Thermo Fisher Scientific

QA Engineer

• Conduct and/or lead client, internal, GCP, directed site, facility, vendor, and subcontractor audits and regulatory inspections
• Provide GCP consultation and support to project teams and external clients
• Participate as a co-auditor in complex system audits
• Perform QA activities including database audits, clinical study report audits, sample results table audits, and process improvement
• Serve as a QA and audit subject-matter resource to operational departments
• Prepare and present audit findings and related information at departmental, internal operations, and client meetings
• Work in office, laboratory, and/or clinical environments
• Handle potential exposure to biological fluids, infectious organisms, and electrical office equipment while using required personal protective equipment
• Work with varied demands, changing conditions, physical activity, and frequent interactions with diverse groups

QA Auditor II

Program Manager

• Provides tactical support for client-facing biopharmaceutical projects
• Manages project performance, with emphasis on program financial management and client communications
• Provides internal consulting on project management issues
• Identifies process and efficiency improvement opportunities
• Identifies and escalates risks affecting project timelines and financial objectives
• Oversees and coordinates study initiation
• Translates protocol language into internal systems and processes
• Prepares for and facilitates internal meetings and attends external meetings
• Coordinates stability launches
• Maintains project setup and sample test scheduling
• Evaluates and manages project timelines and deliverables
• Supports contract management and adheres to contract language
• Manages project setup and financials
• Prepares projections, forecasts, and revenue recognition for fee-for-service, hourly, or FTE programs
• Adjusts forecasts or project priorities weekly as needed
• Communicates routine FTE utilization and spend
• Coordinates internal and external communications
• Assists the client relationship manager with meeting minutes and action items
• Manages study documents and testing directives and shares data/reports
• Supports fee-for-service and hourly contract review processes
• Provides and supports training for Program Manager I
• Participates in cross-functional initiatives and process improvements

Program Manager II – Biopharmaceuticals, GMP

General

• Implement, configure, maintain, troubleshoot, and support Thermo Scientific LIMS products
• Develop and execute computer system validation documentation, including requirements, risk assessments, test protocols/scripts, traceability matrices, validation reports, and associated evidence
• Perform functional, regression, integration, and user-acceptance testing
• Document testing results and investigate test failures and deviations
• Ensure systems and documentation meet applicable GxP/GLP and data-integrity requirements
• Assess system changes, enhancements, upgrades, and defects for validation impact and coordinate appropriate testing
• Maintain controlled validation records, specifications, test scripts, and other lifecycle documentation
• Work with laboratory scientists, QA, IT, developers, project managers, and business stakeholders to translate laboratory requirements into validated solutions
• Lead implementation and validation activities, review other analysts' work, resolve complex issues, provide subject-matter expertise, and support audits/inspections
• Provide technical expertise to LIMS products and computer system validation

Senior Validation Specialist, LIMS

• Execute full Localization QA test cycles across different platforms, OS versions, and testing environments, including Production
• Review, verify, edit, score, and translate copy across a wide range of media and content types
• Validate localized content for tone, grammar, context, cultural relevance, and linguistic correctness
• Evaluate UI behavior for truncation, clipping, alignment, wrapping, and encoding issues
• Report and track bugs clearly and accurately; retest to confirm fixes
• Provide feedback and suggestions regarding linguistic errors, UX issues, and functional defects
• Contribute updates and recommendations to Style Guides and Terminology Databases
• Assist with ad-hoc localization QA tasks, spot checks, and build verifications
• Collaborate with localization PMs, translators, developers, and QA teams
• Suggest process or workflow improvements to increase QA efficiency, scalability, and consistency

Localization QA Tester – Thai

Business Development Rep

• Review, prioritize, and qualify inbound and marketing-generated leads
• Contact prospective customers to understand scientific needs, applications, timelines, and opportunities
• Route qualified opportunities to the appropriate field sales representative
• Support field sales teams with prospecting, account development, and customer follow-up within assigned regions
• Follow up on leads from campaigns, webinars, trade shows, and other marketing activities
• Maintain accurate lead and opportunity information in CRM systems
• Develop knowledge of bioproduction products, workflows, customers, and sales processes
• Partner with Sales, Marketing, and technical teams to improve lead conversion and pipeline development
• Track biotech VC funding within the assigned territory and use funding events for prospecting and account development

Bioproduction Business Development Associate

Sales Development Rep

• Identify and develop new business opportunities
• Nurture customer relationships
• Provide innovative solutions across the portfolio of scientific products and services
• Work with cross-functional teams
• Leverage technologies to help customers advance research and improve healthcare outcomes
• Contribute to market growth and customer success
• Develop pipeline and generate leads
• Analyze market trends and provide competitive intelligence

Sales Development Representative II

Director

• Define and lead an innovation-driven service logistics strategy
• Align network design, digital tools, and operational execution to support MSD growth and service excellence
• Champion operational excellence across planning, distribution, transportation, and field logistics
• Drive digital transformation through automation, analytics, forecasting, and system integration
• Improve parts availability, reduce cycle time, and minimize instrument downtime
• Lead and develop a global team
• Partner with Manufacturing, Service, Planning, Quality, and Commercial teams
• Optimize the global logistics network, including distribution centers and forward stocking locations
• Establish performance metrics and dashboards
• Lead structured problem-solving and transformation initiatives
• Strengthen operational resilience through scenario planning, risk mitigation, and business-continuity strategies
• Communicate progress and priorities at the executive level
• Own budget and productivity targets while delivering efficiency gains

Director, Service Logistics

Physician

• Provide medical oversight of pharmacovigilance activities
• Ensure compliance with company SOPs, client directives, good clinical practice, and regulatory requirements
• Attend and present at sponsor meetings
• Provide medical and pharmacovigilance consultation to clients and project team members
• Support business development activities as needed
• Manage all medical aspects of contracted pharmacovigilance tasks across the pharmaceutical product life cycle
• Provide therapeutic and protocol training on assigned studies
• Write and/or review safety sections of CSRs, IND/NDA reports, ICSRs, signal detection reports, periodic reports, RMPs, REMS, and CTD modules
• Scientifically review aggregate reports, contribute to label updates, review literature, and support dossier maintenance and risk management activities
• Medically review cases and adverse events of special interest and serious adverse events
• Perform data reviews, including coding listings and full safety data, to assess potential safety concerns
• Review adverse event and serious adverse event data from solicited, spontaneous, and literature sources
• Identify and investigate safety signals
• Contribute to management of assigned products’ benefit-risk profiles

Pharmacovigilance Physician

Compliance

• Serve as lead over several countries/projects, providing regulatory expertise and client interface
• Review country-level essential documents for completeness, accuracy, and quality according to the study-specific Essential Document Compliance checklist
• Review site-level essential documents for completeness, accuracy, and quality
• Notify the EDP Submitter by email of review outcomes, requested revisions, and corrected documents when deficiencies are identified
• Review revised document packs to ensure deficiencies are resolved
• Communicate review outcomes to the SSU Specialist
• Track EDP review details in the applicable data tracking system
• Maintain knowledge of SOPs, client SOPs/directives, and current regulatory guidelines
• Support timely site activation

Senior Regulatory Affairs Specialist - FSP - EMEA

Inside Sales

• Generate sales growth through virtual and digital channels
• Build strong relationships with customers across academic, biotech, pharma, clinical and industrial markets
• Promote and sell Thermo Fisher Scientific's portfolio of scientific products and services
• Use consultative selling skills to understand customer needs and provide optimal solutions
• Develop and execute strategic sales plans
• Manage customer relationships through the CRM system
• Partner with cross-functional teams to achieve business targets

Inside Sales Account Manager – Biotech, French Speaking

• Lead global sales enablement and training, commercial operations, analytics, sales support, and related processes and systems
• Translate growth priorities into effective sales strategies and execution plans with CMD Commercial and BU Leadership
• Design and deploy global sales training, onboarding, and capability-development programs
• Develop sales enablement strategies, tools, and processes to improve seller productivity, pipeline conversion, and customer engagement
• Lead AI transformation across the commercial organization, including AI-enabled tools, automation, and insights
• Partner with Sales, IT, Digital, and other functions to accelerate adoption of AI capabilities
• Lead commercial analytics, dashboards, and performance management to improve forecasting and decision-making
• Strengthen CRM adoption, data quality, sales processes, and commercial technology capabilities
• Lead sales support and quote-to-order improvements
• Partner with Sales Compensation on sales incentive programs and annual quota targets
• Drive strategic commercial transformation and Practical Process Improvement (PPI) initiatives
• Build, lead, and develop a high-performing global team
• Partner cross-functionally with Sales, Marketing, Finance, Service, IT, HR, and Operations

