Johnson & Johnson companies are equal opportunity employers.
QA Analytical Scientist II-8881140113
Description
Neutrogena Corporation, a member of Johnson & Johnson's Family of Companies, is recruiting for a QA Analytical Scientist II, located in Los Angeles, CA.
Neutrogena Corporation develops, manufactures and markets premium skin and hair care products sold worldwide and recommended by medical professionals. The regulatory classification of the products is principally OTC drug. The product line includes acne treatment products, sun protection, facial care as well as other hair and skin care products.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The QA Analytical Scientist II will perform routine testing to support the Analytical laboratory to ensure achievement of Neutrogena's standards for quality. This individual will comply with Neutrogena's policies, procedures, and quality standards as well as safety and environmental regulations.
Support chemical Raw Material Laboratory activities for use in Neutrogena cGMP production, Responsible for utilizing instrumental and wet chemistry testing including organoleptics, Brookfield viscometer, pH meter, densitometer, UV, potentiometric titrator, Karl Fischer, FT-IR, Conductivity meter, melting point, dropping point, U-Tube viscometers, Sieve Shaker, ICP-MS, Scott Volumeter, Ion Chromatography, TOC Analyzer, HPLC and GC. Ensure the testing and release process for raw materials is in compliance with established specifications, current Good laboratory Practice (cGLP), and all Johnson & Johnson quality assurance requirements. Execute USP method verifications, approved Johnson and Johnson method transfers, and any laboratory-related projects with minimal supervision.
Perform review of analytical chemical testing and organoleptic analysis of materials and products. This individual will generate and perform Laboratory Non-Conformance Reports (NCR) and Laboratory investigations as required. This individual will assist to implement NCR and lab investigation corrective actions to support a compliant laboratory.
This individual will draft protocols, reports, SOPs, and provide feedback on test methods. In addition, this individual will maintain laboratory inventory as needed. This individual will perform appropriate tasks for the laboratory within the quality systems and task, and support the reporting of laboratory metrics. This individual may be qualified to train other employees on troubleshooting, routine analysis, software, quality system, and laboratory processes. This individual will also provide oversight and assist activities of more junior personnel as required by laboratory management.
This individual will perform analytical laboratory projects and investigation under the direction of laboratory management. This individual will assist management to resolve issues pertaining to specialized and detailed analytical laboratory tasks. This candidate must drive process and technical improvements. This individual must collaborate with the team supporting team goals of productivity and compliance. Contribute to technical work in investigations, validation, method verifications, and troubleshooting.
J2W:LI NA
Qualifications
Bachelor's degree in Chemistry or closely related field is required. This position requires a minimum of 5+ years of work experience in a Quality Assurance/QC Analytical laboratory. Knowledge of USP requirements and CFR 211 regulations in the pharmaceutical industry is preferred.
Current experience with a variety of analytical tests of raw materials, in-process materials and finished products is highly preferred. Experience in performing routine and non-routine analytical test methods and USP, ASTM, AOCS, and FCC testing is required. Broad based experience or combination of experience, in analytical testing, test method development, technical transfer, strong science knowledge and understanding of test equipment function is required.
Experience in conducting, executing, and writing laboratory investigations is required. Must have tactical and business knowledge to drive the compliance improvement process. Solid influencing skills to drive process and technical improvements. The ability to drive change and innovation within an analytical lab functional area is required.
Experience writing, modifying, and revising SOPs is required. Fundamental knowledge of regulatory requirements, such as current GMP and GLP regulations is preferred. The ability to review and understand analytical test data is required. Ability to perform and interpret statistical data is required.
Experience with knowledge of calibration and measuring performance of analytical lab testing equipment is highly preferred. Experience with training laboratory personnel is highly preferred. Proficiency with Microsoft Office is required. Experience with LIMS, Empower 2/3, EZ Chrom, Spectrum (UV-VIS), and Chromeleon, is preferred.
This position requires collaboration with management to develop or improve methodologies. This individual will be able to understand process criteria and regulations and business impact of decisions and actions. Strong attention to detail and sense of urgency are also required. Ability to work independently with little guidance is required.
Demonstrates the ability to communicate effectively with management on analytical issues is required.
This position is located in Los Angeles, California and requires the candidate to work professional work schedule. As the business requires, this candidate will need to cover off shifts for the lab.
BE VITAL in your career, Be seen for the talent you bring to work. Explore opportunities within the Johnson & Johnson Family of Companies.
