Johnson & Johnson companies are equal opportunity employers.
QA SCIENTIST III - 2nd SHIFT-9300140430
Description
Neutrogena Corporation, a member of Johnson & Johnson's Family of Companies, is recruiting for a QA Analytical Laboratory Scientist III – 2nd Shift, 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. 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.
In a team setting and cGMP environment, the QA Scientist III, under routine supervision, performs the physical and chemical testing of raw materials, materials in-process, and finished products to assess conformance to applicable standards.
The Scientist III is primarily responsible for the implementation and management of appropriate testing of raw materials, bulk, and finished goods manufactured at the Neutrogena’s Los Angeles Plant. The Scientist III will ensure the commercial laboratory testing process is well defined, adheres to current Good manufacturing Practices (cGMP)
The Scientist III will ensure all analyst and equipment are appropriately qualified for analytical testing in a cGMP environment. The Scientist III will ensure documents are reviewed for correctness, clarity and conformity to test methods as written.
The position will prepare and standardize test/volumetric solutions, standard solutions and samples for various chemical and physical test according to approved methods, perform and lead others in performing complex analyses including, but not limited to HPLC, GC UV Spectrophotometry, FTIR, and Karl Fischer and prepare data documentation. Key responsibilities include peer review, evaluate and investigate results from various analyses and accountable for identifying trends and reoccurring issues. The Scientists II will prepare, organize and final review paperwork and lab results for lot release to ensure accuracy and completeness, represent the team as a leader in problem solving, troubleshooting and documentation related to laboratory investigations.
The Scientist III is responsible for scientific leadership within the Analytical QA laboratory performing method verification, troubleshooting, and USP method verification. The Scientist III will suggest alternative methods, processes and procedures in solving problems and meeting changing laboratory opportunities. He/she will review technical problems and procedures within the laboratory and recommend solutions to problems or changes in procedures. This individual will comply with Neutrogena’s policies, procedures, quality standards as well as safety and environmental regulations. This individual will assure compliance with all US (e.g. FDA Guidelines, USP, cGMP) and compliance requirements (cGMP and Quality Systems).
This individual will perform more advanced analytical laboratory testing projects and investigation under the direction of the laboratory leadership. This individual assists management as a professional advisor and authoritative figure on issues pertaining to specialized and detailed analytical chemistry tasks.
To perform this job successfully, an individual must be able to perform each Major duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The position will also in involve the following responsibilities in addition to any additional tasks as assigned by the manager:
Comply with J&J/Neutrogena’s policies, procedures, and quality standards, as well as safety and environmental regulations. Perform multiple analytical tests including wet chemistry techniques. Performs laboratory testing of raw materials and finished products for conformity to specification using standard operating procedures. Determines the acceptability of a product or raw material based on test data and test specifications. Assists the laboratory supervisor with laboratory investigations by drafting reports and performing investigational testing. Lead and facilitate improvement projects and initiatives in the laboratory identified continuous improvement initiatives. Confers with Laboratory management on various problems and works in conjunction to develop or improve methodology. Prepare, revise, and implement SOP’s related to the Analytical and Raw Material laboratory in order to maintain compliant with GLP and current regulatory expectations. Assure all compliance issues pertaining to Analytical and Raw material laboratory operations are properly investigated and that corrective actions are devised to prevent recurrence. Performs more advanced analytical testing projects and investigation under the direction of the Analytical and Raw material Laboratory leadership.
Provide technical expertise to colleagues regarding the interpretation and/or implementation of analytical matters. Provide scientific, routine and non-routine technical support for test method transfers, method development, and compendia review. Document all findings appropriately. Prepare and present written and verbal reports to upper management pertaining to analytical technical aspects as required. Assures that instruments used in the test methods are calibrated, maintained and operating properly. Ensures appropriate qualification of laboratory equipment and instruments. Support equipment calibration, preventative maintenance, and service plans. Troubleshoots laboratory equipment and methodologies. Confers with management on various problems and works in conjunction to develop or improve methodology. Assures that standards and reagents used in test methods have been properly labeled, meet quality control standards, are stored in a controlled environment, are within expiry date, and are prepared properly. Conducts training of new colleagues in the areas of new hire orientation to the laboratory, documentation practices, GC, LC, and PQ practices. Provides training in quality systems and task training. Documents training as required.
