chemist-industrial quality piscataway nj

Job description

Position Overview: Support manufacturing activities by accurately performing analytical chemistry testing (preservative, active ingredients, functional and quasi drugs) in a fast-paced cGMP environment.  Analyze test data and utilize professional judgment to decide on appropriate disposition of material based on specifications and organizational guidelines.

This position would require a weekend shift meaning one weekend day, and you can choose which day you want to work – Saturday or Sunday (can be Tues-Sat OR Sun-Thurs OR Wed-Sun).

Candidates have the option between which weekend shift coverage they prefer. And between 1 st  and 2 nd  shift. We are looking for first, but are open to 2 nd . 1 st  shift starts between 7-9 am plus 8.5 hours, 2 nd  shift starts 1-2 pm.

Key Responsibilities:

·  Supports the Unit of Production (UP) regarding the quality control of raw materials, bulk, WIP, and finished goods.
·  Undertakes all required tests on relevant samples in accordance with L’Oréal specifications, test methods, and USP methods.
·  Carries out relevant preparation, titration, calibration and validation on reagents and/or equipment where appropriate.
·  Good laboratory skills with demonstrated record of excellence in quantitative analysis. Works in compliance with L’Oreal and GMP requirements.
·  Experienced with Root Cause Analysis, ability to troubleshoot out-of-specification results, and perform OOS investigations.
·  Capable of trouble-shooting issues on analytical equipment.
·  Ability to work independently and possesses leadership qualities.
·  Sense of urgency in daily work and towards resolving issues.
·  Ability to make decisions independently and assess when escalation is appropriate.
·  Detail-oriented with a demonstrated proactive and analytical approach to problem solving.
·  Excels at interpersonal communication and able to form effective relationships across departments.
·  Knowledge of standard computer systems such as MS Office (Word, Excel, Outlook); experience using SAP desired.
·  May be asked to lead various quality initiatives or projects.  

Educational or Certification Requirements:

·  Bachelor’s of Science degree required  

Previous Experience:

·  3+ year’s analytical chemistry experience with HPLC, UV-VIS, AA, ICP, GC preferably in cosmetic/consumer products/pharmaceutical manufacturing. Wet chemistry and batch adjustment experience preferred.  

Additional Requirements:

·  Computer skills, to include experience with spreadsheets, presentations, and database management.
·  Experience with SAP a plus.
·  Good knowledge of GMP/ISO or relevant requirements.
·  Strong verbal and written communication skills.

Essential Requirements:

·  Must work well in a fast paced environment and be able to manage multiple priorities simultaneously.
·  Quality/Lab Experience.
·  Analytical and problems solving skills.

We are an Equal Opportunity Employer and take pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.

If you require a reasonable accommodation to complete an application for a recognized disability under applicable law, please email . Please note this email will only respond to specific requests for assistance completing the application as a request for accommodation for a disability. All others will not be considered.","datePosted":"2019-05-19T18:57:28.924000","title":"Chemist-Industrial Quality - Piscataway, Chemist-Industrial Quality - Piscataway, NJ in Piscataway, NJ | Operations at l'oreal       .aurelia-hide { display:none !important; }      L'Oréal | Job Description
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Position Overview: Support manufacturing activities by accurately performing analytical chemistry testing (preservative, active ingredients, functional and quasi drugs) in a fast-paced cGMP environment.  Analyze test data and utilize professional judgment to decide on appropriate disposition of material based on specifications and organizational guidelines.

This position would require a weekend shift meaning one weekend day, and you can choose which day you want to work – Saturday or Sunday (can be Tues-Sat OR Sun-Thurs OR Wed-Sun).

Candidates have the option between which weekend shift coverage they prefer. And between 1 st  and 2 nd  shift. We are looking for first, but are open to 2 nd . 1 st  shift starts between 7-9 am plus 8.5 hours, 2 nd  shift starts 1-2 pm.

