Work Schedule Other
Environmental Conditions Office
Job DescriptionAt Thermo Fisher Scientific, you'll discover impactful work, innovative thinking, and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe, and delivering COVID-19 solutions. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions.
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, or improving patient health through diagnostics, we are here to support them.
The Monza DPD site is looking for a dedicated Coordinator, QC Equipment Calibration to provide additional value in the Quality Control Function.
Specific information – Discover impactful work:As QC Equipment Calibration Coordinator, you will join the QC Equipment Calibration team, working to guarantee the correct calibration and maintenance status of the QC laboratories equipment.
Your main duties will include:
Execution of daily calibration activitiesManagement of equipment calibration status, in compliance with GMP regulationsProvide support for analytical hardware and software related tasks, in compliance with logical security regulationsAssure accurate team-related documentation management, both in paper and electronic format, in compliance with GMP regulationsUsers training (internal and external)Participating in instrumental documentation issue and updateVendor management and activities supervisionWhereas needed, you will be involved in the following activities:
Management (creation/update/decommissioning) of documentation, such as Risk Assessment, CAPAs, Master Excel Spreadsheets, etc.Changes and deviations impact evaluation, and relevant action plans implementationEvaluation in purchasing/installation/dismission of equipment and in new projects reliabilityQC Equipment troubleshooting activitiesParticipation/Support for audit-related topicsKeys to Success:EducationUniversity degree (Chemical, CTF, or equivalent) or diploma with meaningful experience in this roleExperiencePrevious experience in a GMP pharmaceutical laboratory, or as a Supplier for Laboratory Equipment production companyKnowledge, Skills, AbilitiesGood English level (written and spoken)Knowledge of GLP/GMP regulationsKnowledge of analytical techniques, laboratory equipment, and related softwarePrecision and attention to detailCollaboration, self-organization, and good interpersonal skillsKnowledge of data management systems (e.g., Trackwise, Documentum) is helpfulWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.
Apply today! http://jobs.thermofisher.comThermo 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.
Do the difference and grow, join us!
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