Lead flow cytometry, Elisa, Luminex, CTCs and tissue based IHC/mIF projects through assay design, validation. Require to develop and execution assay in a timely manner. Perform assays according to SOPs and support development of new procedures and improvement of existing SOPs. Supervise assigned laboratory staff to ensure efficient organization, quality, development and execution of project(s).
Essential functions of the job include but not limited to:
Strong expertise with flow cytometry, cellular based applications, ex. Elisa, CTCs etc.
Experience with platform: Canto II, Microplate reader, Luminex, ACD ISH, Flowjo software is a must,
Experience in CTC, oncology, immunology or related fields with cellular analysis is a plus.
Experience with tissue based immunofluorescent and immunohistochemistry (IHC) applications
Experience Perkin Elmer Vectra technologies image microscopy analysis, Halo analysis software is a plus
Outstanding skills with project planning, experimental design, oversight and advanced troubleshooting related to execution of projects, documenting and analyzing data and generating detailed reports is required
A team player with good communication skills, ability to work under pressure and multitask
Design and perform experiments, independently and accurately analyze and present data
High quality output is essential with the ability to build efficiency into improving productivity metrics
Work with the manager, VP to develop project timelines and track to these timelines
Train and mentor junior staff in techniques, data analysis and presentation
Assist in establishing and improving all procedures and required SOP documentation
Responsible for trouble shooting and correcting scientific issues/problems
Identify, update and implement emerging laboratory techniques
Responsible for ensuring all equipment in the laboratory is appropriately qualified, that preventative maintenances are performed as scheduled by the Facilities team and that team members are thoroughly trained in the correct use and maintenance of the equipment
Maintain and support safe lab practices and environment
Work collaboratively with other technical teams in resource sharing and providing technical expertise
Monitor Product and Service/R&D related project expenses
Act as a scientific resource externally to clients and internally
Assists with writing, reviewing and editing contract and grant applications/proposals as appropriate
Assist with writing and publishing papers, abstracts, techniques/or chapters to maintain the scientific standard and image of the company.
May present completed work at appropriate scientific meetings and in publications
Supervision of project assigned laboratory staff to ensure efficient organization, quality, development and execution of project(s)
Other duties as assigned
D. Cellular/Cancer Biology, Immunology, Stem Cell, Fetal Cell Biology or related fields
and 3 years’ relevant laboratory experience; or
Master’s Degree and 5+ years’ relevant laboratory experience
Ability to prioritize tasks and supervise technical staff
Excellent communication, interpersonal, and organizational skills required
Must have the ability to organize and analyze data, as well as, prepare reports
Must possess strong computational skills, preferably experienced with Word, Excel, Power Point, GraphPad and Prism
Excellent use of judgment and discretion required
Extended work hours may be occasionally necessary in order to meet business demands
Ability to lift and carry between 1-15 lbs.; frequently required to sit, grasp, and use right/left finger dexterity; May be exposed to a cold freezer environment (Freezer temperatures range between -20ºC -196ºC)
Must be able to read, write, speak fluently and comprehend the English language
Knowledgeable on molecular assay development for platform of PCR, ddPCR, Nano string, Illumina, NGS etc.
A solid understanding of current GLP and/or ISO/CAP/CLIA standards
Demonstrated skills in biomarker assay development in Oncology field
Experience supervising technical personnel
Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.