Thermo Fisher Scientific

Engineer

• Design and optimize clinical prompt templates
• Conduct structured prompt experiments
• Translate experimental findings into production-ready prompt configurations
• Operationalize prompt updates using Git and Azure DevOps
• Develop and maintain Python/Linux research scripts
• Define monitoring strategies and evaluation criteria

Dutch Healthcare Prompt Engineer

Data Entry

• Verify data to improve the performance of the AI model.
• Review the output of the model to maintain a quality standard.
• Include feedback to improve the performance.

Data Annotator – English-Australian

Data Annotator

Brazilian Portuguese Data Annotator

Data Annotator – English

Business Development Rep

• Accelerate adoption of CGT instruments and solutions by developing strategic customer relationships
• Build and execute territory strategies to drive bookings and platform adoption
• Identify and engage high-growth accounts
• Maintain pipeline hygiene and forecasting accuracy
• Lead cross-functional deal teams to complete complex opportunities

Business Development Manager

Manager

• Guide innovative IT solutions at Thermo Fisher Scientific as a Senior IT Manager, overseeing key technology initiatives that enable our mission of making the world healthier, cleaner and safer
• Work within the ETO (Engineering, Technology, and Operations) organization, collaborating closely with GBS (Global Business Services) and all other local IT teams
• Engage with key business stakeholders in the P2P (Procure-to-Pay) space and Shared Service Centres
• Collaborate with business leaders to develop and implement strategic technology roadmaps while managing teams across multiple locations
• Support digital transformation through implementation of advanced solutions in areas like cloud computing, data analytics, artificial intelligence, and enterprise systems
• Ensure operational excellence, security compliance, and continuous improvement of IT services while nurturing a collaborative culture focused on customer success

Senior Manager, IT

Software Engineer

• Define and lead the global PCBA Value Engineering strategy aligned with enterprise productivity, modernization, and lifecycle objectives
• Establish governance models, operating cadence, KPIs, and reporting mechanisms to ensure transparency, accountability, and measurable results
• Develop and maintain a multi-year PCBA modernization roadmap tied to cost savings, risk mitigation, platform consolidation, and supply chain resilience
• Serve as executive-level technical authority for PCBA value engineering initiatives across divisions
• Build and manage a robust pipeline of Value Engineering (VAVE) initiatives to achieve annual and long-range productivity targets
• Lead business case development including NPV, ROI, capital requirements, risk analysis, and resource planning
• Partner with Finance and Procurement to align savings recognition and investment prioritization
• Drive accelerated implementation of modernization and redesign programs to support NPIs and lifecycle management
• Lead and develop a high-performing global team of electrical engineers focused on alternate component selection, redesign, validation, and supplier implementation
• Oversee complex PCBA redesign programs requiring cross-site validation, regulatory consideration, and supplier coordination
• Ensure technical rigor in component lifecycle management, obsolescence mitigation, and risk reduction strategies
• Partner with R&D, Manufacturing, Quality, Operations, and Procurement leaders to align technical solutions with business priorities
• Support EMS Category Management through technical RFQ evaluation, VAVE ideation, and supplier capability assessments
• Drive strategic collaboration with Tier 1 and Tier 2 EMS partners to enhance manufacturing efficiency, test optimization, and cost structure
• Identify enterprise-wide best practices and institutionalize standard work across divisions
• Enable platform consolidation, design harmonization, and test efficiency improvements
• Facilitate engineering changes through PLM systems while ensuring compliance with regulatory and quality standards

Director, PCBA Value Engineering

Program Manager

• Lead end-to-end program execution across Microsoft Security (Purview) initiatives.
• Align Centific’s AI data fundary with Microsoft’s data governance, compliance, and security product strategy.
• Translate joint discussions into structured execution plans, pilots, and scalable deployment models.
• Ensure technical and operational readiness for co-sell and customer rollout scenarios.
• Drive cross-functional execution across Microsoft Healthcare research, engineering and go-to-market teams.
• Partner with Microsoft product teams to align AI data services with healthcare AI priorities.
• Serve as the integration lead between Sales, Product, Engineering, and Microsoft GTM teams.
• Develop scalable alliance playbooks for Security and Healthcare verticals.

