Logo of Huzzle

Associate Scientist, Flow Cytometry

image

Altasciences

Sep 14, 2024

  • Job
    Full-time
    Mid Level
  • Research & Development
  • Laval
  • Quick Apply

AI generated summary

  • You need a degree in a relevant field, 3 years of experience in regulated studies, knowledge of GLP, strong organizational and troubleshooting skills, and bilingual communication in French and English.
  • You will review data, assist in report writing, manage timelines, order materials, conduct lab work, update SOPs, communicate progress, and ensure compliance with regulations and safety standards.

Requirements

  • - Ideally College degree and/or University degree in Chemistry, Biochemistry, Immunology or applicable field.
  • - Preferred experience in regulated clinical and/or preclinical studies.
  • - 3 year of experience.
  • - Knowledge of regulatory agency guidelines and must understand general SOPs and have good knowledge of GLP regulations.
  • - Good organizational skill.
  • - Excellent troubleshooting skills.
  • - Able to easily read and understand study plans and protocols.
  • - Attentive to details.
  • - Ability to coach/mentor people.
  • - Client oriented.
  • - Highly flexible.
  • - Sense of urgency.
  • - Good communication both written and verbal in French & English.

Responsibilities

  • - 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.

FAQs

What is the role of the Associate Scientist, Flow Cytometry at Altasciences?

The Associate Scientist supports the senior scientist by assisting with various tasks based on scientific competency and training, which may include laboratory bench work, data analysis, and writing reports.

What qualifications are ideal for this position?

Ideally, candidates should have a college or university degree in Chemistry, Biochemistry, Immunology, or an applicable field, along with a preferred experience in regulated clinical and/or preclinical studies.

How many years of experience are required for this position?

A minimum of 3 years of experience is required.

What are the key skills needed to succeed in this role?

Key skills include good organizational and troubleshooting skills, attention to detail, the ability to understand study plans and protocols, client orientation, flexibility, a sense of urgency, and proficiency in both written and verbal communication in French and English.

Are there opportunities for training and development in this position?

Yes, Altasciences offers training and development programs as part of their incentive programs.

What types of benefits does Altasciences offer?

Benefits include health/dental/vision insurance plans, 401(k)/RRSP with employer match, paid vacation and holidays, paid sick and bereavement leave, employee assistance and telehealth programs, and telework when applicable.

What is the work environment like at Altasciences?

The work environment is described as passionate and collaborative, where all employees play an important role in the discovery and development of new drug therapies.

Are there any specific compliance regulations that need to be followed?

Yes, all work must be conducted in compliance with applicable SOPs, GCPs, GLPs, and company guidelines and policies.

Does this position involve mentoring or coaching?

Yes, the Associate Scientist should have the ability to coach or mentor other staff members.

How does Altasciences approach diversity and inclusion in the workplace?

Altasciences is committed to diversity and inclusion, aiming to attract, develop, and retain talented employees from diverse backgrounds to benefit from varied experiences and perspectives.

Quicker go/no-go decisions with integrated preclinical, clinical, bioanalytical, manufacturing, and CRO services.

Science & Healthcare
Industry
1001-5000
Employees
1992
Founded Year

Mission & Purpose

Outsourcing made easy with a one-stop solution to early phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 25 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!

Culture & Values

  • Respect

    We are open to differences of opinions and value different viewpoints. We treat each other, our customers, participants in our studies, and the research animals in our care with dignity.

  • Quality and Excellence

    We provide services and solutions of the highest quality, and pride ourselves on challenging the status quo. We strive to exceed expectations by truly giving our best at everything we do.

  • Integrity

    We are honest and uphold strong moral principles. We conduct our business with transparency and high ethical standards.

  • Customer Focus

    We actively partner with our clients. We listen, remain accessible, deliver on commitments, and maintain open channels of communication to build and nurture a lasting relationship based on trust.

  • Employee Development

    We provide leadership, encourage professional development, recognize individual and team contributions, and offer a stimulating, safe working environment.