Manufacturing Systems and Project Leader Job at Danaher Corporation (Cardiff)

Lean Manufacturing Leader (Omex Plant Leader)

The OMEX Leader drives the implementation of Ontex Manufacturing Excellence (OME...

Location

Mexico , Tijuana

Salary:

Not provided

Ontex Peninsular

Expiration Date

Until further notice

Requirements

Strong organizational and communication skills
team player with a positive, flexible, and proactive mindset
Solid project management skills (initiation, planning, execution, and delivery)
Strong analytical and critical thinking capabilities, with a data-driven approach to value creation
Proven coaching, influencing, training, and facilitation skills across different organizational levels
Strong change management capabilities and problem-solving mindset
Experience leading teams to achieve ambitious goals
Ability to manage stakeholders across multiple levels of the organization
Knowledge of Lean Management Systems is highly desirable
Comfortable working in a fast-paced, dynamic, test-and-learn environment

Job Responsibility

Build credibility and engagement around the Ontex way of working through strong on-the-floor presence and leadership
Coach and support departments in the implementation of OMEX systems, proactively identifying and escalating roadblocks
Lead the development and deployment of the site vision using the OGSM methodology, aligned with business objectives and supported by OMEX experts
Drive capability building, especially for system owners, and promote effective implementation of PDCA cycles
Lead and role-model loss elimination methodologies to solve technical and organizational problems
Ensure standardization within the plant and alignment with the broader Ontex network
Act as the plant’s OMEX subject matter expert, continuously developing own capabilities
Mentor employees in tools and methodologies, ensuring strong KPI/API linkage and sustainable results
Ensure training effectiveness and alignment of tools with job roles and responsibilities
Own and drive operational routines (daily, weekly, and management reviews), including benchmarking practices

Fulltime

Sr Project Leader

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

United States , Skaneateles Falls

Salary:

104000.00 - 143000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Proven project management experience leading cross-functional teams in product development environments
Experience supporting software-intensive products, SaMD, and/or regulated medical device hardware development
Working knowledge of Agile Scrum principles and the ability to facilitate Scrum ceremonies within a regulated environment
Understanding of medical device development regulations and standards (e.g., FDA design controls, ISO 13485, IEC 62304, ISO 14971), or experience in other highly regulated industries
Demonstrated ability to influence team members, manage priorities, and drive execution against challenging timelines
Strong interpersonal and communication skills with the ability to engage diverse technical and functional stakeholders
Solid business acumen with experience managing project budgets, resources, and trade-off decisions
4+ years of experience in project management or leading new product development teams, including coordination with external partners or suppliers
Bachelor’s degree in a technical discipline required
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time

Job Responsibility

Lead cross-functional, multidisciplinary teams—potentially including globally distributed resources—in the development of Software and/or medical device hardware products
Plan and execute projects in alignment with New Product Development (NPD), Design Control, and Quality Management System requirements
Collaborate with software, systems, hardware engineering, quality, regulatory, manufacturing, and supply chain partners to develop and maintain integrated project plans
Facilitate tasks, responsibilities, and accountability to team members to achieve project and product objectives
Facilitate Agile Scrum processes for projects, including sprint planning, daily standups, sprint reviews, and retrospectives, while ensuring alignment with regulated development practices
Drive achievement of project milestones related to quality, time-to-market, cost, and regulatory compliance
Track and manage project budgets, including labor, operating expenses, and capital expenditures
Monitor project status, risks, and dependencies
apply appropriate change management practices to evaluate and address schedule, scope, or resource variances
Coordinate and support assessments of scope changes and their impact to quality, regulatory, cost, and schedule commitments

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Sr Project Leader

The Sr Project Leader will lead cross-functional teams in the execution of Medic...

Location

United States , Skaneateles Falls

Salary:

104000.00 - 143000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Proven project management experience leading cross-functional teams in product development environments
Experience supporting software-intensive products, SaMD, and/or regulated medical device hardware development
Working knowledge of Agile Scrum principles and the ability to facilitate Scrum ceremonies within a regulated environment
Understanding of medical device development regulations and standards (e.g., FDA design controls, ISO 13485, IEC 62304, ISO 14971), or experience in other highly regulated industries
Demonstrated ability to influence team members, manage priorities, and drive execution against challenging timelines
Strong interpersonal and communication skills with the ability to engage diverse technical and functional stakeholders
Solid business acumen with experience managing project budgets, resources, and trade-off decisions
4+ years of experience in project management or leading new product development teams, including coordination with external partners or suppliers
Bachelor's degree in a technical discipline required

Job Responsibility

Lead cross-functional, multidisciplinary teams—potentially including globally distributed resources—in the development of Software and/or medical device hardware products
Plan and execute projects in alignment with New Product Development (NPD), Design Control, and Quality Management System requirements
Collaborate with software, systems, hardware engineering, quality, regulatory, manufacturing, and supply chain partners to develop and maintain integrated project plans
Facilitate tasks, responsibilities, and accountability to team members to achieve project and product objectives
Facilitate Agile Scrum processes for projects, including sprint planning, daily standups, sprint reviews, and retrospectives, while ensuring alignment with regulated development practices
Drive achievement of project milestones related to quality, time-to-market, cost, and regulatory compliance
Track and manage project budgets, including labor, operating expenses, and capital expenditures
Monitor project status, risks, and dependencies
apply appropriate change management practices to evaluate and address schedule, scope, or resource variances
Coordinate and support assessments of scope changes and their impact to quality, regulatory, cost, and schedule commitments

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Sr Project Leader

The Sr Project Leader will lead cross-functional teams in the execution of Medic...

Location

United States , Skaneateles Falls

Salary:

104000.00 - 143000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Proven project management experience leading cross-functional teams in product development environments
Experience supporting software-intensive products, SaMD, and/or regulated medical device hardware development
Working knowledge of Agile Scrum principles and the ability to facilitate Scrum ceremonies within a regulated environment
Understanding of medical device development regulations and standards (e.g., FDA design controls, ISO 13485, IEC 62304, ISO 14971), or experience in other highly regulated industries
Demonstrated ability to influence team members, manage priorities, and drive execution against challenging timelines
Strong interpersonal and communication skills with the ability to engage diverse technical and functional stakeholders
Solid business acumen with experience managing project budgets, resources, and trade-off decisions
4+ years of experience in project management or leading new product development teams, including coordination with external partners or suppliers
Bachelor's degree in a technical discipline required
Experience in one or more of the following areas is preferred: software development, systems engineering, electronics, mechanical design, injection-molded plastics, requirements management, verification and validation, or testing

Job Responsibility

Lead cross-functional, multidisciplinary teams—potentially including globally distributed resources—in the development of Software and/or medical device hardware products
Plan and execute projects in alignment with New Product Development (NPD), Design Control, and Quality Management System requirements
Collaborate with software, systems, hardware engineering, quality, regulatory, manufacturing, and supply chain partners to develop and maintain integrated project plans
Facilitate tasks, responsibilities, and accountability to team members to achieve project and product objectives
Facilitate Agile Scrum processes for projects, including sprint planning, daily standups, sprint reviews, and retrospectives, while ensuring alignment with regulated development practices
Drive achievement of project milestones related to quality, time-to-market, cost, and regulatory compliance
Track and manage project budgets, including labor, operating expenses, and capital expenditures
Monitor project status, risks, and dependencies
apply appropriate change management practices to evaluate and address schedule, scope, or resource variances
Coordinate and support assessments of scope changes and their impact to quality, regulatory, cost, and schedule commitments

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

R&D Project Leader

Location

Italy , Follina

Salary:

Not provided

Ariston

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Engineering or a related technical field
5–10 years of experience in mechanical design and product development, preferably in an industrial/manufacturing environment
Strong expertise in mechanical design, materials, and manufacturing processes
Proven experience with CAD tools (e.g., SolidWorks) and product data management systems
Demonstrated ability to manage projects, prioritize activities, and meet deadlines with a high degree of autonomy
Strong problem-solving mindset with a structured and analytical approach
Excellent stakeholder management and communication skills
Proactive, results-driven, and able to thrive in a dynamic environment
Proficiency in Italian and English is a must

Job Responsibility

Lead the design and development of components (e.g., plastic and metal parts) and complex assemblies, ensuring performance, manufacturability, and cost-efficiency
Own the end-to-end product development lifecycle, from concept and feasibility studies to industrialization and release
Use advanced parametric design tools (e.g., SolidWorks) to create and validate 2D/3D models, simulations, and technical documentation
Manage and optimize Bills of Materials (BOM), ensuring accuracy, cost control, and alignment with project requirements
Apply in-depth knowledge of industrial manufacturing processes (e.g., injection molding, machining, assembly) to drive design-for-manufacturing (DFM) and design-for-assembly (DFA) principles
Collaborate with internal project stakeholders (e.g., R&D, laboratory, quality, product management, operations) to ensure alignment on project objectives and milestones
Lead technical interactions with suppliers, including co-design activities, feasibility assessments, and issue resolution
Ensure compliance with company standards, technical specifications, and regulatory requirements

Project Leader

The Labeling Project Leader is responsible for leading multiple projects within ...

Location

Malta , San Ġwann

Salary:

32000.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Customer minded with good interpersonal and communication skills and the ability to interact effectively with all levels of local and international organization
Proficient use of Microsoft Office (Word, PowerPoint, Excel, OneNote, SharePoint)
Experience understanding project schedules, Microsoft Project a plus
Understanding of labeling, translation, change control processes and data management systems helpful
Experience with global cross-functional team meetings
Knowledge of change management systems preferred

Job Responsibility

Responsible for owning, managing and monitoring multiple simple to moderate labeling projects from initiation through completion
Develops and writes a project scope summary description and rationale based on the labeling request’s scope and requirements
Determine execution strategy in change management system
Develop change plans activities and monitor activity closure
Create and manage schedules to track projects to service level agreements
Interact with global manufacturing plants to implement labeling on product
Collaborate with global stakeholders to drive projects to completion
Facilitate meetings to resolve project conflicts
Monitor and control projects throughout the project lifecycle to mitigate and eliminate risks, resolve issues, schedule delays and resource constraints
The incumbent will perform other duties as assigned

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Project Leader

The Labeling Project Leader is responsible for leading multiple projects within ...

Location

Malta , San Ġwann tal-Għargħar

Salary:

32000.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Experience in a global environment in pharmaceutical labeling or regulated industries preferred
Customer minded with good interpersonal and communication skills and the ability to interact effectively with all levels of local and international organization
Proficient use of Microsoft Office (Word, PowerPoint, Excel, OneNote, SharePoint)
Experience understanding project schedules, Microsoft Project a plus
Understanding of labeling, translation, change control processes and data management systems helpful
Experience with global cross-functional team meetings
Knowledge of change management systems preferred

Job Responsibility

Responsible for owning, managing and monitoring multiple simple to moderate labeling projects from initiation through completion
Develops and writes a project scope summary description and rationale based on the labeling request’s scope and requirements
Determine execution strategy in change management system
Develop change plans activities and monitor activity closure
Create and manage schedules to track projects to service level agreements
Interact with global manufacturing plants to implement labeling on product
Collaborate with global stakeholders to drive projects to completion
Facilitate meetings to resolve project conflicts
Monitor and control projects throughout the project lifecycle to mitigate and eliminate risks, resolve issues, schedule delays and resource constraints
The incumbent will perform other duties as assigned

What we offer

Apoyo a las padres
Educación continua/ Desarrollo profesional
Salud de los empleados y Beneficios de bienestar
Tiempo libre pagado
2 días al año para ser voluntario

Quality Systems Leader

As a Quality Systems Leader, you will coordinate and improve the Quality Managem...

Location

Mexico , San Juan del Río

Salary:

Not provided

PPG Industries

Expiration Date

Until further notice

Requirements

Bachelor of Science degree in a related field, or equivalent experience
+ 3 years of experience in a quality role within a manufacturing environment
automotive industry experience
IATF-16949 Lead Auditor certification
Solid knowledge of quality management systems (IATF-16949, ISO 9001), document control, and automotive "Core Tools" (APQP, PPAP, FMEA, and SPC)
Experience with QMS (Quality Management Systems) software
Fluent English

Job Responsibility

Manage the document control system, including the development, initial release, and revision of all QMS documents and SOPs
Create, schedule, and conduct internal audits to ensure the QMS complies with IATF-16949 and other relevant standards
Manage the tracking of internal and external corrective actions, assisting teams in their investigation and closure
Be an important liaison and provide support during customer and third-party certification audits
Review deviation report trends to identify areas for systemic improvement
Assist the Quality Systems Manager in accomplishing quality projects
Ensure successful integration of all quality systems with the QMS
Analyze quality data to identify trends and suggest process improvements to increase compliance and efficiency
Review and monitor the implementation of specific customer requirements to ensure they are integrated into the QMS

Fulltime

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Manufacturing Systems and Project Leader

Job Description

Job Responsibility

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