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Python Developer

Durham,NC

1374 Python Developer jobs in Durham,NC

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Business Development Rep - Training Provided

Globe Life Liberty National Division: Wagner Agencies

Raleigh, NC 27610

$80,000-$150,000/yr
~ 31 min Onsite

  • High school diploma or GED
  • Driver License
  • Willing to undergo a background check
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Senior Psychometrician

MetaMetrics

Durham, NC 27713

New, Posted 10 hours ago
Territory Sales Representative

Southeast Elevator

Raleigh, NC 27607

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Director - Energy and Physical Plant

Wake County Public School System

Raleigh, NC 27610

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Quality Management Systems (QMS) Manager

Pentair

Apex, NC 27502

$95,500-$177,300/yr
~ 27 min OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

  • Bachelor's degree in engineering, Quality Management, Manufacturing, Business, or a related technical discipline
  • 7+ years of progressive quality experience in a manufacturing environment
  • 3+ years managing or administering Quality Management Systems
  • Experience leading ISO 9001 implementation, certification, or maintenance activities
  • Demonstrated success in developing procedures, audit programs, and quality governance systems
  • Experience with corrective action systems, root cause analysis, and continuous improvement methodologies
  • Proven ability to influence cross-functional teams and drive organizational change
  • Strong knowledge of ISO 9001 and quality system requirements
  • Proficiency in internal auditing principles and practices
  • Knowledge of CAPA, document control, risk management, FMEA, SPC, APQP, and process management
  • Experience with quality management software and document management systems
  • Advanced analytical skills using Excel, Power BI, or similar reporting tools
  • Travel: Approximately 25% travel to include domestic and international destinations to visit Pentair facilities and various supplier locations. Travel as required by car, air, etc.
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FSP Associate Manager, Safety Data and Systems - Pharmacovigilance

Thermo Fisher Scientific

Durham, NC

Onsite

  • At least Bachelors' degree (or country equivalent) in computer science, data science, computational linguistics, applied statistics/biostatistics, life sciences / Information technology or other relevant field required.
  • Python, ML/NLP frameworks, model deployment/monitoring, MLOps tooling, ideally exposure to LLMs on unstructured clinical/safety text.
  • Working understanding of safety database data models (Argus/ArisG) and E2B(R3) structure.
  • Relevant experience in IT / Safety / Clinical Research / Pharmacovigilance overall with at least 3 years of proven experience with safety database systems (e.g. ARGUS or ArisG) including workflow management
  • Equivalent and adequate combination of education and experience or proven practical expertise in all of the required skills
  • Proficiency in Python for ML development, including scikit-learn, pandas, NumPy; experience with at least one deep learning framework (PyTorch or TensorFlow).
  • Natural language processing for extraction of adverse events, drugs, and outcomes from unstructured text - case narratives, medical literature, call transcripts, and spontaneous reports.
  • Named Entity Recognition (NER), relation extraction, and text classification
  • Experience with transformer-based / large language models (BERT-family, clinical/biomedical models such as BioBERT or PubMedBERT, and modern LLMs) for narrative generation, summarization, and information extraction.
  • MedDRA and WHODrug auto-coding using ML/NLP; prompt engineering and retrieval-augmented generation (RAG) a plus.
  • Supervised and unsupervised methods for classification, clustering, and anomaly detection.
  • Feature engineering and model evaluation (precision/recall trade-offs, ROC/AUC, calibration) with an understanding of why recall and sensitivity are weighted heavily in a safety context.
  • Model lifecycle management: versioning, monitoring, drift detection, retraining pipelines using standard MLOps tooling (e.g. MLflow, Azure ML, Databricks) in line with client DT/BIS standards
  • Model explainability / interpretability (SHAP, LIME) - essential where decisions must be defensible to health authorities.
  • Understanding of GxP / GAMP 5 validation as applied to AI/ML systems, model governance, and emerging regulatory expectations (EMA reflection paper on AI, FDA guidance) — rare and worth flagging as preferred.
  • Proficiency in Safety Database systems (e.g. Argus) and knowledge of other technical systems applicable to Safety /Pharmacovigilance (e.g. E2B gateway, safety signal detection tools and systems) is a plus.
  • Proficiency in electronic systems commonly used for Safety / PV, like for data visualization and analysis, dashboards
  • Solid understanding of the quality management processes, metrics and KPIs
  • Good knowledge of relevant pharmacovigilance regulatory requirements and guidance documents (including Europe, US, Japan)
  • Proficient in the Microsoft 365 stack (Excel, Word, PowerPoint, Teams, SharePoint, OneDrive) and in modern collaboration and documentation tooling
  • Advanced Excel required; working proficiency in SQL required for querying safety and operational datasets
  • Fluent communication in written and spoken English required
  • Ability to work independently with minimal oversight and prioritize effectively
  • Ability to complete multiple complex deliverables within tight timelines
  • Ability to function effectively in a team environment
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Manufacturing Engineer

