Senior COMOS Analyst and CSV Professional
at Thermo Fisher Scientific
Lengnau, BE, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 09 Feb, 2025 | Not Specified | 10 Nov, 2024 | N/A | Good communication skills | No | No |
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Description:
ABOUT THERMO FISHER SCIENTIFIC
As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.
Job Description
- Act as the administrator of our plant engineering software COMOS. As part of this function you will:
- provide level 1 and 2 support for all users and performs user management.
- act as a coordinator between the vendor Siemens and COMOS key users for all topics related to COMOS.
- handle change controls for COMOS and take responsibility in implementing and validating these changes detailed.
- write and review lifecycle documents for COMOS, ensuring they meet our especially high standards.
- Act as validation responsible for all electronic laboratory systems used in the QC department.This includes the creation and review of validation documents such as risk assessments, validation plans, and reports, as well as ensuring the validated status of the systems.
- Act as GMP delegate for the Execution Systems team to check, monitor, and report the status of change control records.
- Deputize for the Manager CSV Lengnau.
Your qualification
- 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 determine the 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 diverse teams.
- Proficiency in English. German is a plus.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Engineering
Proficient
1
Lengnau, BE, Switzerland