Director, Program Management

Product Manager

• Develop and communicate a clear, compelling product vision and roadmap aligned with organizational goals
• Conduct detailed industry research, competitor analysis, and customer/end user discovery to uncover opportunities and translate them into actionable product initiatives
• Proactively monitor industry trends, regulatory changes, and advancements in clinical research technology, especially related to AI-driven data solutions
• Translate complex business requirements into detailed product specifications, features, and user stories that lead to exceptional software experiences and business outcomes
• Drive agile product development, ensuring clarity in requirements, rapid iteration, and continuous delivery of high-quality, impactful features
• Champion exceptional user experience, consistently validating solutions through rigorous user research, analytics, and testing
• Closely collaborate with internal stakeholders, clinical experts, data scientists, and external partners to ensure products exceed expectations and deliver measurable value

Director, Digital Product Manager – Clinical Execution

Research Analyst

• Performs and coordinates all aspects of the clinical monitoring and site management process
• Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation
• Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs
• Ensures audit readiness
• Develops collaborative relationships with investigational sites

Clinical Research Associate – Level II or Senior

• Support the global execution of the site Quality Management System (QMS)
• Analyze deviation trends to identify systemic gaps and improvement opportunities
• Lead and facilitate investigations for deviations, nonconformances, and quality events
• Mentor, train, and coach Investigators and Approvers in effective root cause analysis
• Collaborate with cross-functional teams to implement and verify corrective and preventive actions

Senior Deviation Management Engineer

Project Manager

• Lead the framing, identification, prioritization, resourcing, and execution of large-scale programs focused on cost-out, value engineering, quality improvement, supplier sourcing, or delivery initiatives across multiple divisions
• Drive cross-functional teams to achieve project goals, fostering collaboration and continuous improvement
• Build and maintain a project dashboard on key performance indicators, providing regular updates to senior leadership on project status, risks, and expected outcomes
• Champion the adoption of standard methodologies in cost reduction and operational efficiency, sharing knowledge and methodologies across the organization
• Collaborate with the Value Assurance group and its organization partners to establish and refine project selection criteria for annual objective planning
• Lead steering committee meetings to review project progress, address challenges, and ensure strategic alignment

Director, Project Management – Product Cost Innovation

Vice President

• Ensuring the highest possible quality of input into significant requests for proposals (RFPs)
• Development strategy and regulatory issues
• Drug class issues
• Protocol and indication considerations, including safety
• Team education on indication
• Interactions with client’s physicians and/or client area indication leaders prior to and during bid defenses
• Identifying business opportunities for the PPD clinical research business
• Supporting outstanding input into other areas of the PPD clinical research business activities
• Pro-active client engagement: peer-to-peer interactions with therapeutic area leaders and senior directors of companies whose portfolio contains drugs of business interest
• Strategic alliance development & support
• Client governance and advisory boards
• Providing therapeutic and developmental expertise to internal teams, including indication specific training for clinical teams
• Guidance during clinical trial executions
• Investigator Brochure, clinical study report, NDA/MAA clinical packages development, and other regulatory briefing documents authoring and review
• Contribute to design and reporting of feasibility studies
• Liaise with investigators and KOLs
• Mentor and supervise clinical scientists
• Participate in multidisciplinary teams and working groups to contribute to innovative initiatives

VP, Medical Science & Strategy – Cardiovascular

Account Executive

• Own executive-level relationships with state, local, and public health laboratory systems, serving as the strategic lead for long-term partnerships tied to surveillance, preparedness, and lab modernization initiatives.
• Define and execute multi-year account strategies that expand enterprise-wide engagement across statewide, multi-site public health organizations.
• Lead highly complex, high-value government RFPs, RFQs, and RFIs, serving as the single-point commercial owner across technical, financial, regulatory, and operational workstreams.
• Shape and negotiate multi-year, statewide, and cooperative purchasing agreements, ensuring compliance while maximizing strategic and financial outcomes.
• Travel extensively to key public health laboratories, health departments, and government agencies to influence executive decision-making and advance strategic initiatives.
• Act as a trusted advisor to laboratory directors and public health leaders, translating policy, funding, and testing priorities into scalable solutions.
• Lead and influence cross-divisional teams without direct authority, mobilizing sales, marketing, operations, portfolio, legal, and finance to deliver unified public health solutions.
• Provide market intelligence on public health funding, policy, and laboratory trends to shape regional and national strategies.