Scientist, ADA, Immunogenicity
Job Summary
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 youre a recent college graduate or seeking your next career opportunity its time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Scientist ADA Immunogenicity 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 Youll 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 Youll 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 be able to easily read and understand study plans and protocols ability to coach/mentor people.
Good communication both written and verbal in French & English.
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 ADA Immunogenicity in particular but without limitation for the following reason(s):
The requirement to have study protocols read and documented in English as required by industry regulatory agencies
What We Offer
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences Benefits Package Includes:
Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & Telehealth Programs
Telework when applicable
Altasciences Incentive Programs Include:
Training & Development Programs
Employee Referral Bonus Program
Annual Performance Reviews
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MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
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!
Required Experience:
IC
About Company
Contract research organization specialized in seamless, end-to-end, early phase drug development, we act to get your most promising compounds into and through early phase clinical trials.