Evaluates new and existing documentation for test methods. Responsible for working with appropriate R&D groups in developing, validating and recommending changes if needed. Modifies and refines changes in accordance with change control procedures. Reviews and validates test results and makes approve/reject decisions for routine samples. Leads and conducts laboratory investigations in conjunction with the laboratory team leader, consulting with others as needed. This includes developing investigative protocols and evaluating and documenting results. Responsible for maintaining laboratory inventory to ensure that that lab supplies, reagents, and standards are ordered as required supporting laboratory operations. Embraces and demonstrates Johnson & Johnson leadership competencies on an ongoing basis. Ensure implementation and review of service level and quality agreements as appropriate. Implement continuous mitigation and improvement programs within the Analytical and Raw Material Laboratories. Adheres to regulatory, Johnson & Johnson and departmental requirements.
This position will maintain a minimum of 25% bench work.
Qualifications
Bachelor's degree in Chemistry or closely related field is required from a four-year college or university; or equivalent combination of education and experience.
The following experience is required: 6+ years of related work experience in a Quality Assurance/QC Analytical Laboratory, including: 1) Experience in Analytical and West Chemistry testing in a pharmaceutical, OTC, or cosmetic laboratory, 2)Experience in a quality assurance environment preferred, 3)Knowledge of USP regulations in the pharmaceutical industry.
Experience with current Good Laboratory Practices (GLPs) and current Good Manufacturing Practices (cGMPs) is required.
Experience in a GLP/GMP FDA regulated facility manufacturing consumer or pharmaceutical products is required.
Experience in conducting, executing, and leading laboratory investigations is required.
This position is located in Los Angeles and requires negligible travel. The position is on 2nd shift and hours consist of 2:00 – 10:30 pm. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
BE VITAL in your career. Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies!
J2W:LI NA
Primary Location:North America-United States-California-Los Angeles
Organization: Neutrogena Corporation (6107)
Job Function: Quality Control
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 SCIENTIST III - 2nd SHIFT-9300140430
Description
Neutrogena Corporation, a member of Johnson & Johnson's Family of Companies, is recruiting for a QA Analytical Laboratory Scientist III – 2nd Shift, 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. 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.
In a team setting and cGMP environment, the QA Scientist III, under routine supervision, performs the physical and chemical testing of raw materials, materials in-process, and finished products to assess conformance to applicable standards.
The Scientist III is primarily responsible for the implementation and management of appropriate testing of raw materials, bulk, and finished goods manufactured at the Neutrogena’s Los Angeles Plant. The Scientist III will ensure the commercial laboratory testing process is well defined, adheres to current Good manufacturing Practices (cGMP)
The Scientist III will ensure all analyst and equipment are appropriately qualified for analytical testing in a cGMP environment. The Scientist III will ensure documents are reviewed for correctness, clarity and conformity to test methods as written.
The position will prepare and standardize test/volumetric solutions, standard solutions and samples for various chemical and physical test according to approved methods, perform and lead others in performing complex analyses including, but not limited to HPLC, GC UV Spectrophotometry, FTIR, and Karl Fischer and prepare data documentation. Key responsibilities include peer review, evaluate and investigate results from various analyses and accountable for identifying trends and reoccurring issues. The Scientists II will prepare, organize and final review paperwork and lab results for lot release to ensure accuracy and completeness, represent the team as a leader in problem solving, troubleshooting and documentation related to laboratory investigations.
The Scientist III is responsible for scientific leadership within the Analytical QA laboratory performing method verification, troubleshooting, and USP method verification. The Scientist III will suggest alternative methods, processes and procedures in solving problems and meeting changing laboratory opportunities. He/she will review technical problems and procedures within the laboratory and recommend solutions to problems or changes in procedures. This individual will comply with Neutrogena’s policies, procedures, quality standards as well as safety and environmental regulations. This individual will assure compliance with all US (e.g. FDA Guidelines, USP, cGMP) and compliance requirements (cGMP and Quality Systems).
