710 Statistical Programmer jobs in Malvern, PA

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      Director, Statistical Programming

      LARIMAR THERAPEUTICS

      Philadelphia, PA 19102

      Remote

      • Extensive experience of leading both early and late-phase clinical studies including programming and validation of SDTM and ADaM data sets, tables, figures, and listings
      • Experience in managing the Statistical Programming team
      • 10+ years statistical programming experience in biotech/pharmaceutical industry
      • Bachelor's degree or higher in Mathematics, Statistics, Computer Science, or a related field.
      • Expert level SAS programmer with experience in delivering complex programming assignments, macros and analyses
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      CNC Programmer / Operator - 2nd Shift

      Smiths Group

      Swedesboro, NJ 08085

      $27-$30/hr
      ~ 48 min Onsite

      • Make average to complicated mathematical calculations and resolve elementary technical problems
      • Capable of handling multiple priorities
      • Must be detail oriented; be able to work independently using sound judgment
      • Numerical control machining skills experience and ability to read and interpret work related machine drawings
      • Ability to complete tasks in a timely and efficient manner
      • Minimum 3 years of CNC machine tool Programming & Operating experience
      • Good verbal, written, problem solving and organization skills required
      • Can operate a minimum of 2 CNC machine tools
      • High school diploma or equivalent with a technical school education and working machinist knowledge or equivalent
      • Possesses previous experience as a Manual machinist
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      Information Technology Professional (IT Support)

      U.S. Navy

      Malvern, PA 19355

      Education AssistanceHealth InsuranceRetirement Benefit
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      Quality Control Technician 3 2nd SHIFT

      L3 Harris

      Camden, NJ 08105

      ~ 38 min OnsiteBilingual PreferredEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

      • Knowledgeable of Statistical Process Control techniques and statistics
      • U.S. Citizenship required
      • Experience with auditing
      • Team oriented, able to work as part of a program team
      • High School Diploma
      • Proficient in development of manufacturing flow processes and developing inspection plans and inspection procedures, workmanship criteria
      • Knowledgeable in Part Specification; Identification Marking, Packaging
      • Knowledgeable in wiring harness specifications & requirements
      • 2-5 years' experience in Manufacturing Operations of electronic assemblies
      • Knowledgeable in Surface Mount Technology: printing, placement, and soldering processes
      • Able to secure a Security Clearance
      • Experience with Test specifications and equipment
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      Analyst QC CRS

      Johnson and Johnson

      Malvern, PA 19355

      OnsitePaid Time OffRetirement Benefit

      • Familiarity with LIMS, ELN, or comparable laboratory data management systems; solid computer skills and basic data analysis capability.
      • Strong understanding of GMP/GLP principles and experience working in or supporting GMP manufacturing laboratories.
      • Requires the physical ability to lift up to 20 lbs, stand or sit for extended periods of time in a laboratory setting, and ability to perform visual inspections of materials (color, appearance, particles, etc.) and to document observations during laboratory testing
      • Demonstrated experience with flow cytometry, qPCR/ddPCR, and cell-based assays used for release and characterization.
      • Requires ability and flexibility to accommodate unplanned overtime (including nights and weekends) on little to no prior notice outside of Monday-Friday 8:00AM to 4:30PM.
      • Excellent troubleshooting, organizational, and record-keeping skills
      • Minimum 4-6 years of hands-on experience in cell therapy or biologics laboratories; direct CAR-T or T-cell processing experience strongly preferred.
      • Experience with QC documentation practices: SOPs, batch records, test reports, deviation/CAPA processes, and audit readiness.
      • Requires travel up to 5% of domestic travel
      • Strong written and verbal communication skills; ability to interact effectively with cross functional teams and regulators.
      • Excellent attention to detail, organizational skills, and ability to prioritize under time pressure.
      • Minimum of a Bachelor's or equivalent degree in Biology, Biochemistry, Microbiology, Chemistry or related field is required
      • Proficient with Microsoft Office applications (Outlook, One Note, Teams, Excel, Word, and PowerPoint)
      • Working knowledge of microbiological assays relevant to GMP (sterility, mycoplasma, endotoxin) and environmental monitoring practices.
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