Ingénieur projet / Process at Stryker

Grenoble, Auvergne-Rhone-Alpes, France

Apply Now

Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Manufacturing, Medical DevicesIndustries

Requirements

Expertise in at least one specific industrial manufacturing process on the site (e.g., machining, finishing, additive manufacturing)
Advanced technical skills as a Subject Matter Expert (SME) in industrial processes (e.g., machining, additive manufacturing, heat treatments)
Knowledge of risk analysis methods (pFMEA, AMDEC, HAZOP)
Familiarity with validation/qualification strategies for processes and equipment
Understanding of regulatory requirements and quality standards (ISO 13485, GMP, MDR, FDA)
Proficiency in project management (framing, planning, execution, monitoring, closure)
Ability to manage technical documentation (SOP, Work Instructions, PFMEA, control plans, validation protocols, ERP, COUPA)
Skills in technological watch and benchmarking of industrial best practices
Experience in failure analysis and problem resolution
Capacity to coordinate cross-functional teams (Production, Quality, R&D, AO, Maintenance, Purchases, Suppliers, Supply Planning)

Responsibilities

Structure and lead end-to-end projects for process optimization (framing, planning, execution, monitoring, closure)
Define project strategy, objectives, deliverables, performance indicators, and required resources
Manage risks and constraints associated with production processes
Monitor project progress, provide regular reporting, and ensure compliance with deadlines, budget, and quality requirements
Adapt projects to market challenges
Coordinate cross-functional teams for effective implementation of solutions
Identify and implement innovative solutions to improve process robustness, repeatability, and performance
Conduct technological watch and benchmark best industrial practices
Lead process risk analyses (pFMEA, AMDEC, HAZOP) and propose concrete improvement plans
Participate in failure analyses and problem resolutions with quality and production teams
Define and implement process and equipment qualification/validation strategies
Validate strategies with other SMEs for technical relevance and regulatory compliance
Organize and supervise tests, collect/analyze results, and draft validation deliverables
Ensure process compliance and robustness with regulatory and quality standards (ISO 13485, GMP, MDR)
Manage impact analyses of changes and define re-qualification actions
Update and continuously improve process documentation (SOP, Work Instructions, PFMEA, control plans, validation protocols, ERP, COUPA)
Ensure traceability and alignment of documentation with regulations and internal standards
Participate in internal and external audits as a process expert
Integrate technological and regulatory evolutions into technical documents
Provide training and share expertise on process optimization (technical and methodological)
Raise awareness among production teams on best practices and continuous improvement methodologies
Contribute to improving methods and practices in the Manufacturing Engineering department and support organizational changes
Pilot and coordinate process optimization projects
Make decisions on technical improvements

Skills

Key technologies and capabilities for this role

Project ManagementProcess OptimizationMachiningAdditive ManufacturingHeat TreatmentpFMEARisk ManagementCross-functional CoordinationTechnical DocumentationTechnological Benchmarking

Questions & Answers

Common questions about this position

Is this position remote or onsite?

The position requires onsite work.

What is the salary or compensation for this role?

This information is not specified in the job description.

What key skills are required for the Ingénieur Projet/Process role?

The role requires expertise in specific industrial processes like machining, additive manufacturing, or finishing; project management skills including planning, risk management, and cross-functional coordination; and knowledge of process validation, regulatory compliance (ISO 13485, GMP, MDR), and risk analyses (pFMEA, AMDEC, HAZOP).

What does the team collaboration look like in this role?

The role involves coordinating transverse teams including Production, Quality, R&D, AO, Maintenance, Purchases, Suppliers, and Supply Planning to implement solutions effectively.

What makes a strong candidate for this position?

A strong candidate is an expert (SME) in at least one specific industrial process, with proven project leadership from scoping to closure, skills in innovation and process optimization, and experience in validation strategies and regulatory compliance.

Stryker

Develops and manufactures medical devices and equipment

About Stryker

Stryker develops and manufactures medical devices and equipment aimed at improving patient care and surgical efficiency. Their products include surgical tools, neurotechnology devices, and orthopedic implants, which are sold directly to hospitals and clinics. Stryker stands out from competitors by focusing on high-quality products and a commitment to advancing healthcare solutions. The company's goal is to enhance the overall healthcare experience for both patients and medical professionals.

Kalamazoo, MichiganHeadquarters

1941Year Founded

$423.3MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees