Job List
Pharmaceutical
7+ years of experience in the biotech or pharmaceutical industry or at an Analytical Development CRO. Apply in-depth knowledge of analytical and pharmaceutical
One to Four years of experience and understanding of quality in the pharmaceutical/health care industry. The Quality Specialist works within Master Control to
Reporting to the Manager, APA, you will be responsible to set up, modify, operate, troubleshoot, and repair several different types of packaging machinery.
Coordinate with clients, NuChem management, animal facility manager and lab manager for smooth execution of studies; Comptitif et selon l'exprience.
Conduct clinical or laboratory studies to test, evaluate and screen drugs, pharmaceuticals and nanoparticles used in biomedical applications.
Conduct clinical or laboratory studies to test, evaluate and screen drugs, pharmaceuticals and nanoparticles used in biomedical applications.
Follow compliance rules, and safety standards. Experience as a delivery driver is not required, we will train the right candidates. Use of an android scanner.
Previous industry experience in a pharmaceutical/nutraceutical manufacturer would be considered an asset. Check reports, records and data for completeness and
Minimum of 2 years of clinical data management experience in the pharmaceutical industry or in a CRO. Create and review electronic case report forms (eCRF) per
MSc or BSc in organic chemistry, medicinal chemistry, pharmaceutical chemistry, applied chemistry, or related field. Good communication and learning skills.
The Inside Sales Representative maintains effective customer relations, develops opportunities for growth within an existing customer base, and assures market
Experience: 2 years to less than 3 years. Health care institution, facility or clinic. Maintain, update and manage health information databases.
The QC data reviewer / associate ensure integrity of review and corrections in compliance with GLP, SOP and study plans. Perform QC sample reception process.
Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs.
Establish and maintain strong relationships with key stakeholders in Quebec - Primarily Montreal/Quebec City. Minimum of 12 years professional experience.
