Equipment & Facilities Specialist at Charles River Laboratories
41564 Kaarst, Nordrhein-Westfalen, Germany -
Full Time


Start Date

Immediate

Expiry Date

09 Jul, 25

Salary

0.0

Posted On

06 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Infrastructure, Iso, Gmp

Industry

Information Technology/IT

Description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

REQUIRED SKILLS & EDUCATION:

  • Technical/scientific degree or completed vocational training in a technical/scientific field
  • Technical knowledge in the field of laboratory technology and/or building services engineering
  • Knowledge of project and quality management
  • Experience in the maintenance/servicing of equipment and infrastructure as well as qualification of equipment
  • Regulatory knowledge, especially in the area of ISO 9001 and GMP
Responsibilities
  • Manage areas and make them usable or optimize them for the respective requirements
  • Support order and cleanliness on site
  • Consumption management for the following areas: energy supply, gas supply, waste disposal
  • Continuous monitoring of compliance with legal requirements and economic efficiency
  • Repair or initiation of repairs in the event of equipment or building defects
  • Control and coordination of all operational support processes in the area of responsibility. This includes in particular maintenance and facility management
  • Ensuring the creation, review and maintenance of technical documentation
  • Assisting and advising employees on the qualification of devices and the validation of computerized systems, particularly with regard to regulatory and technical aspects
  • Creation and revision of the relevant SOPs for device qualification and validation of computerized systems
  • Device documentation taking into account the relevant SOPs
  • Advising departments on the selection of devices and the implementation of maintenance measures
  • Carrying out device qualification in accordance with applicable guidelines and relevant SOPs or advising other employees if qualification is not carried out in-house
  • SOP-compliant handling of all analyzers
  • Device responsibility for devices according to the current device list
  • Maintenance of the qualification master plan
  • Safety and health-conscious work in accordance with the relevant SOPs
  • Proper handling of the equipment
  • Preparation and support of audits by domestic and foreign customers / authorities / self-inspections and elimination of observations from inspections and audits
  • Advice and support in the design and planning of extension and conversion measures for the building and in compliance with the relevant guidelines as well as the coordination of the trades
  • Coordinating and monitoring the selection, commissioning and supervision of external service providers in the work area, including the acceptance of measures carried out
  • Creating and reviewing the relevant SOPs in the work area
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