AAR

Durham, NC

Onsite

  • Manufacturing or Mechanical Engineering Degree (BS) from a four-year college or university and a minimum of five years related experience; or equivalent combination of education and experience.
  • Experience with mechanical systems and lean manufacturing principles.
  • Familiarity with a diverse range of materials (i.e. aluminum alloys, stainless steel alloys, engineering polymers, composites, etc.).
  • Must have the ability to read and interpret engineering drawings, specifications and technical data.
  • Must be capable of applying statistical analysis techniques such as Design of Experiments, Optimization, Process Reliability, Hypothesis Testing and Regression Analysis.
  • Experience with 3-D Modeling software (Uni-graphics, Solid Works, or Solid Edge) is required.
  • Must have strong analytical and mechanical troubleshooting skills.
  • Read, write, speak and understand the English language.
  • Experience within commercial aircraft seating (assembly) environment.
  • Lean implementation with emphasis on standard work & line balancing.
  • Experience establishing operational objectives and performance metrics.
  • DMAIC problem solving
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New, Posted 22 hours ago
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Mechanical Engineer Specialist - Structural Analysis (Nuclear)

Flowserve

Raleigh, NC 27602

~ 31 min Onsite

  • Master's degree in Mechanical Engineering or equal.
  • 8-10 years in applied structural mechanical analysis, specifically rotating equipment.
  • Nuclear Industry experience.
  • Background working within a customer-oriented working environment.
  • Extended knowledge of Microsoft Office programs, Finite element analysis packages (ANSYS/ABAQUS), and 3D modeling software (SolidWorks).
  • Skilled at performing hand calculations and/or rough order of magnitude calculations
  • U.S. citizen or Green Card Holder required
  • Fluent in the English language.
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Youth Development Specialist - Relocation to Hershey, PA Required

Milton Hershey School

Durham, NC 27703

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Clinical Outcome Assessments Manager

Manpower Group

Durham, NC 27701

$65-$80/hr
RemoteFlexible ScheduleHealth InsuranceRetirement Benefit

  • A current, up-to-date resume
  • Bachelor's degree in Psychometrics, Health Outcomes Research, Epidemiology, Biostatistics, Public Health, Behavioral Science, Biomedical Engineering, Data Science, or a related field
  • 3+ years of relevant experience in pharmaceutical, biotechnology, digital health, CRO, or academic environments
  • Demonstrated expertise in Clinical Outcome Assessments (COAs), patient-centered outcomes, or measurement science disciplines
  • Experience with qualitative research methodologies, psychometrics, and statistical analysis techniques
  • Strong understanding of regulatory standards related to patient-focused evidence and outcome assessments
  • Ability to take an extended work break from mid-December through early January, as required for the assignment
  • Ability to meet compliance requirements
  • Must be eligible and provide proof of eligibility to work in the US
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