Scientist, Flow Cytometry

**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. Â 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.

**About The Role**
The Scientist, Flow Cytometry / ELISpot is assigned to projects based on scientific competency and training. The Scientist will ensure the overall integrity/quality of assigned studies. The Scientist can also be designated as the main contact for client interactions laboratory for their assigned projects.

**What You'll Do Here**
- Assigned by management on studies and tasks based on scientific competency and training (can include method development, validation or sample analysis projects).
- For validations and sample analysis the Scientist can be assigned as Bioanalytical Principal Investigator and is the first point of contact for PM and/or clients for laboratory services and will manage and conduct method development, qualification, validation and production studies for clinical and non-clinical studies in compliance with the protocol/study plan, amendments, GCP, GLPs, SOPs and Best Practices;
- Manage project and order appropriate material, as needed
- When applicable, provide QC support on studies assigned to other team members in laboratory based on training and competencies.
- When applicable, perform data batch review, perform multi-batch trend analysis, complete documentation as required by tracking deviations, events and reports of non-compliance and review or approved Memo to File or SOP/Protocol/Study Plan deviations;
- When applicable, provide a report and/or reporting of results, within study timelines and ensure any deviations/exception events are reflected as appropriate and assure that all analysis conducted is reported and is accurate;
- Manage as to maintain timeline and scheduling commitments
- When applicable review and provide comments and recommendations, as needed, for the bioanalytical portions of preclinical and clinical protocols, study plans, laboratory manuals, Data Transfer Agreements, and/or other document, as needed;
- Support and mentor Analysts in the daily operations for completion of sample analysis and/or validation studies and the analysts work;
- Support and mentor other team members based on expertise,
- Responsible for troubleshooting issues within the studies and be able to resolve them independently via development of appropriate procedure.
- Organize and communicate complex data sets in a clear and concise manner to key stakeholders from diverse backgrounds.
- To write, review and updated method SOP as needed
- Participate in meetings with clients, conferences and scientific outreach
- Conduct applicable work in compliance with applicable SOPs, GCPs, GLPs, and observe all company guidelines and policies
- Respecting Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures;

**What You'll Need to Succeed**
- Ideally College degree and/or University degree in Chemistry, Biochemistry, Immunology or applicable field.
- Preferred experience in regulated clinical and/or preclinical studies with typically 3 years of experience.
- Knowledge of regulatory agency guidelines, must understand general SOPs and have excellent knowledge of GLP regulations.
- Good organizational skill.
- Highly flexible, sense of urgency.
- Excellent troubleshooting skills.
- Client oriented.
- Attentive to details.
- Able to easily read and understand study plans and protocols.
- Ability to coach/mentor people.
- Good communication both written and verbal in French & English.
- Must deeply understand general SOPs and have an excellent knowledge of GCP/GLP regulations.

Altasciences strives to provide a French work environment for its employees in Quebec. Altasciences has taken all reasonable measures to avoid imposing the above language requirement. This requirement is essential for the position of **Scientist, Flow Cytometry / ELISpot'‹**, in particular, but without limitation, for the following reason(s):

- The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.

**What We OfferÂ**Â

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

**Altasciences' Benefi