Key Responsibilities:

·  Supports the Unit of Production (UP) regarding the quality control of raw materials, bulk, WIP, and finished goods.
·  Undertakes all required tests on relevant samples in accordance with L’Oréal specifications, test methods, and USP methods.
·  Carries out relevant preparation, titration, calibration and validation on reagents and/or equipment where appropriate.
·  Good laboratory skills with demonstrated record of excellence in quantitative analysis. Works in compliance with L’Oreal and GMP requirements.
·  Experienced with Root Cause Analysis, ability to troubleshoot out-of-specification results, and perform OOS investigations.
·  Capable of trouble-shooting issues on analytical equipment.
·  Ability to work independently and possesses leadership qualities.
·  Sense of urgency in daily work and towards resolving issues.
·  Ability to make decisions independently and assess when escalation is appropriate.
·  Detail-oriented with a demonstrated proactive and analytical approach to problem solving.
·  Excels at interpersonal communication and able to form effective relationships across departments.
·  Knowledge of standard computer systems such as MS Office (Word, Excel, Outlook); experience using SAP desired.
·  May be asked to lead various quality initiatives or projects.  

Educational or Certification Requirements:

·  Bachelor’s of Science degree required  

Previous Experience:

·  3+ year’s analytical chemistry experience with HPLC, UV-VIS, AA, ICP, GC preferably in cosmetic/consumer products/pharmaceutical manufacturing. Wet chemistry and batch adjustment experience preferred.  

Additional Requirements:

·  Computer skills, to include experience with spreadsheets, presentations, and database management.
·  Experience with SAP a plus.
·  Good knowledge of GMP/ISO or relevant requirements.
·  Strong verbal and written communication skills.

Essential Requirements:

·  Must work well in a fast paced environment and be able to manage multiple priorities simultaneously.
·  Quality/Lab Experience.
·  Analytical and problems solving skills.

We are an Equal Opportunity Employer and take pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.

If you require a reasonable accommodation to complete an application for a recognized disability under applicable law, please email . Please note this email will only respond to specific requests for assistance completing the application as a request for accommodation for a disability. All others will not be considered.","datePosted":"2019-05-19T18:57:28.924000","title":"Chemist-Industrial Quality - Piscataway, skills, to include experience with spreadsheets, presentations, and database management. 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Position Overview: Support manufacturing activities by accurately performing analytical chemistry testing (preservative, active ingredients, functional and quasi drugs) in a fast-paced cGMP environment.  Analyze test data and utilize professional judgment to decide on appropriate disposition of material based on specifications and organizational guidelines.

This position would require a weekend shift meaning one weekend day, and you can choose which day you want to work – Saturday or Sunday (can be Tues-Sat OR Sun-Thurs OR Wed-Sun).

Candidates have the option between which weekend shift coverage they prefer. And between 1 st  and 2 nd  shift. We are looking for first, but are open to 2 nd . 1 st  shift starts between 7-9 am plus 8.5 hours, 2 nd  shift starts 1-2 pm.

Key Responsibilities:

·  Supports the Unit of Production (UP) regarding the quality control of raw materials, bulk, WIP, and finished goods.
·  Undertakes all required tests on relevant samples in accordance with L’Oréal specifications, test methods, and USP methods.
·  Carries out relevant preparation, titration, calibration and validation on reagents and/or equipment where appropriate.
·  Good laboratory skills with demonstrated record of excellence in quantitative analysis. Works in compliance with L’Oreal and GMP requirements.
·  Experienced with Root Cause Analysis, ability to troubleshoot out-of-specification results, and perform OOS investigations.
·  Capable of trouble-shooting issues on analytical equipment.
·  Ability to work independently and possesses leadership qualities.
·  Sense of urgency in daily work and towards resolving issues.
·  Ability to make decisions independently and assess when escalation is appropriate.
·  Detail-oriented with a demonstrated proactive and analytical approach to problem solving.
·  Excels at interpersonal communication and able to form effective relationships across departments.
·  Knowledge of standard computer systems such as MS Office (Word, Excel, Outlook); experience using SAP desired.
·  May be asked to lead various quality initiatives or projects.  

