Research Analyst I - Bioanalytical ChemistryReq ID #: 222094Location:Mattawan, MI, US, 49071For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about.**Job Summary**We are seeking an experienced Research Analyst for our Safety Assessment site located in Mattawan, MI.Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP's and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents.Essential Functions:+ Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)+ Demonstrate effective communication skills through informal discussions with peers, supervisor, and team+ Assist with laboratory maintenance functions+ Independently perform laboratory support functions such as labeling and solution preparations+ Assist with maintaining study specific inventory of consumables with oversight+ Write both study and non-study deviations with minimal oversight+ Actively participate in process improvement initiatives with oversight+ Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area+ Assist in execution of routine sample analysis studies with oversight+ Assist in execution of method validation projects with oversight as needed+ Operate laboratory instruments with complete oversight+ Assist with data analysis in appropriate software for at least one analytical platform**Job Qualifications**Qualifications (Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:+ Minimum of a Bachelors degree (BA/BS) or equivalent experience. No previous work experience required+ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above+ Ability to communicate verbally and in writing at all levels inside and outside the organization.+ Experience with LC/MS/MS required+ Basic familiarity with Microsoft Office Suite+ Computer skills, commensurate with Essential Functions, including the ability to learn a validated system+ Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice+ Ability to work under specific time constraints+ Ability to wear proper PPE for the duration of the shift; which includes and is not limited to the following: Gloves, safety glasses, laboratory coat, cartridge respirator, dust/mist respirator, supplied air respirator, Tyvek suit, sleeve protectors.**The pay for this position is $23.50. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location****About Safety Assessment**Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.**About Charles River**Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.At Charles River, we are passionate about our role in improving the quality of peoples lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.**Equal Employment Opportunity**Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected] . This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.For more information, please visit www.criver.com.#J-18808-Ljbffrby Jobble

Research Analyst I - Analytical Chemistry Req ID #: 222295 Location: Mattawan, MI, US, 49071 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. **Job Summary** The analytical chemistry discipline is responsible for the analysis of dose formulations according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. The team develops and validates methods using a variety of instruments and platforms, with an emphasis on ultra high performance liquid chromatography. The team assures that mixtures of test article with carrier are prepared at the proper concentration, are homogeneous, and are stable. In addition, the team is often involved in investigations and issues that are related to formulations and chemicals used on study. Essential Functions + Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.) + Demonstrate effective communication skills through informal discussions with peers, supervisor, and team + Assist with laboratory maintenance functions + Independently perform laboratory support functions such as labeling and solution preparations + Assist with maintaining study specific inventory of consumables with oversight + Write both study and non-study deviations with minimal oversight + Actively participate in process improvement initiatives with oversight + Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area + Assist in execution of routine sample analysis studies with oversight + Assist in execution of method validation projects with oversight as needed + Operate laboratory instruments with complete oversight + Assist with data analysis in appropriate software for at least one analytical platform + Performs all other related duties as assigned **Job Qualifications** + Minimum of a Bachelors degree (BA/BS) or equivalent experience. No previous work experience required + An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above + Ability to communicate verbally and in writing at all levels inside and outside the organization. + Basic familiarity with Microsoft Office Suite + Computer skills, commensurate with Essential Functions, including the ability to learn a validated system + Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice + Ability to work under specific time constraints Physical Demands: + While performing the duties of this job, the employee must be able to perform general office and/or laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, typing/entering data into a computer, using appropriate instruments, reaching with hands and arms, and wearing safety equipment (PPE) according to OSHA regulations and company standards. + Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus. Work Environment: + General office working conditions, the noise level in the work environment is usually quiet. + While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases. + The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions. The pay range for this position is $23/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. **About Microbial Solutions** Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion. At Charles River, we are passionate about our role in improving the quality of peoples lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019. **Equal Employment Opportunity** Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected] . This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit www.criver.com.

Research Analyst I - Bioanalytical Chemistry Req ID #: 222094 Location: Mattawan, MI, US, 49071 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. **Job Summary** We are seeking an experienced Research Analyst for our Safety Assessment site located in Mattawan, MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP's and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. Essential Functions: + Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.) + Demonstrate effective communication skills through informal discussions with peers, supervisor, and team + Assist with laboratory maintenance functions + Independently perform laboratory support functions such as labeling and solution preparations + Assist with maintaining study specific inventory of consumables with oversight + Write both study and non-study deviations with minimal oversight + Actively participate in process improvement initiatives with oversight + Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area + Assist in execution of routine sample analysis studies with oversight + Assist in execution of method validation projects with oversight as needed + Operate laboratory instruments with complete oversight + Assist with data analysis in appropriate software for at least one analytical platform **Job Qualifications** Qualifications (Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to: + Minimum of a Bachelors degree (BA/BS) or equivalent experience. No previous work experience required + An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above + Ability to communicate verbally and in writing at all levels inside and outside the organization. + Experience with LC/MS/MS required + Basic familiarity with Microsoft Office Suite + Computer skills, commensurate with Essential Functions, including the ability to learn a validated system + Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice + Ability to work under specific time constraints + Ability to wear proper PPE for the duration of the shift; which includes and is not limited to the following: Gloves, safety glasses, laboratory coat, cartridge respirator, dust/mist respirator, supplied air respirator, Tyvek suit, sleeve protectors. **The pay for this position is $23.50. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location** **About Safety Assessment** Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of peoples lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. **Equal Employment Opportunity** Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected] . This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit www.criver.com.

Research Analyst - Bioanalytical Req ID #: 222019 Location: Mattawan, MI, US, 49071 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. **Job Summary** We are seeking a **Research Analyst** for our Bioanalytical Chemistry team at the site located in Mattawan, MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxPs and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. **Essential Functions** (The fundamental competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed: Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.) Demonstrate effective communication skills through informal discussions with peers, supervisor, and team Assist with laboratory maintenance functions Assists with laboratory support functions such as labeling and solution preparations Assist with maintaining study specific inventory of consumables with oversight Independently write both study and non-study deviations Actively participate in process improvement initiatives with minimal oversight Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area Independently execute routine sample analysis studies Execute method validation projects with minimal oversight Independently perform data analysis in appropriate software for at least one analytical platform, while assisting analysis for additional platforms within an operational area Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations Assist with the preparation of paperwork for routine production work with minimal oversight Performs all other related duties as assigned **Job Qualifications** Bachelors degree (BA/BS) or Master's degree. LCMS experience required Ability to communicate verbally and in writing at all levels inside and outside the organization. Basic familiarity with Microsoft Office Suite Computer skills, commensurate with Essential Functions, including the ability to learn a validated system Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice Ability to work under specific time constraints The pay range for this position is $23.50/hr+. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. **About Safety Assessment** Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of peoples lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. **Equal Employment Opportunity** Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected] . This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit www.criver.com.

Research Analyst Jobs in Mattawan, MI

Research Analyst I Bioanalytical Chemistry
April 22, 2024

Research Analyst I Bioanalytical Chemistry
April 21, 2024

Research Analyst I Analytical Chemistry
April 21, 2024

Research Analyst I Bioanalytical Chemistry
April 18, 2024

Research Analyst Bioanalytical
April 11, 2024

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Research Analyst Jobs in Mattawan, MI

Research Analyst I Bioanalytical ChemistryApril 22, 2024

Research Analyst I Bioanalytical ChemistryApril 21, 2024

Research Analyst I Analytical ChemistryApril 21, 2024

Research Analyst I Bioanalytical ChemistryApril 18, 2024

Research Analyst BioanalyticalApril 11, 2024