Req ID #: 226666
Kaarst, Nordrhein-Westfalen, DE
Full time
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
  About Microbial SolutionsOur Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.
  About Charles RiverCharles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
  With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.
  At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years.
  We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
  Equal Employment OpportunityCharles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.
  It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
  If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
  For more information, please visit www.criver.com

• 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