What are the responsibilities and job description for the QC Analyst position at Eastridge?
Eastridge Workforce Solutions is partnering with a leader in developing and manufacturing OTC products for the personal care industry in Totowa, NJ in its search for an Analyst, QC Analytical (OTC) Lab. For immediate consideration, apply today.
Responsibility Summary:
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 products (e.g. Anti-acne, Sanitizers, Sunscreen, etc.) and Cosmetic products.
Responsibilities:
- 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/Skills
- 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
Eastridge Workforce Solutions is an equal opportunity employer and all qualified applicants will receive consideration for employment 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. We celebrate diversity and are committed to creating an inclusive environment for all employees. Please note that Eastridge is unable to provide visa sponsorship to applicants.
Certain clients require Eastridge to perform background checks and Eastridge will consider qualified applicants with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
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