Engineer (m/f/d) Medical Technology/Mechanical Engineering/Electrical Engineering

CRConsultants GmbH; Lübeck; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Benefits dieser Stelle

Team events

Training days

Subsidized sports program

Flexible working hours

Defined bonus concept

Zusammenfassung

CRConsultants GmbH in Lübeck is seeking an Engineer (m/f/d) specializing in Medical Technology, Mechanical Engineering, or Electrical Engineering. You will manage process changes for medical device manufacturers and ensure compliance with regulatory requirements.

Your role involves preparing essential documentation, actively participating in validations, and maintaining quality management systems. Employees benefit from a structured salary and bonuses, as well as team events and flexible working arrangements.

Qualifikationen

• Experience managing process changes at medical device manufacturers.
• Ability to prepare production-related documentation for product approval.
• Familiarity with maintaining regulatory compliance in medical technology.

Aufgaben

• Manage process changes at medical device manufacturers.
• Prepare production-related documentation for product approval.
• Support in performing validations and qualifications for new devices.

Kenntnisse

Technical understanding

Knowledge of regulatory compliance

Project management

Jobbeschreibung

Engineer (m/f/d) Medical Technology/Mechanical Engineering/Electrical Engineering

Do you love driving forward diverse projects and want to help make the world a safer place? By implementing regulatory requirements in technical processes, we support our customers on their journey toward safe products and processes.

With a good mix of technical understanding and enjoyment of working with people, you will help our customers understand new or modified manufacturing processes, evaluate their robustness, optimize them, and thereby ensure safe and efficient manufacturing processes. In addition to these tasks, you will impart knowledge about the compliance processes that secure these manufacturing processes from a regulatory perspective.

customer relationship

Technical expertise

Your responsibilities

• Management of process changes at medical device manufacturers
• Preparation of production-related documentation for product approval
• Working on projects to maintain regulatory compliance in the medical technology sector
• Support in performing validations and qualifications for the commissioning of new devices and machines
• Preparation of operating instructions, hazardous substance instructions, and job safety analyses
• Implementation and maintenance of quality management systems.

What benefits we offer

Team Events

To boost team spirit, we plan events for the entire team twice a year and an after-work get-together every month.

Trainingdays

Every quarter, we have a team day with the entire team and continue our training.

CRCare

Our subsidized sports program for fitness and health, as well as bike leasing for private use

CRC LifeTime

A working time account model for the optimal combination of professional and personal goals, as well as flexible working hours and mobile office

CRC Feelgood

Our Feelgood Manager always has an open ear for the wishes of the team and each individual.

salary structure

A clear salary structure and a defined bonus concept for every employee