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(Senior) Process Engineer (m/f/d) Manufacturing (24 Months)

(Senior) Process Engineer (m/f/d) Manufacturing (24 Months)

(Senior) Process Engineer (m/f/d) Manufacturing (24 Months)

(Senior) Process Engineer (m/f/d) Manufacturing (24 Months)

Stryker

Medizintechnik

Tuttlingen

  • Art der Beschäftigung: Vollzeit
  • 65.000 € – 94.500 € (von XING geschätzt)
  • Vor Ort
  • Aktiv auf der Suche

(Senior) Process Engineer (m/f/d) Manufacturing (24 Months)

Über diesen Job

(Senior) Process Engineer (m/f/d) Manufacturing (24 Months)

Work flexibility: Hybrid Req ID: R554523 Employee type:
  • Temporary
  • Full Time
Job category: Engineering Travel: Relocation: No

Looking for a place that values your unique talents? Discover Stryker's award-winning culture.

We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

Job description

As a ( Senior) Process Engineer (m/f/d) you will oversee the seamless and timely transfer of products across multiple sites, with a strong emphasis on effective communication and coordination between Stryker’s sites. This role focuses on the engineering activities required to move production lines and ensure smooth operational transitions.

What you will do:

  • Provide engineering support for product transfers, ensuring all activities are completed and documented in accordance with the latest Stryker procedures.

  • Define the technical objectives of engineering assignments and make decisions regarding the direction and outcomes of these assignments.

  • Monitor and control the progress of work, ensuring the sound application of engineering principles and the proper use of policies and procedures.

  • Analyze equipment to establish operating data, conduct experimental tests, and interpret the results.

  • Participate in the creation of Validation, PFMEA, Control Plan, SOP, PPAP, and other Stryker internal process qualifications related to product transfers.

What you will need:

Required:

  • Bachelor’s degree in Engineering, Science, or a related field.

  • 2+ years of engineering experience within production / manufacturing in a highly regulated industry (medical devices, pharma, automotive, aerospace, food & beverage).

  • Knowledge of process/product validation, statistical methods, and process mapping.

  • Strong problem-solving skills in manufacturing/design technical issues.

  • Excellent English and German language skills, enabling seamless collaboration with local and global stakeholders.

Preferred:

  • Experience in medical device or manufacturing industries, ISO 13485, FDA 21 CFR Part 820, and global quality standards is nice to have.

We have signed the Diversity Charter and are proud to be part of this initiative to promote diversity in the workplace. Because diversity is important to us!
We welcome applications from people regardless of their ethnic, national, or social background, gender, disability, age, or sexual identity.

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Gehalts-Prognose

Unternehmens-Details

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Stryker

Medizintechnik

10.001 oder mehr Mitarbeitende

Freiburg im Breisgau, Deutschland

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