Charles River Laboratories
Research Analyst I, Formulations
Charles River Laboratories, Ashland, Ohio, United States, 44805
1 day ago Be among the first 25 applicants
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, we’ll help you build a career that you can feel passionate about.
Job Summary We are seeking an experienced
Research Analyst I
for our
Formulations Team
at our Safety Assessment site located in
Ashland, OH .
Basic Summary A Research Analyst I – Formulations will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight.
Essential Duties and Responsibilities
Prepare basic to complex dosing material and samples for solutions, suspensions, diets, and dispensations.
Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.).
Independently sterilize laboratory equipment using autoclave or other methods.
Assist in washing and maintenance of glassware and lab cleanliness.
Assist with the disposal of residual dosing material.
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
Independently identify equipment issues for troubleshooting and notify proper personnel.
Actively participate in process improvement initiatives.
Provide feedback on laboratory investigations and quality observations.
Utilize various mixing methods and apparatuses to prepare formulations.
Prepare aseptic and glovebox formulations with oversight.
Prepare formulations under observation of Study Directors.
Perform all other related duties and functions as assigned.
The pay for this position is $21.00. Salary may vary based on experience, skills, education, certifications, and location.
Job Qualifications
Education & Experience: Bachelor’s degree (B.A./B.S.) in a relevant field with no experience strongly recommended. An equivalent combination of education and experience may be accepted as a satisfactory substitute.
Good written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite). Ability to learn a validated system.
Maintain a safe working environment by observing all safety procedures and using proper protective equipment.
Ensure integrity of studies and regulatory compliance by following GLP, SOPs, BOP, and IACUC rules.
Work extended hours beyond the normal schedule, including evenings, weekends, and shifts with short notice or unscheduled.
Work under specific time constraints.
Physical Demands
Must be able to lift, move, manipulate and/or hold heavy objects up to 50 pounds.
Perform procedures standing or sitting for long periods, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing PPE according to OSHA regulations.
Frequently hold and manipulate work materials while utilizing fine motor skills.
Regularly provide and receive information through various technologies, media, sources, and contacts.
Operate a computer and related office machinery.
Move around the work area to access file cabinets, office machinery, etc.
Maintain vision abilities including close vision, color vision, depth perception, and focus adjustment.
Work Environment
General office and lab conditions; moderate noise level.
Regularly required to wear protective clothing (goggles, face shield, cap, gloves, scrubs, shoe covers) and work near toxic or caustic chemicals and biohazards.
Occasional exposure to live animals, allergens, zoonotic diseases, and biohazards.
Potential exposure to fumes or airborne particles, unpleasant odors, and extreme temperature conditions.
Noise level ranges from moderate to high depending on tasks.
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 productivity and effectiveness, and increases speed to market.
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.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
For agents needing special assistance or an accommodation due to a disability, please contact our Human Resources team by sending an email to
crrecruitment_US@crl.com . 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-Ljbffr
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, we’ll help you build a career that you can feel passionate about.
Job Summary We are seeking an experienced
Research Analyst I
for our
Formulations Team
at our Safety Assessment site located in
Ashland, OH .
Basic Summary A Research Analyst I – Formulations will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight.
Essential Duties and Responsibilities
Prepare basic to complex dosing material and samples for solutions, suspensions, diets, and dispensations.
Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.).
Independently sterilize laboratory equipment using autoclave or other methods.
Assist in washing and maintenance of glassware and lab cleanliness.
Assist with the disposal of residual dosing material.
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
Independently identify equipment issues for troubleshooting and notify proper personnel.
Actively participate in process improvement initiatives.
Provide feedback on laboratory investigations and quality observations.
Utilize various mixing methods and apparatuses to prepare formulations.
Prepare aseptic and glovebox formulations with oversight.
Prepare formulations under observation of Study Directors.
Perform all other related duties and functions as assigned.
The pay for this position is $21.00. Salary may vary based on experience, skills, education, certifications, and location.
Job Qualifications
Education & Experience: Bachelor’s degree (B.A./B.S.) in a relevant field with no experience strongly recommended. An equivalent combination of education and experience may be accepted as a satisfactory substitute.
Good written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite). Ability to learn a validated system.
Maintain a safe working environment by observing all safety procedures and using proper protective equipment.
Ensure integrity of studies and regulatory compliance by following GLP, SOPs, BOP, and IACUC rules.
Work extended hours beyond the normal schedule, including evenings, weekends, and shifts with short notice or unscheduled.
Work under specific time constraints.
Physical Demands
Must be able to lift, move, manipulate and/or hold heavy objects up to 50 pounds.
Perform procedures standing or sitting for long periods, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing PPE according to OSHA regulations.
Frequently hold and manipulate work materials while utilizing fine motor skills.
Regularly provide and receive information through various technologies, media, sources, and contacts.
Operate a computer and related office machinery.
Move around the work area to access file cabinets, office machinery, etc.
Maintain vision abilities including close vision, color vision, depth perception, and focus adjustment.
Work Environment
General office and lab conditions; moderate noise level.
Regularly required to wear protective clothing (goggles, face shield, cap, gloves, scrubs, shoe covers) and work near toxic or caustic chemicals and biohazards.
Occasional exposure to live animals, allergens, zoonotic diseases, and biohazards.
Potential exposure to fumes or airborne particles, unpleasant odors, and extreme temperature conditions.
Noise level ranges from moderate to high depending on tasks.
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 productivity and effectiveness, and increases speed to market.
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.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
For agents needing special assistance or an accommodation due to a disability, please contact our Human Resources team by sending an email to
crrecruitment_US@crl.com . 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-Ljbffr