Are you passionate about medical research and want to make a difference in people's lives?
You are in the right place!
For more than 70 years, Charles River employees have worked together to help discover, develop and safely manufacture new drug therapies. When you join our family, you have a significant impact on the health and well-being of people around the world. Whether your background is in life sciences, finance, computer science, sales or another field, your skills will play an important role in the work we do. In return, we will help you build a career that you can feel passionate about.
We are currently looking for a Chemistry Data Reviewer that will verify data for accuracy, completeness and compliance to Good Laboratory Practice (GLP). Promote awareness of best practices related to data collection.
MAJOR ELEMENTS OF RESPONSIBILITIES
Ensure accuracy and completeness of all raw data, data sets, data transcriptions, generated results, report tables and reports prior to QA submissions;
Verify and review the results generated and/or data integration results generated by Elisa and related techniques, flow cytometry, cell-based assays, molecular biology techniques ;
Verify and review the study specific procedure and the validation study plan before the start of the study;
Notify the study director/scientists and the analysts of any issues noted during the data review;
Be available to answer scientists and analysts questions regarding reviewed points;
Ensure accuracy of the calibration/verification of all equipment used;
Ensure SOP/SP requirements are followed;
Answer Quality Assurance reports promptly and in a clear and concise manner, when required;
Ensure all tasks are performed in accordance with GLP, where applicable;
Provides regular feedback on analyst performance to their immediate supervisor;
Write and revise SOPs, when required;
Work performed in an office/laboratory environment;
Work within tight and changing deadlines sometimes.
B.Sc. degree in biologie, biochemistry or related field with a minimum of 3 to 5 years of experience, or comparable work experience;
Knowledge and experience in an analytical laboratory environment using HPLC-UV and/or LC-MS/MS;
A minimum of 3 years of relevant experience in a laboratory GLP environment;
Strong knowledge of related legislation, principles, practices and procedures;
Strong knowledge and application of GLP;
Knowledge of Office Word and Excel, knowledge of GraphPad and other HPLC-UV and/or LC-MS/MS software, is an asset;
Bilingualism (French & English) is mandatory;
We can't wait to meet you! Send us your CV today!
- Extended health care
- Mutuelle optique
- Vacation & paid time off
- Assurance vie
- Parking d'entreprise
- Programme de santé
- Événements d'entreprise
- Employee assistance programs
- Horaires de travail flexibles
- Dental care
- RRSP Match
- Tenue décontractée
- Disability insurance
- Commuter benefits
Type d'emploi : Temps Plein
- GLP environment: 2 ans (Souhaité)