Primary Location:North America-United States-California-Los Angeles
Organization: Neutrogena Corporation (6107)
Job Function: Quality Assurance
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement
QA Analytical Scientist II-8881140113
Description
Neutrogena Corporation, a member of Johnson & Johnson's Family of Companies, is recruiting for a QA Analytical Scientist II, located in Los Angeles, CA.
Neutrogena Corporation develops, manufactures and markets premium skin and hair care products sold worldwide and recommended by medical professionals. The regulatory classification of the products is principally OTC drug. The product line includes acne treatment products, sun protection, facial care as well as other hair and skin care products.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The QA Analytical Scientist II will perform routine testing to support the Analytical laboratory to ensure achievement of Neutrogena's standards for quality. This individual will comply with Neutrogena's policies, procedures, and quality standards as well as safety and environmental regulations.
Support chemical Raw Material Laboratory activities for use in Neutrogena cGMP production, Responsible for utilizing instrumental and wet chemistry testing including organoleptics, Brookfield viscometer, pH meter, densitometer, UV, potentiometric titrator, Karl Fischer, FT-IR, Conductivity meter, melting point, dropping point, U-Tube viscometers, Sieve Shaker, ICP-MS, Scott Volumeter, Ion Chromatography, TOC Analyzer, HPLC and GC. Ensure the testing and release process for raw materials is in compliance with established specifications, current Good laboratory Practice (cGLP), and all Johnson & Johnson quality assurance requirements. Execute USP method verifications, approved Johnson and Johnson method transfers, and any laboratory-related projects with minimal supervision.
Perform review of analytical chemical testing and organoleptic analysis of materials and products. This individual will generate and perform Laboratory Non-Conformance Reports (NCR) and Laboratory investigations as required. This individual will assist to implement NCR and lab investigation corrective actions to support a compliant laboratory.
This individual will draft protocols, reports, SOPs, and provide feedback on test methods. In addition, this individual will maintain laboratory inventory as needed. This individual will perform appropriate tasks for the laboratory within the quality systems and task, and support the reporting of laboratory metrics. This individual may be qualified to train other employees on troubleshooting, routine analysis, software, quality system, and laboratory processes. This individual will also provide oversight and assist activities of more junior personnel as required by laboratory management.
This individual will perform analytical laboratory projects and investigation under the direction of laboratory management. This individual will assist management to resolve issues pertaining to specialized and detailed analytical laboratory tasks. This candidate must drive process and technical improvements. This individual must collaborate with the team supporting team goals of productivity and compliance. Contribute to technical work in investigations, validation, method verifications, and troubleshooting.
J2W:LI NA
Qualifications
Bachelor's degree in Chemistry or closely related field is required. This position requires a minimum of 5+ years of work experience in a Quality Assurance/QC Analytical laboratory. Knowledge of USP requirements and CFR 211 regulations in the pharmaceutical industry is preferred.
Current experience with a variety of analytical tests of raw materials, in-process materials and finished products is highly preferred. Experience in performing routine and non-routine analytical test methods and USP, ASTM, AOCS, and FCC testing is required. Broad based experience or combination of experience, in analytical testing, test method development, technical transfer, strong science knowledge and understanding of test equipment function is required.
Experience in conducting, executing, and writing laboratory investigations is required. Must have tactical and business knowledge to drive the compliance improvement process. Solid influencing skills to drive process and technical improvements. The ability to drive change and innovation within an analytical lab functional area is required.
Experience writing, modifying, and revising SOPs is required. Fundamental knowledge of regulatory requirements, such as current GMP and GLP regulations is preferred. The ability to review and understand analytical test data is required. Ability to perform and interpret statistical data is required.
Experience with knowledge of calibration and measuring performance of analytical lab testing equipment is highly preferred. Experience with training laboratory personnel is highly preferred. Proficiency with Microsoft Office is required. Experience with LIMS, Empower 2/3, EZ Chrom, Spectrum (UV-VIS), and Chromeleon, is preferred.
This position requires collaboration with management to develop or improve methodologies. This individual will be able to understand process criteria and regulations and business impact of decisions and actions. Strong attention to detail and sense of urgency are also required. Ability to work independently with little guidance is required.
Demonstrates the ability to communicate effectively with management on analytical issues is required.
This position is located in Los Angeles, California and requires the candidate to work professional work schedule. As the business requires, this candidate will need to cover off shifts for the lab.
BE VITAL in your career, Be seen for the talent you bring to work. Explore opportunities within the Johnson & Johnson Family of Companies.
Primary Location:North America-United States-California-Los Angeles
Organization: Neutrogena Corporation (6107)
Job Function: Quality Assurance
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement