Qc Supervisor

Altasciences is a forward-thinking, mid-size contract research organization offering pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies, including formulation, manufacturing and analytical services. For over 25 years, Altasciences has been partnering with sponsors to help support educated, faster, and more complete early drug development decisions. Altasciences’ integrated, full-service solutions include preclinical safety testing, clinical pharmacology and proof of concept, bioanalysis, program management, medical writing, biostatistics, and data management, all customizable to specific sponsor requirements. Altasciences helps sponsors get better drugs to the people who need them, faster.

**Primary Responsibilities**:
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.

**Tasks Performed**:

- 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 bioanalytical data and all other QC associated task for bioanalytical project
- 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 evaluations 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;
- Perform any other duties as required

**Desired Profile**:

- DEC or Bachelor degree 5 year of experience in QC review of projects.
- Must understand the general SOPs and knowledge in GLP regulations.
- Excellent knowledge of QC review and ability to work in environment with high level of priority and resource adjustments.
- Knowledge of execution of bioanalysis project in CRO environment and experience with staffing logistics are an asset.
- Excellent organizational skills,
- Attentive to details, excellent interpersonal skills, highly flexible, sense of urgency, good sense of responsibility/accountability,
- Client oriented, good communication (both written and verbal in French & English).

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Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences