Senior Process Engineer, Advanced Operations at Stryker

Portage, Michigan, United States

Stryker Logo
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Medical DevicesIndustries

Requirements

  • B.S in Mechanical Engineering or related engineering discipline with 2 or more years of relevant post-graduate experience
  • Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment
  • Excellent analytical skills, ability to plan, organize and implement concurrent tasks
  • Knowledge of manufacturing processes, materials, product and process design
  • Ability to read and interpret complex engineering drawings and understand geometrical dimensioning and tolerancing
  • Experience in an FDA regulated or regulated industry beneficial
  • Willingness to travel 20%

Responsibilities

  • Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with Stryker new product development procedures
  • Ensure quality of process and product as defined in the appropriate operation and material specifications
  • Assist in the selection of components and equipment based on analysis of specifications, reliability and regulatory requirements
  • Work with quality engineers to develop component specific testing and inspection protocols
  • Support capital acquisition activity from specifying equipment, contract negotiation, installation and validation
  • Analyze equipment to establish operating data, conduct experimental tests and result analysis
  • Lead and/or participate in process review meetings
  • Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches
  • Complete capability studies for in process inspection and generate subsequent inspection documentation
  • Conduct MSA studies for new products and new processes
  • Provide training for manufacturing team members
  • Ensure adherence to GMP and safety procedures
  • Review and approval of validation documentation

Skills

Mechanical Engineering
PFMEA
PPAP
MSA
GMP
SOP
Control Plan
Capability Studies
Process Validation
FMEA
Quality Engineering
Manufacturing Processes

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

Benefits

Medical & prescription plans
Supplemental health benefits
Flexible Spending accounts
Employee Assistance Program
Short-term & long-term disability
Tuition reimbursement
401(k) plan
Employee Stock Purchase Plan

Risks

Integration challenges from acquisitions may strain Stryker's resources.
Rapid tech advancements risk obsolescence of Stryker's current products.
Regulatory scrutiny on acquisitions could delay Stryker's market entry.

Differentiation

Stryker's acquisitions enhance its minimally invasive surgical solutions portfolio.
Entry into the peripheral vascular segment diversifies Stryker's market presence.
Stryker's focus on AI integration boosts diagnostic accuracy and operational efficiency.

Upsides

Growing demand for minimally invasive solutions aligns with Stryker's strategic acquisitions.
The orthopedic implants market growth benefits Stryker's expanding product line.
Stryker's acquisition of Inari Medical positions it in a high-growth vascular market.

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