System Administrator for COMOS and CSV
vor 1 Woche
About Thermo Fisher Scientific:
We are a world leader in serving science, with an industry-leading scale that means unparalleled commercial reach and outstanding customer access. Our broad customer base spans from research to clinical to commercial production, offering you the opportunity to have a broad and relevant impact.
Job Description:
As a System Administrator for COMOS and CSV, you will be responsible for providing level 1 and 2 support for all users and performing user management. You will also act as a coordinator between Siemens and COMOS key users for all topics related to COMOS, handle change controls, and take ownership of implementing and validating these changes. Additionally, you will write and review lifecycle documents for COMOS, ensuring they meet our high standards. As a validation responsible, you will create and review validation documents, such as risk assessments, validation plans, and reports, and ensure the validated status of electronic laboratory systems used in the QC department. Finally, you will act as a GMP delegate to check, monitor, and report the status of change control records.
Responsibilities:
* Provide level 1 and 2 support for all users and perform user management
* Act as a coordinator between Siemens and COMOS key users for all topics related to COMOS
* Handle change controls and take ownership of implementing and validating these changes
* Write and review lifecycle documents for COMOS, ensuring they meet our high standards
* Create and review validation documents, such as risk assessments, validation plans, and reports
* Ensure the validated status of electronic laboratory systems used in the QC department
* Act as a GMP delegate to check, monitor, and report the status of change control records
Requirements:
* Bachelor's or Master's degree in engineering or life sciences
* Experience in the pharmaceutical industry
* Experience as a COMOS administrator or similar role
* Strong background in CSV (Computer System Validation) and GMP (Good Manufacturing Practices)
* Ability to resolve best course of action for system validation and support
* Outstanding skills in crafting and reviewing technical documentation
* Ambitious and able to strictly adhere to internal and health authority validation and quality standards
* Excellent communication and collaboration skills to work seamlessly with complementary teams
* Proficiency in English; German is a plus
Salary: $80,000 - $110,000 per year
Benefits:
* Competitive salary and benefits package
* Opportunity to work in a dynamic and innovative company
* Collaborative and supportive team environment
* Professional development and growth opportunities
Thermo Fisher Scientific is an EEO/Affirmative Action Employer
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