Lead vehicle program management from concept to start of production, coordinating cross-functional teams, schedules, budgets, and quality to ensure on-time, on-cost launches.
Responsibilities
Build and own integrated master schedule
Confirm gate deliverables and track critical path
Manage scope and engineering changes
Run weekly cross-functional program meetings
Facilitate gate reviews and provide CEO recommendations
Requirements
Bachelor’s or Master’s degree in Engineering (Mechanical, Manufacturing, Industrial, or related field)
The Catastrophe Modeling Analyst is responsible for collecting, organizing, reviewing, cleansing, interpreting, analyzing, documenting, and distributing catastrophe modeling exposure data and results.
Responsibilities
Processing insured exposure schedules for per-account catastrophe modeling and ensuring data integrity
Perform review and profiling of property and casualty exposure data to assess completeness, consistency, and overall data quality
Validate exposure data against premium bordereaux, claims reported, and facultative placements to identify discrepancies, gaps, or data issues requiring resolution
Format and prepare exposure data for internal and external use, including outputs to reinsurers and outputs to catastrophe modeling platforms such as AIR
Interpret data, analyze catastrophe model results, and provide ongoing reporting to support underwriting, actuarial, reinsurance, and business decision-making
Requirements
BS in Geo Science
BS in Meteorological Engineering
Nice to have: Catastrophe modeling exposure experience
Product and process expert responsible for the entire commercial lifecycle of biopharmaceutical products, ensuring robust manufacturing processes, regulatory compliance, and continuous improvement.
Compensation
Salary Range:
27.510,00 € - 51.090,00 €
Responsibilities
Own product and process knowledge throughout the commercial biologics product lifecycle
Monitor process performance through data trending and statistical analysis
Maintain oversight of drug substance manufacturing processes and provide expert process support
Create, review, and maintain technical, validation, and lifecycle management documentation
Lead and support investigations, root-cause analyses, and implementation of corrective and preventive actions
Requirements
University degree in Biotechnology, Pharmacy, Chemistry, Chemical Engineering, Pharmaceutical Technology, or another relevant scientific field
Nice to have: Leading projects in a cross-functional environment
Nice to have: Using statistical tools and performing data analysis
Intern to support clients in workforce and organization transformation initiatives, including organizational design, change management, and data-driven insights.
Compensation
6-month internship and €8 meal vouchers per working day
Responsibilities
Drive organizational design initiatives
Collaborate with clients and conduct assessments
Analyze data and develop insights
Contribute to project delivery
Implement tailored solutions
Requirements
Master’s degree in Economics, Organization, Management Engineering or similar
Lead NDT Level III professional responsible for leadership, training, certification, process improvement, and customer engagement at the Hampton facility.
Compensation
Anticipated Pay Range: $90K-110K per year.
Responsibilities
Establish and execute training and certification program for all NDT personnel
Maintain certification records in accordance with industry and business requirements
Serve as NDT expert inspector, trainer, auditor, and customer advocate
Validate effectiveness of NDT methods through audits and production iteration
Lead contract review efforts on NDT related customer and industry requirements
Requirements
Bachelor’s degree in engineering or related NDT discipline
Associate degree in NDT with 2+ years of relevant work experience
4+ years of relevant work experience as a certified Level 2
Nice to have: Current Level 3 Certification
Nice to have: Previous NDT experience in investment castings
Lead the design, development, and optimization of diagnostic assay reagent kits and consumables for LC-MS/MS in vitro diagnostic products.
Responsibilities
Provide scientific and technical leadership for the design and development of LC-MS/MS diagnostic assays, reagent kits and associated consumables from feasibility through product launch.
Lead the technical execution of complex assay development projects, translating customer, product and regulatory requirements into robust assay designs, performance requirements and analytical specifications.
Develop and optimize assay methodologies, reagent formulations and experimental strategies to ensure products meet defined performance, quality, robustness and manufacturability requirements.
Define appropriate analytical performance, verification and validation strategies, ensuring that studies are scientifically sound, appropriately risk-based and compliant with applicable regulatory requirements and technical guidelines.
Lead technical feasibility activities, including assessment of assay concepts, prototypes, materials, analytical performance and stability requirements.
Requirements
A degree in a relevant scientific subject with a strong chemistry component or related field is required. An advanced degree (PhD, MSc) is desirable.
Vehicle Program ManagerNewTaiga Motors · Montréal, Canada
Catastrophe Modeling AnalystNewArch Insurance Group Inc. · Manila, Philippines
HR Consultant Workforce & Organization Transformation StageNewMercer · Milan, Italy
Sr. Quality Engineer - HSCNewHowmet Aerospace · Hampton, US