Formulations Technician I

Req ID #:  203992
Location: 

Horsham, PA, US, 19044

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.

 

IMPORTANT:   In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process.  Please make sure work history and education are added correctly.   


 

Job Summary

Full Time - Day Shift - $750 SIGN ON BONUS

BASIC SUMMARY: 
Prepare article/substance dosage solutions/suspensions according to client specifications for use in toxicology studies.
 
ESSENTIAL DUTIES AND RESPONSIBILITIES: 
•    Perform preparation of test article/substance dosage solution/suspension(s), ensure preparation procedures and calculations are standardized, performed consistently and recorded correctly by the technical personnel.
•    Prepare labels and samples.
•    Receive all incoming test articles/substances and reagents.
•    Ensure that the documentation for the use of all test articles/substances and vehicles/reagents to ensure consistency and correctness.
•    Responsible for the sampling and the shipment of the samples.
•    Maintain cleanliness and general appearance of the Formulations Laboratory.
•    Ensure that test article/substance(s) from completed studies are returned to the sponsor or reassigned to another protocol.
•    Responds to Quality Assurance audits of preparation procedures and calculations.
•    Ensure all chemistry data is submitted to Senior Scientist for weekly review.
•    Maintain an up to day inventory of reagents, test article/substance, vehicles and samples.
•    Review chemistry data on a daily basis and finalizing chemistry data for submission at completion of study.
•    Prepare accurate packing list for the shipment of test article/substances and samples to the sponsor and/or analytical laboratory.  Notify appropriate personnel of shipments.
•    Perform other duties as assigned by supervisor.
 

Job Qualifications

  • QUALIFICATIONS:
    •    Education:  Bachelor’ degree (B.S.) or equivalent 
    •    Experience:   Minimum of 0 to 2 years experience.
    •    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
    •    Certification/Licensure: None.
    •    Other:  Working knowledge of GMP/GLP's a preferred.  GLP environment requires attention to detail strong organizational skills and accurate record keeping competencies.
     

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. 
 

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 120 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 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s 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 people’s 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 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.


Nearest Major Market: Philadelphia

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