QC Supervisor (LCMS)
at Altasciences
Laval, QC, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Apr, 2025 | Not Specified | 19 Jan, 2025 | 5 year(s) or above | Good communication skills | No | No |
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Employment Type:
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Description:
YOUR NEW COMPANY!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.  No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
Responsibilities:
ABOUT THE ROLE
The QC Supervisor will manage, coach and coordinate Quality Control Review assignments of team. Perform QC review. To assist Management by ensuring proper organization and/or schedule of direct reports on daily basis, provide proper communication of study instructions and work closely with the Scientists and Management to increase the efficiency and ensure appropriate scheduling.
WHAT YOU’LL DO HERE
- Schedule QC work, including in-life QC, on a daily basis, maintain it and ensure that it is efficient
- Support, coach and mentor direct reports in the daily basis for completion of all laboratory studies as scheduled;
- Work closely with Management to ensure the quality control staff work is efficient, ensure to communicate instructions to staff and ensure procedures are followed and are performed in compliance with protocols, SOPs and GLP’s and all applicable regulations
- Perform QC review of Sample Management reception documentations and all other QC associated task for bioanalytical studies
- With the collaboration of the subject matter experts, coach and optimize the usage of the software used in the data generation by the QC reviewer.
- Propose and implement solutions to improve quality, safety and efficiency in the laboratory;
- Ensure that any issues related to quality control of ongoing studies are resolved in a timely manner and communicate to the Management team;
- Coordinate quality control training with assigned trainers and perform technical trainings as needed
- Perform employee evaluation including career path development and provides feedback to Management
- Observe all company guidelines and policies and keep up to date with respect to pertinent regulatory developments in the industry;
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Chemistry biochemistry immunology or applicable field
Proficient
1
Laval, QC, Canada