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CBRE Quality & Compliance Specialist in Luzern, Switzerland

Quality & Compliance Specialist

Job ID

186559

Posted

27-Sep-2024

Service line

GWS Segment

Role type

Full-time

Areas of Interest

Facilities Management

Location(s)

Luzern - Luzern - Switzerland

CBRE Global Workplace Solutions provides integrated facility management services on all continents with more than 60,000 employees. In Switzerland, the GWS division provides technical, infrastructural and commercial facility management services for clients from various industries.

For our growing Facility Management organization at a client in the Life Science sector in Schachen (LU) we are looking for a:

Quality & Compliance Specialist (m/w/d) 100%

Your main tasks:

•Document and reports on quality topics presented at daily site meetings

•Lead investigations, technical follow-ups / root cause investigations and initiating corrective and preventive measures

•Creation and revision of standard operating procedures and service level agreements between the client and CBRE

•Support of the Facility Management department in quality and compliance issues

•Support of the site manager in the preparation of monthly and quarterly figures and reports

•Support with audit and inspection requirements

•Work to site specific quality goals and objectives and measured through defined KPI’s

•Support and Partner with the Facility Management department in quality and compliance issues

•Support and participates in continuous improvement of Quality and Compliance for CBRE

•Appropriately escalates and notifies CBRE and client management of quality and compliance issues

•Support GxP compliance and qualification of all regulated service vendors

•Develops, motivate, and direct team members and foster a team environment

•Preforms other duties as assigned

•Leads by example and models behaviours that are consistent with the company's values

Your profile:

•Completed studies in the scientific or technical field biology, Microbiology, Chemistry, or Engineering; or equivalent related work experience

•Several years’ experience in a pharmaceutical research/manufacturing quality organization

•cGMP experience in the chemical, pharmaceutical, biotech, medical device, or food industry is preferable

•Analytical and logical thinking, flexible and precise way of working

•Willing to expand and pass on technical know-how internally and externally

•Fluent German and English skills

•Quality auditing experience preferable

•Experience with Desktop publishing, Microsoft Office Suite, and Online Help. Previous experience with SAP, Track wise, Regulus, and/or CMMS systems preferable

What we can offer you:

•Open and innovative working environment with design options

•Regional and international development opportunities in a fast-growing company

•Wide range of internal and external training opportunities

•CBRE GWS as a global player in the service sector with well-known customers from a multinational environment

•Good framework conditions, such as at least five weeks of vacation, 40 hours a week, as well as an attractive pension fund solution.

Contact: Edwin Murray, Talent Acquisition Partner, +41 79 501 50 93

We look forward to receiving your application!

CBRE, Inc. is an Equal Opportunity and Affirmative Action Employer (Women/Minorities/Persons with Disabilities/US Veterans)

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