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Freelance Flow Cytometry Analyst Jobs in Michigan

Obtains biological specimens for analysis (blood cultures, viral cultures, toxicological material, flow cytometry, image analysis, etc.) and performs special procedures such as coronary artery ...

The duties will include microbiology, immune cell isolation from tissues, flow cytometry, pathology ... Analysis of proteins by Western blot and immunoprecipitation Why Join Michigan Medicine? Michigan ...

... using multiparameter flow cytometry to isolate and functionally test these cells. This is an ... Analyze, interpret, and present data at lab meetings and scientific conferences; contribute to ...

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Freelance Flow Cytometry Analyst information

What is a freelance flow cytometry analyst?

Freelance Flow Cytometry Analysts are independent professionals who specialize in the use and analysis of flow cytometry, a technique used to detect and measure physical and chemical characteristics of a population of cells or particles. They typically work on a project-by-project basis for research labs, biotech companies, or clinical organizations, offering expertise in experimental design, sample preparation, data acquisition, and interpretation. Their flexibility allows clients to access specialized knowledge without the need for permanent staff, making them valuable for short-term or highly technical projects.

What are the key skills and qualifications needed to thrive as a freelance flow cytometry analyst?

To thrive as a Freelance Flow Cytometry Analyst, you need a solid background in cell biology or immunology, expertise in flow cytometry techniques, and a relevant science degree. Familiarity with flow cytometry instruments (such as BD FACSCanto or Beckman Coulter systems), data analysis software (like FlowJo or FCS Express), and, in some cases, certifications in flow cytometry are typically required. Strong analytical thinking, attention to detail, and effective communication help you interpret complex data and work independently with clients. These skills ensure accurate experimental results, reliable data interpretation, and successful collaborations across diverse research or clinical projects.

What are some common challenges faced by a freelance flow cytometry analyst, and how can they be managed?

Freelance Flow Cytometry Analysts often encounter challenges such as limited access to laboratory resources, managing multiple client expectations, and ensuring data quality across diverse projects. To address these, it’s essential to maintain clear communication with clients regarding project requirements, timelines, and equipment availability. Building relationships with core labs and staying updated on remote data analysis tools can also help freelancers streamline their workflow and deliver high-quality results consistently.

What is the difference between Freelance Flow Cytometry Analyst vs Laboratory Flow Cytometry Technician?

AspectFreelance Flow Cytometry AnalystLaboratory Flow Cytometry Technician
CredentialsTypically requires a bachelor's or master's in biology, immunology, or related fields; certifications are a plusUsually requires a relevant associate or bachelor's degree; certifications are less common
Work EnvironmentIndependent, contract-based work often remote or on-site at client locationsLaboratory setting within research or clinical labs, often full-time
Employer & Industry UsageFreelance analysts work with biotech, pharma, or research institutions on specific projectsEmployed by labs, hospitals, or research centers performing routine testing

In summary, Freelance Flow Cytometry Analysts typically work independently on specialized projects, requiring advanced education and certifications, while Laboratory Flow Cytometry Technicians are employed full-time in lab settings performing routine tasks. Both roles involve flow cytometry but differ in work environment and employment structure.

What are the most commonly searched types of Flow Cytometry Analyst jobs in Michigan?

The most popular types of Flow Cytometry Analyst jobs in Michigan are:

What job categories do people searching Freelance Flow Cytometry Analyst jobs in Michigan look for?

The top searched job categories for Freelance Flow Cytometry Analyst jobs in Michigan are:

What cities in Michigan are hiring for Freelance Flow Cytometry Analyst jobs?

Cities in Michigan with the most Freelance Flow Cytometry Analyst job openings:

Senior Associate Scientist - Flow Cytometry

Charles River Laboratories, Inc.

Mattawan, MI • On-site

$80K/yr

Full-time

Medical, Retirement, PTO

Posted 8 days ago


Charles River Laboratories rating

8.3

Company rating: 8.3 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical


Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

The Immunotox group supports drug development by investigating immune responses using flow cytometry. The group supports immunophenotyping endpoints, isolation of PBMCs and cell-based stimulation assays. Utilizing these platforms/assays, the team is responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical studies. 

Essential Functions

  • Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight
  • Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area
  • Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight
  • Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations
  • Assist in problem solving for technical and/or regulatory issues with oversight
  • Responsible for writing and preparing study plans/protocols/amendments with minimal oversight
  • Participate in Sponsor visits/tours with minimal oversight
  • Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with minimal oversight
  • Perform data analysis using appropriate software with minimal oversight
  • Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas
  • Demonstrate effective communication skills through informal discussions with peers, supervisor, and team; Function as a liaison, maintaining timely and frequent communication between CRL and
  • Sponsor/Client/SD with minimal oversight
  • Ensure scientific integrity of studies with minimal oversight
  • Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight
  • Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data
  • Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
  • Write, review and approve deviations with oversight
  • Develop knowledge of regulatory and GXP requirements, industry standards and company SOPs within one operational area
  • Effectively manage a small portfolio of research projects including method development and validation while ensuring timelines are met in a single operational area with oversight
  • Performs all other related duties as assigned 
Job Requirements

Qualifications

  • Bachelor’s degree (BA/BS) with 5-7 years of relevant working experience. Master’s degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with no experience
  • Ability to communicate verbally and in writing at all levels inside and outside the organization
  • Basic familiarity with Microsoft Office Suite
  • Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
  • Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts
  • Sometimes on short notice
  • Ability to work under specific time constraints
  • Must be authorized to work in the United States without a sponsor visa, now or in the future.

The pay rate for this role is $80k/year.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.


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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947