Senior Director, Commercial Excellence

Clinical Research

• Perform and coordinate all aspects of clinical monitoring and site management
• Conduct remote and on-site visits to assess protocol and regulatory compliance
• Manage sponsor procedures, guidelines, and monitoring environments
• Ensure trials follow approved protocols, ICH-GCP guidelines, regulations, and SOPs
• Monitor investigator sites using a risk-based monitoring approach
• Apply root cause analysis to identify site process failures and corrective/preventive actions
• Ensure data accuracy through source document review, source data verification, and CRF review
• Assess investigational product inventory and records
• Document observations in reports and letters
• Escalate deficiencies and follow issues through resolution
• Maintain contact with investigative sites between monitoring visits
• Conduct monitoring tasks according to the approved monitoring plan
• Participate in investigator payments and investigator meetings
• Identify and initiate qualified clinical trial sites
• Perform trial closeout and retrieve trial materials
• Ensure essential documents are complete and conduct on-site file reviews
• Provide trial status and progress reports to the Clinical Team Manager
• Update clinical trial management systems
• Facilitate communication between sites, the client company, and the PPD project team
• Respond to company, client, and regulatory audits and inspections
• Complete expense reports and timesheets
• Assist with project publications, tools, process improvements, and other initiatives

Clinical Research Associate II/Sr CRA, Multiple Therapeutic Areas

Inspector

• Perform manual and/or automated visual inspection of finished or in-process pharmaceutical products, including vials, syringes, and bottles
• Identify and reject units with visual defects, including particulates, cracks, leaks, cosmetic defects, fill-volume abnormalities, labeling issues, and container-closure or integrity defects
• Record inspection results accurately in batch records, logbooks, or electronic systems
• Maintain data integrity by completing records legibly, contemporaneously, accurately, and according to GDP requirements
• Support investigations by providing inspection data, observations, and relevant information
• Perform basic inspection equipment checks and line clearance before use
• Maintain cleanliness and organization of inspection areas
• Report equipment malfunctions, environmental issues, quality concerns, and abnormalities promptly
• Package and transfer final products to the cold room
• Complete required training before performing assigned tasks
• Follow aseptic techniques and practices during aseptic operations
• Clean and maintain production equipment and classified manufacturing areas
• Transfer materials required for manufacturing batches
• Load and unload materials, equipment, or batches during production activities
• Perform stock checks of consumables and report material needs
• Follow safety, quality, EHS, business compliance, cGMP, and other compliance requirements
• Conduct in-process inspections and checks
• Load and unload vials at the tray loader station
• Perform assigned facility cleaning duties
• Carry out other duties assigned by the Manager

Visual Inspector II – 12 Hour Rotating Shift

• Perform and coordinate all aspects of clinical monitoring and site management
• Conduct remote and on-site visits to assess protocol and regulatory compliance
• Manage sponsor procedures and guidelines across different monitoring environments
• Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations and SOPs
• Ensure audit readiness and develop collaborative relationships with investigational sites
• Monitor investigator sites using a risk-based monitoring approach
• Apply root cause analysis to identify site process failures and implement corrective/preventive actions
• Ensure data accuracy through source document review, source data verification and CRF review
• Assess investigational product through physical inventory and records review
• Document observations in reports and letters and escalate deficiencies to clinical management
• Maintain contact with investigative sites between monitoring visits and follow up on issues
• Participate in investigator payment processes and findings resolution
• Participate in investigator meetings
• Identify potential investigators and initiate clinical trial sites
• Perform trial closeout and retrieve trial materials
• Ensure essential documents are complete and conduct on-site file reviews
• Provide trial status tracking and progress reports to the Clinical Team Manager
• Update study systems such as Clinical Trial Management Systems
• Facilitate communication between investigative sites, the client company and the PPD project team
• Respond to company, client and regulatory requirements, audits and inspections
• Complete expense reports and timesheets
• Assist with project publications and tools
• Contribute to project work and process improvement initiatives

Experienced Clinical Research Associate – CRA II, SR CRA

Supply Chain

• Develop and manage 24-month demand plans for key product portfolios
• Enhance forecast accuracy, optimize inventory levels, and ensure customer satisfaction
• Translate market insights into actionable supply chain plans
• Leverage advanced analytics and forecasting tools
• Manage Sales & Operations Planning (S&OP) processes
• Facilitate demand review meetings
• Implement continuous improvement initiatives
• Analyze market trends, historical data, and business intelligence to create accurate forecasts
• Maintain strong partnerships with Product Management, Commercial, Finance, and Manufacturing teams
• Optimize inventory levels, reduce excess and obsolescence risk, and ensure efficient production planning