Educational or Certification Requirements:

·  Bachelor’s of Science degree required  

Previous Experience:

·  3+ year’s analytical chemistry experience with HPLC, UV-VIS, AA, ICP, GC preferably in cosmetic/consumer products/pharmaceutical manufacturing. Wet chemistry and batch adjustment experience preferred.  

Additional Requirements:

·  Computer skills, to include experience with spreadsheets, presentations, and database management.
·  Experience with SAP a plus.
·  Good knowledge of GMP/ISO or relevant requirements.
·  Strong verbal and written communication skills.

Essential Requirements:

·  Must work well in a fast paced environment and be able to manage multiple priorities simultaneously.
·  Quality/Lab Experience.
·  Analytical and problems solving skills.

We are an Equal Opportunity Employer and take pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.

If you require a reasonable accommodation to complete an application for a recognized disability under applicable law, please email . Please note this email will only respond to specific requests for assistance completing the application as a request for accommodation for a disability. All others will not be considered.","locale":"en_GLOBAL","multi_location":[{"cityState":null,"country":"United States","city":"","latlong":{"lon":-74.4663889,"lat":40.5397222},"location":"Piscataway, NJ","lon":"-74.4663889","cityCountry":"United States","cityStateCountry":"United States","state":"","mapQueryLocation":"Piscataway, NJ","stateCountry":"United States","lat":"40.5397222"}],"title":"Chemist-Industrial Quality - Piscataway, NJ","ml_skills_mapping":[{"standardSkill":"Ability to Work Independently","nonStandardSkill":"ability to work independently"},{"standardSkill":"Written Communication Skills","nonStandardSkill":"written communication skills"},{"standardSkill":"Ability to Make Decisions","nonStandardSkill":"ability to make decisions"},{"standardSkill":"Ability to Troubleshoot","nonStandardSkill":"ability to troubleshoot"},{"standardSkill":"Fast Paced Environment","nonStandardSkill":"fast paced environment"},{"standardSkill":"Quantitative Analysis","nonStandardSkill":"quantitative analysis"},{"standardSkill":"Analytical Equipment","nonStandardSkill":"analytical equipment"},{"standardSkill":"Leadership","nonStandardSkill":"leadership qualities"},{"standardSkill":"Analytical Chemistry","nonStandardSkill":"analytical chemistry"},{"standardSkill":"Multiple Priorities","nonStandardSkill":"multiple priorities"},{"standardSkill":"Analytical Approach","nonStandardSkill":"analytical approach"},{"standardSkill":"Database Management System","nonStandardSkill":"database management"},{"standardSkill":"Root Cause Analysis","nonStandardSkill":"root cause analysis"},{"standardSkill":"Computer Systems","nonStandardSkill":"computer systems"},{"standardSkill":"Resolving Issues","nonStandardSkill":"resolving issues"},{"standardSkill":"Sense Of Urgency","nonStandardSkill":"sense of urgency"},{"standardSkill":"Quality Control","nonStandardSkill":"quality control"},{"standardSkill":"Basic Computer Skills","nonStandardSkill":"computer skills"},{"standardSkill":"Detail Oriented","nonStandardSkill":"detail-oriented"},{"standardSkill":"Problem Solving","nonStandardSkill":"problem solving"},{"standardSkill":"Organizational","nonStandardSkill":"organizational"},{"standardSkill":"Raw Materials Management","nonStandardSkill":"raw materials"},{"standardSkill":"Interpersonal Skills","nonStandardSkill":"interpersonal"},{"standardSkill":"Communication Skills","nonStandardSkill":"communication"},{"standardSkill":"Wet Chemistry","nonStandardSkill":"wet chemistry"},{"standardSkill":"Google Sheets","nonStandardSkill":"spreadsheets"},{"standardSkill":"Demonstrated","nonStandardSkill":"demonstrated"},{"standardSkill":"Recruitment","nonStandardSkill":"recruitment"},{"standardSkill":"Reasonable","nonStandardSkill":"reasonable"},{"standardSkill":"Analytical","nonStandardSkill":"analytical"},{"standardSkill":"Validation","nonStandardSkill":"validation"},{"standardSkill":"Leadership","nonStandardSkill":"leadership"},{"standardSkill":"Test Data","nonStandardSkill":"test data"},{"standardSkill":"Proactive","nonStandardSkill":"proactive"},{"standardSkill":"Microsoft Office","nonStandardSkill":"ms