Associate Scientist (BSD)

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. About The Role The Associate Scientist is the right-hand help for the senior scientist. As such their responsibility is mainly to assist the senior scientist with tasks based on scientific competency and training. Based on competencies the Associate Scientist may be assigned as BPI and will oversee and manage bioanalytical studies under supervision. What You’ll Do Here Tabulate and perform final data batch review by performing multi-batch trend analysis, completing all study documentation as required including approving of Memo to File or SOP/Protocol/Study Plan deviations where appropriate. Provide report and/or final results within study timelines and ensure any deviation, exception or events are reflected as appropriate and assure that all analysis conducted are reported and accurate. Assist in writing validation and analytical plans/reports and provide comments and/or recommendations, as needed, for the bioanalytical portions of preclinical and clinical protocols, study plans, laboratory manuals, Data Transfer Agreements, and/or other document. Assist for planning sample analysis by maintaining timeline and scheduling commitments. If assigned, perform the ordering of reagents, materials and if assigned verification of inventory. Perform literature searches and draft work plans for the development of assays as assigned. Assist with evaluation of risk and costing. Based on training and competency, perform laboratory bench work for method development or validation, interpretation of results, documentation/tabulation of data and troubleshooting when required. Keeps BPI and/or Senior Scientist involved through ongoing communications. Write, review and update method SOP as needed Support responses to QA reports Assigned by management on studies and tasks based on scientific competency and training (can include method development, validation or sample analysis projects). Provide feedback on progress and assist in sponsor teleconferences as required. Conduct all work in compliance with applicable SOPs, GCPs, GLPs and observes all company guidelines and policies. Respecting Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures. Assist the senior scientist with tasks based on scientific competency and training What You’ll Need to Succeed Minimum of College Degree and Ideally B.Sc or applicable field. 3 years of related experience Must understand general SOPs and have an excellent knowledge of GCP/GLP regulations Ability to read and interpret technical documents and industry specific manuals. Ability to write advanced reports and correspondence. Ability to speak effectively in front of sponsor. Bilingual proficiency in French & English. (Depending on location) Well-developed interpersonal skills are required. Ability to develop strong trusting relationships in order to gain support and achieve results. Good organizational skill, capable of managing multiple conflicting priorities. Excellent troubleshooting skills Attentive to details Be able to easily read and understand study plans and protocols Ability to coach/mentor people Relevant industry experience a plus 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 Associate Scientist (BSD) , 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 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 #LI-MB1 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!

The Associate Scientist assists senior scientists with bioanalytical studies, including data review, method development, and validation. They are responsible for maintaining study timelines, documenting results, and ensuring compliance with GCP and GLP regulations.

Candidates must hold at least a college degree, with a B.Sc preferred, and possess 3 years of relevant industry experience. Proficiency in both English and French is required, along with a strong understanding of GCP/GLP regulations and technical documentation.

• Health insurance • Dental insurance • Vision insurance • 401(k) • RRSP • Employer match • Paid vacation • Paid holidays • Paid sick leave • Bereavement leave • Employee assistance program • Telehealth programs • Training and development programs • Employee referral bonus program

• Project managementPreferred

Identified from the job description. Confirm important requirements above.

• Bioanalytical studies
• Data batch review
• Method development
• Method validation
• GCP compliance
• GLP compliance
• Technical documentation
• Troubleshooting
• Sample analysis
• Laboratory maintenance
• Data interpretation
• Project coordination
• Communication
• Mentoring
• Organizational skills
• Attention to detail
• Health And Safety Standards
• Good Laboratory Practice (GLP)
• Method Development
• Assay Development
• Planning
• Multilingualism
• Customer Service
• Medical Guideline
• Clinical Research
• Training And Development
• Employee Assistance Programs
• English Language
• French Language
• Interpersonal Communications
• Legislation
• Performance Review
• Safety Assurance
• Sample Analysis
• Telehealth
• Trend Analysis
• Troubleshooting (Problem Solving)
• Scheduling
• Enthusiasm

• Science & Research
• Healthcare
• Manufacturing
• Associate Scientist
• Unclassified Specialized Occupation

Minimum education

College diploma

Minimum experience

2+ years

Posting language

English

Working hours

40 hours per week