilities
The QC Analyst will be responsible for performing material and product testing using approved Methods and Official Compendia. Training and qualifying on Englewood Lab Test Methods. Conducting analytical testing of raw materials, stability samples, bulk and finished products in compliance with all regulatory standards for OTC products (e.g. Anti-acne, Sanitizers, Sunscreen, etc.) and Cosmetic products.
• Review daily instrument calibration and verifications; and review of logbooks.
• Review testing with other analysts and supervisor.
• Perform calibration and system suitability using approved Methods.
• Problem solve with colleagues regarding OOS results, discuss additional testing, operation of equipment, meeting to share ideas. CAPA responsibility.
• Review NCRs prior to submission to Lab Manager, check calculations, possible cause with review of batch records.
• Assist with quality and environmental health and safety audits.
• Perform analytical testing using HPLC, GC, ICP-OES, UV-VIS, Karl Fischer, etc.
• Compliance to Data Integrity requirements.
• Assist with investigation of quality issues such Out of Specification (OOS), Out of Trends (OOT), etc.
• Train on and support the chemical hygiene program for the laboratory.
• Execute testing methods, protocols and other work instructions.
• Assist in managing of chemical and consumable stocks.
• Perform calibrations and system suitability under supervision.
• Familiar with USP/NF Compendia, ASTM, ISO Stds.
• Familiarity with US FDA 21CFR Part 210 & 211 (Drug Product) and Cosmetic GMPs is mandatory.
• Other duties as assigned by manager.
• Review daily instrument calibration and verifications; and review of logbooks.
• Review testing with other analysts and supervisor.
• Perform calibration and system suitability using approved Methods.
• Problem solve with colleagues regarding OOS results, discuss additional testing, operation of equipment, meeting to share ideas. CAPA responsibility.
• Review NCRs prior to submission to Lab Manager, check calculations, possible cause with review of batch records.
• Assist with quality and environmental health and safety audits.
• Perform analytical testing using HPLC, GC, ICP-OES, UV-VIS, Karl Fischer, etc.
• Compliance to Data Integrity requirements.
• Assist with investigation of quality issues such Out of Specification (OOS), Out of Trends (OOT), etc.
• Train on and support the chemical hygiene program for the laboratory.
• Execute testing methods, protocols and other work instructions.
• Assist in managing of chemical and consumable stocks.
• Perform calibrations and system suitability under supervision.
• Familiar with USP/NF Compendia, ASTM, ISO Stds.
• Familiarity with US FDA 21CFR Part 210 & 211 (Drug Product) and Cosmetic GMPs is mandatory.
• Other duties as assigned by manager.
Qualifications
• Bachelor’s degree in Chemistry or related field
• Strong knowledge in GMP, GLP, Root Cause Analysis & Corrective Action Planning Tools
• Laboratory management experience preferred, with experience in Cosmetic or
• Pharmaceuticals desired
• 1+ years Quality Control Analytical Lab experience with HPLC, GC, ICP-OES, UV-VIS, Karl Fischer,
etc.
• Good interpersonal and written communication
• Flexible, ability to multitask and designate
• Good organizational skills
• Strong knowledge in GMP, GLP, Root Cause Analysis & Corrective Action Planning Tools
• Laboratory management experience preferred, with experience in Cosmetic or
• Pharmaceuticals desired
• 1+ years Quality Control Analytical Lab experience with HPLC, GC, ICP-OES, UV-VIS, Karl Fischer,
etc.
• Good interpersonal and written communication
• Flexible, ability to multitask and designate
• Good organizational skills
Working Day
5 Daysdays
Working Hour
9 A.M. to 6 P.M.hour
Employment Visa Type
J-1
Benefit
Accommodations Provided
No
Lunch Provided
No
Overtime Pay
hourly pay rate x 1.5 x overtime hours with prior authorization.
추가혜택/베네핏
N/A
Company Keyword
대기업/중견기업