• Flow Cytometry Development Scientist II

    Actalent (Miami, FL)


    Description

    The Sr Development Scientist will be part of the Flow Cytometry Development team, responsible for evaluating and implementing new technologies related to assay and instrument development.

    Job Duties:

    Lead and participate in planning, strategy, and execution of studies for the development, evaluation, and optimization of assays related to flow cytometry systems, including hardware, software, and reagents.

     

    Perform work within well-defined boundary conditions and timelines, review, analyze, summarize data, and present results to the broader team.

     

    Write and review study plans, procedures, and reports to ensure compliance with standards, policies, and procedures.

     

    Exercise judgment within defined product concepts to identify and troubleshoot technical issues and drive resolutions.

     

    Collaborate with stakeholders to achieve project objectives and deliver timely solutions.

     

    Support daily management of project timelines with the Program Manager and Project Lead to enable accurate projection of completion dates and effective prioritization of tasks.

     

    Skills

     

    Chemistry, Flow Cytometry, Process development, Biochemistry, Elisa, Cell culture, Molecular biology, Gmp, Assay, Biology, Cgmp, Assay development, Quality control, Research & development, New product development, Immunoassay

     

    Top Skills Details

     

    Chemistry,Flow Cytometry

     

    Additional Skills & Qualifications

    Top 3 Must-Have Skills or Qualities:

    -Technical Expertise in Flow Cytometry: A solid technical experience in high complexity, multi-color flow cytometry assays with state-of-the-art understanding.

     

    - Document Design and Statistical Analysis: Strong skills in designing and writing essential development documents, reviewing and interpreting statistical analysis of study data, and summarizing into study reports.

     

    - Product Cycle and Design Control Knowledge: Familiarity with product cycle and design control requirements, including initial development, feasibility activities, characterization, verification and validations, and design transfer. Knowledge in the development of IVD diagnostic products is desired.

    Qualifications & Requirements:

    Educational: Degree in Biological Science, Immunology, Bio-Medical Engineering, or related field with relevant experience (PhD with 2 years, MS with 3 years, or bachelor’s with 5 years).

    Technical Skills:

    - Expertise in high complexity, multi-color flow cytometry assays, and proficiency in designing and writing development documents, statistical analysis, and summarizing study reports.

    Product Development Knowledge:

    -Familiarity with product cycle and design control requirements, and knowledge in IVD diagnostic products development.

    Attention to Detail and Problem-Solving:

    - Meticulous attention to detail, proficient reasoning, and problem-solving skills in experimental design, data analysis, and interpretation.

    Scientific Method and Statistical Tools:

    -Good understanding of the scientific method, various experimental designs, statistical data analysis approaches, and proficiency in tools like JMP or Minitab.

    Organizational Skills:

    - Excellent organization and time management skills to efficiently evaluate, prioritize, and handle multiple tasks and priorities.

    Experience Level

    Expert Level

    Pay and Benefits

    The pay range for this position is $40.00 - $41.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

     

    • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully onsite position in Miami,FL.

     

    Application Deadline

     

    This position is anticipated to close on May 23, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.