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Systems Analyst

Somerset,NJ

901 Systems Analyst jobs in Somerset,NJ

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Information Systems Technician

U.S. Navy

Dunellen, NJ 08812

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Quality Control Analyst I

Johnson and Johnson

Titusville, NJ 08560

~ 45 min OnsitePaid Time OffRetirement Benefit

  • A minimum one (1) year of experience in a GMP-regulated, science-related field.
  • Basic knowledge of analytical technologies used in the QC laboratory.
  • Skilled in performing basic and some intermediate testing within the functional laboratory, using HPLC and/or UPLC.
  • Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to QC laboratory.
  • Basic knowledge of compendial (USP, EP, JP, etc.) requirements.
  • Basic technical writing skills.
  • Ability to manage an individual project with mentorship from supervision/management.
  • Ability to read and interpret documents such as SOPs, work instructions, test methods and protocols.
  • Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint).
  • Ability to make GMP laboratory decisions both independently and with occasional mentorship from QC Supervisor.
  • Performs independent troubleshooting and has basic root cause analysis skills. Works directly with supervision for resolution of complex issues.
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Software Engineer II, Athena Engine Front End

Amazon Development Center U.S.

New York, NY 10261

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25B Information Technology Specialist

U.S. Army

Bethlehem, PA 18017

~ 1 hr 9 min OnsiteUrgently HiringEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

  • 10 weeks of Basic Training
  • 20 weeks of Advanced Individual Training
  • U.S. Citizen
  • 17 to 34 Years Old
  • High School Diploma or GED
  • Meet Tattoo Guidelines
  • No Major Law Violations
  • No Medical Concerns
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Junior Sales Operations Analyst

Maisons Marques & Domaines

New York, NY 10025

~ 1 hr 1 min OnsiteHealth InsurancePaid Time OffRetirement Benefit

  • Requires a minimum of 1 year of work or internship experience
  • Education: Business, science or engineering B.A. / B.S. degree
  • Should be able to lift up to 30lbs
  • The position is based in New York and reports to the office Monday-Friday
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New, Posted 16 hours ago
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Senior Software Engineer (Hybrid)

Energy Solutions

New York, NY 10279

$140,000-$175,000/yr
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Quality Assurance Specialist

the fedcap group

New York, NY 10017

$66,300-$75,000/yr
~ 1 hr 1 min OnsiteBilingual Preferred

  • A bachelor's degree in a related discipline required.
  • 3-5 years' experience in Quality Assurance, monitoring, and/or Compliance experience in a similar role.
  • Experience with Continuous Quality Improvement frameworks and instruments.
  • Experience in accurate electronic data analysis and QA.
  • Prior experience responding to external audit reports and preparing corrective action plans.
  • Experience in developing and implementing processes for continual quality improvement.
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Controls Service Technician

Johnson Controls

Edison, NJ 08818

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Materials Manager

Illinois Tool Works

Cranbury, NJ 08512

$95,000-$115,000/yr
~ 41 min OnsiteHealth InsurancePaid Time OffRetirement Benefit

  • Bachelor's degree with 3+ years in purchasing/sourcing experience and 3+ years in operation or supply chain or equivalent combination of education and experience.
  • 3-5 years of work experience in manufacturing environment preferred.
  • Strong proficiency in ERP systems (Infor Preferred).
  • Demonstrated expertise in sourcing, supplier management, and inventory control.
  • Advanced data analysis skills; able to translate insights into actionable strategies.
  • Proven ability to lead cross-functional initiatives and drive collaboration
  • Strong communication, presentation, and interpersonal skills across all levels.
  • Familiarity with 80/20 principles and lean manufacturing concepts a plus.
  • Understanding of basic business financials and cost drivers.
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Senior Manager, Clinical Programming

Genmab

Plainsboro, NJ 08536

~ 30 min OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

  • Bachelor's degree in Statistics, Computer Science, Life Sciences
  • Master's degree in Statistics, Computer Science, Life Sciences preferred
  • At least 6-8 years relevant experience in a pharmaceutical, biotech, CRO or Regulatory Agency
  • Proficient in SAS programming, 6-8 years experience
  • Demonstrated knowledge of clinical research, metadata management, industry standards (CDISC), FDA & ICH, GCP, and related regulatory requirements
  • Demonstrated experience managing multiple tasks, complex projects and working with cross functional teams delivering to project and portfolio timelines and metrics
  • Strong verbal and written communication skills; independent and effective working in a multi-study, multi-disciplinary atmosphere in a matrix environment
  • Experience in clinical data management and/or trial management experience with technical expertise in standards management and implementation is preferred.
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