The Steely Group
Associate Quality Control
The Steely Group, Providence, Rhode Island, United States,
Job Description
Quality Control is searching for an analyst to support routine testing of Raw Materials in the Wet Chemistry laboratory. This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.
The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.
Responsibilities:Performing analytical testing for general chemistry (IDs, LODs, pH, osmolality, appearance, etc.)Interacting cross-functionally with a wide variety of people and teamsTroubleshoot, solve problems and communicate with stakeholdersParticipate in initiatives and projects that may be departmental or organizational in scopeEvaluate lab practices for compliance and operational excellence on a continuous basisRequirements / Qualifications :Bachelor’s degree ORAssociate's degree and 1-2 years of Quality or Analytical Laboratory experience ORHigh school diploma/GED and 3 years of Quality or Analytical Laboratory experienceExperience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracyDemonstrated ability to work independently and deliver right first time resultsExcellent communication skills (written and verbal)Must have focus on data integrityQualified to work in the U.S. without employer sponsorshipCommitment of a 40-hour work week in West Greenwich, RIPreferred Qualifications :1-3 years of experience in GMP analytical laboratoryExperience with bench chemistryExperience with Compendial testingSelf-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervisionStrong communication skills (both written and oral), facilitation and presentation skillsUnderstanding and application of principles, concepts, theories and standards of GMP QC analytical laboratoriesUnderstanding of biopharmaceuticals process and related unit operationsStrong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracyIndependent, self-motivated, organized, able to multi-task in time-sensitive environmentsDemonstrated experience in investigations and QC processes
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Quality Control is searching for an analyst to support routine testing of Raw Materials in the Wet Chemistry laboratory. This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.
The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.
Responsibilities:Performing analytical testing for general chemistry (IDs, LODs, pH, osmolality, appearance, etc.)Interacting cross-functionally with a wide variety of people and teamsTroubleshoot, solve problems and communicate with stakeholdersParticipate in initiatives and projects that may be departmental or organizational in scopeEvaluate lab practices for compliance and operational excellence on a continuous basisRequirements / Qualifications :Bachelor’s degree ORAssociate's degree and 1-2 years of Quality or Analytical Laboratory experience ORHigh school diploma/GED and 3 years of Quality or Analytical Laboratory experienceExperience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracyDemonstrated ability to work independently and deliver right first time resultsExcellent communication skills (written and verbal)Must have focus on data integrityQualified to work in the U.S. without employer sponsorshipCommitment of a 40-hour work week in West Greenwich, RIPreferred Qualifications :1-3 years of experience in GMP analytical laboratoryExperience with bench chemistryExperience with Compendial testingSelf-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervisionStrong communication skills (both written and oral), facilitation and presentation skillsUnderstanding and application of principles, concepts, theories and standards of GMP QC analytical laboratoriesUnderstanding of biopharmaceuticals process and related unit operationsStrong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracyIndependent, self-motivated, organized, able to multi-task in time-sensitive environmentsDemonstrated experience in investigations and QC processes
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