office"},{"standardSkill":"Training","nonStandardSkill":"training"},{"standardSkill":"Judgement","nonStandardSkill":"judgment"},{"standardSkill":"Science","nonStandardSkill":"science"},{"standardSkill":"Microsoft Outlook","nonStandardSkill":"outlook"},{"standardSkill":"Testing","nonStandardSkill":"testing"},{"standardSkill":"Veterans Affairs","nonStandardSkill":"veteran"},{"standardSkill":"Ultraviolet Visible Spectroscopy","nonStandardSkill":"uv-vis"},{"standardSkill":"Microsoft Excel","nonStandardSkill":"excels"},{"standardSkill":"Microsoft Excel","nonStandardSkill":"excel"},{"standardSkill":"HPLC","nonStandardSkill":"hplc"},{"standardSkill":"CGMP","nonStandardSkill":"cgmp"},{"standardSkill":"Microsoft Word","nonStandardSkill":"word"},{"standardSkill":"GMP","nonStandardSkill":"gmp"},{"standardSkill":"OOS","nonStandardSkill":"oos"},{"standardSkill":"ICP","nonStandardSkill":"icp"},{"standardSkill":"SAP","nonStandardSkill":"sap"}],"postedDate":"2019-05-19T18:57:28.924000","jobSeqNo":"LOREUS48210","educationRequired":"Bachelor","ml_highlight":"Computer skills, to include experience with spreadsheets, presentations, and database management. Experienced with Root Cause Analysis, ability to troubleshoot out-of-specification results, and perform...","dateCreated":"2019-05-14T13:38:11.695000","ml_role":null,"cityStateCountry":"United States","ml_jobExperience":null,"brands":"R&I","parentRefNum":"LOREUS","ml_skilled_jd":"position overview . support manufacturing activities by accurately performing analytical_chemistry testing preservative, active ingredients, functional and quasi drugs in a fast-paced cgmp environment. analyze test_data and utilize professional judgement to decide on appropriate disposition of material based on specifications and organizational guidelines . this position would require a weekend shift meaning one weekend day, and you can choose which day you want to work – saturday or sunday can be tues-sat or sun-thurs or wed-sun . candidates have the option between which weekend shift coverage they prefer. and between 1st and 2nd shift. we are looking for first, but are open to 2nd. 1st shift starts between 7-9 am plus 8. 5 hours, 2nd shift starts 1-2 pm . key responsibilities . supports the unit of production up regarding the quality_control of raw_materials_management bulk, wip, and finished goods . undertakes all required tests on relevant samples in accordance with l’oréal specifications, test methods, and usp methods . carries out relevant preparation, titration, calibration and validation on reagents and/or equipment where appropriate . good laboratory skills with demonstrated record of excellence in quantitative_analysis works in compliance with l’oreal and gmp requirements . experienced with root_cause_analysis ability_to_troubleshoot out-of-specification results, and perform oos investigations . capable of trouble-shooting issues on analytical_equipment . ability_to_work_independently and possesses leadership . sense_of_urgency in daily work and towards resolving_issues . ability_to_make_decisions independently and assess when escalation is appropriate . detail_oriented with a demonstrated proactive and analytical_approach to problem_solving . microsoft_excel at interpersonal_skills communication_skills and able to form effective relationships across departments . knowledge of standard computer_systems such as microsoft_office microsoft_word microsoft_excel microsoft_outlook . experience using sap desired . may be asked to lead various quality initiatives or projects . educational or certification requirements . bachelor’s of science degree required . previous experience . 