This individual will perform more advanced analytical laboratory testing projects and investigation under the direction of the laboratory leadership. This individual assists management as a professional advisor and authoritative figure on issues pertaining to specialized and detailed analytical chemistry tasks.
To perform this job successfully, an individual must be able to perform each Major duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The position will also in involve the following responsibilities in addition to any additional tasks as assigned by the manager:
Comply with J&J/Neutrogena’s policies, procedures, and quality standards, as well as safety and environmental regulations. Perform multiple analytical tests including wet chemistry techniques. Performs laboratory testing of raw materials and finished products for conformity to specification using standard operating procedures. Determines the acceptability of a product or raw material based on test data and test specifications. Assists the laboratory supervisor with laboratory investigations by drafting reports and performing investigational testing. Lead and facilitate improvement projects and initiatives in the laboratory identified continuous improvement initiatives. Confers with Laboratory management on various problems and works in conjunction to develop or improve methodology. Prepare, revise, and implement SOP’s related to the Analytical and Raw Material laboratory in order to maintain compliant with GLP and current regulatory expectations. Assure all compliance issues pertaining to Analytical and Raw material laboratory operations are properly investigated and that corrective actions are devised to prevent recurrence. Performs more advanced analytical testing projects and investigation under the direction of the Analytical and Raw material Laboratory leadership.
Provide technical expertise to colleagues regarding the interpretation and/or implementation of analytical matters. Provide scientific, routine and non-routine technical support for test method transfers, method development, and compendia review. Document all findings appropriately. Prepare and present written and verbal reports to upper management pertaining to analytical technical aspects as required. Assures that instruments used in the test methods are calibrated, maintained and operating properly. Ensures appropriate qualification of laboratory equipment and instruments. Support equipment calibration, preventative maintenance, and service plans. Troubleshoots laboratory equipment and methodologies. Confers with management on various problems and works in conjunction to develop or improve methodology. Assures that standards and reagents used in test methods have been properly labeled, meet quality control standards, are stored in a controlled environment, are within expiry date, and are prepared properly. Conducts training of new colleagues in the areas of new hire orientation to the laboratory, documentation practices, GC, LC, and PQ practices. Provides training in quality systems and task training. Documents training as required.
Evaluates new and existing documentation for test methods. Responsible for working with appropriate R&D groups in developing, validating and recommending changes if needed. Modifies and refines changes in accordance with change control procedures. Reviews and validates test results and makes approve/reject decisions for routine samples. Leads and conducts laboratory investigations in conjunction with the laboratory team leader, consulting with others as needed. This includes developing investigative protocols and evaluating and documenting results. Responsible for maintaining laboratory inventory to ensure that that lab supplies, reagents, and standards are ordered as required supporting laboratory operations. Embraces and demonstrates Johnson & Johnson leadership competencies on an ongoing basis. Ensure implementation and review of service level and quality agreements as appropriate. Implement continuous mitigation and improvement programs within the Analytical and Raw Material Laboratories. Adheres to regulatory, Johnson & Johnson and departmental requirements.
This position will maintain a minimum of 25% bench work.
Qualifications
Bachelor's degree in Chemistry or closely related field is required from a four-year college or university; or equivalent combination of education and experience.
The following experience is required: 6+ years of related work experience in a Quality Assurance/QC Analytical Laboratory, including: 1) Experience in Analytical and West Chemistry testing in a pharmaceutical, OTC, or cosmetic laboratory, 2)Experience in a quality assurance environment preferred, 3)Knowledge of USP regulations in the pharmaceutical industry.
Experience with current Good Laboratory Practices (GLPs) and current Good Manufacturing Practices (cGMPs) is required.
Experience in a GLP/GMP FDA regulated facility manufacturing consumer or pharmaceutical products is required.
Experience in conducting, executing, and leading laboratory investigations is required.
This position is located in Los Angeles and requires negligible travel. The position is on 2nd shift and hours consist of 2:00 – 10:30 pm. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
BE VITAL in your career. Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies!
J2W:LI NA
Primary Location:North America-United States-California-Los Angeles
Organization: Neutrogena Corporation (6107)
Job Function: Quality Control
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