1172 Associate Tech Support Analyst jobs in New Jersey

Bachelor's degree in biomedical science with an interest/experience in histology and immunohistochemistry assay development.
Minimum of 5 years Research experience
Multiplex immunohistochemistry staining on Leica Bond and Roche Discovery/Benchmark Ultra Plus platforms are a plus.
Eligibility for American Society for Clinical Pathology (ASCP) certification for Histotechnician (HT) or Histotechnologist (HTL) desired but not required.
Experience managing human tissues and working with Laboratory Information Management Systems (LIMS).
Understanding and experience with CAP Accreditation requirements is a plus.
Excellent written and verbal communication skills and experience with Excel and PowerPoint.
Positive and open mindset and willingness to work in multidisciplinary teams in close collaboration with pathologists and other scientists.
Knowledge of pre-clinical tissue processing and biomarker development is desired but not required.

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Associate Manager, Software Engineer

L3Harris Technologies

Camden, NJ 08103

OnsiteBilingual PreferredEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's Degree with a minimum 6 years prior relevant experience. Graduate Degree with a minimum of 4 years of prior related experience. In lieu of a degree, minimum of 10 years of prior related experience.
Experience in a senior engineering, technical lead, or informal leadership role
Demonstrated experience designing, developing, or integrating RESTful services in a production environment.
Ability to obtain DoD Secret security clearance
Strong communication skills and the ability to collaborate across disciplines and programs.
Exposure to proposal development, cost estimation, or EVMS-driven program environments.
Experience working in an Agile or hybrid Agile development environment.

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PLS Associate Scientist I

Pace Analytical Life Sciences

Lebanon, NJ 08833

$25/hr

OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Associate's degree required, Bachelor's degree in STEM preferred, or a closely related field; OR an equivalent combination of education, training, and experience
Understanding of standard testing tools, instruments, and calibration
Computer applications and systems related to the work
Principles and practices to serving as an effective project team member
Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations
Correct business English, including spelling, grammar, and punctuation
Performing fundamental professional-level CQ duties in a variety of assigned areas
Overseeing and administering standard CQ functions
Serving as a team member and the development and management of projects
Operating in a both a team and individual contributor environment
Preparing fundamental functionals reports, correspondence, and other written materials
Using initiative and independent judgment within established department guidelines
Using tact, discretion, and prudence in working with those contacted in the course of the work
Contributing effectively to the accomplishment of team or work unit goals, objectives and activities
Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work
Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time
Exerting up to 50 pounds of force occasionally and/or up to 40 pounds of force frequently to lift, carry, push, pull or move objects
Vision to read printed materials and computer screens
Hearing and speech to communicate in person or over the telephone

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Quality Control Scientist Microbiology

Adecco

Princeton, NJ 08540

$40-$45/hr

OnsiteHealth InsurancePaid Time OffRetirement Benefit

Bachelor's or Master's degree in Microbiology, Biochemistry, Analytical Chemistry, Molecular Biology, or related field
4–7 years of experience in microbiology and/or bio-analytical testing within pharmaceutical, biotech, or regulated industry environments
Or 10+ years of relevant experience in lieu of degree
Strong knowledge of microbiological techniques including aseptic processing, sterility testing, endotoxin testing, ELISA, ddPCR, flow cytometry, viability assays, and cell culture
Experience with method development, validation, and GMP-compliant testing environments
Familiarity with FDA, EMA, and cGMP regulatory requirements
Strong analytical, troubleshooting, and problem-solving skills
Excellent attention to detail and documentation accuracy
Strong communication skills and ability to work both independently and in cross-functional teams
Proficiency in data analysis, laboratory systems, and quality management systems

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