3+ year’s analytical_chemistry experience with hplc ultraviolet_visible_spectroscopy aa, icp gc preferably in cosmetic/consumer products/pharmaceutical manufacturing. wet_chemistry and batch adjustment experience preferred . additional requirements . basic_computer_skills to include experience with google_sheets presentations, and database_management_system . experience with sap a plus . good knowledge of gmp iso or relevant requirements . strong verbal and written_communication_skills . essential requirements . must work well in a fast_paced_environment and be able to manage multiple_priorities simultaneously . quality/lab experience . analytical and problems solving skills . we are an equal opportunity employer and take pride in a diverse environment. we do not discriminate in recruitment hiring, training promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veterans_affairs status, medical condition or disability, or any other legally protected status . if you require a reasonable accommodation to complete an application for a recognized disability under applicable law, please email usapplicationaccommodation support.lorealusa.com. please note this email will only respond to specific requests for assistance completing the application as a request for accommodation for a disability. all others will not be considered. ","applyUrl":"//career.loreal.com/careers/login?jobId=63687","ml_filtered_Skills":null,"jobUniqueIdentifierValue":"63687###en_GLOBAL","location":"Piscataway, NJ","cityCountry":"United States","category":"Operations","mapQueryLocation":"Piscataway, NJ","ml_Description":"Position Overview . Support manufacturing activities by accurately performing analytical chemistry testing preservative, active ingredients, functional and quasi drugs in a fast-paced cGMP environment. Analyze test data and utilize professional judgment to decide on appropriate disposition of material based on specifications and organizational guidelines . This position would require a weekend shift meaning one weekend day, and you can choose which day you want to work – Saturday or Sunday can be Tues-Sat OR Sun-Thurs OR Wed-Sun . Candidates have the option between which weekend shift coverage they prefer. And between 1st and 2nd shift. We are looking for first, but are open to 2nd. 1st shift starts between 7-9 am plus 8. 5 hours, 2nd shift starts 1-2 pm . Key Responsibilities . Supports the Unit of Production UP regarding the quality control of raw materials, bulk, WIP, and finished goods . Undertakes all required tests on relevant samples in accordance with L’Oréal specifications, test methods, and USP methods . Carries out relevant preparation, titration, calibration and validation on reagents and/or equipment where appropriate . Good laboratory skills with demonstrated record of excellence in quantitative analysis. Works in compliance with L’Oreal and GMP requirements . Experienced with Root Cause Analysis, ability to troubleshoot out-of-specification results, and perform OOS investigations . Capable of trouble-shooting issues on analytical equipment . Ability to work independently and possesses leadership qualities . Sense of urgency in daily work and towards resolving issues . Ability to make decisions independently and assess when escalation is appropriate . Detail-oriented with a demonstrated proactive and analytical approach to problem solving . Excels at interpersonal communication and able to form effective relationships across departments . Knowledge of standard computer systems such as MS Office Word, Excel, Outlook . experience using SAP desired . May be asked to lead various quality initiatives or projects . Educational or Certification Requirements . Bachelor’s of Science degree required . Previous Experience . 3+ year’s analytical chemistry experience with HPLC, UV-VIS, AA, ICP, GC preferably in cosmetic/consumer products/pharmaceutical manufacturing. Wet chemistry and batch adjustment experience preferred . Additional Requirements . Computer skills, to include experience with spreadsheets, presentations, and database management . Experience with SAP a plus . Good knowledge of GMP/ISO or relevant requirements . Strong verbal and written communication skills . Essential Requirements . Must work well in a fast paced environment and be able to manage multiple priorities simultaneously . Quality/Lab Experience . Analytical and problems solving skills . We are an Equal Opportunity Employer and take pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status . If you require a reasonable accommodation to complete an application for a recognized disability under applicable law, please email USApplicationAccommodation support.lorealusa.com. Please note this email will only respond to specific requests for assistance completing the application as a request for accommodation for a disability. All others will not be considered.