Analytical Support Validation Technician
Analytical Support Validation Technician
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Job Description
Work Schedule
7 1/2 hr shiftEnvironmental Conditions
Laboratory SettingJob Description
Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue of approximately $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 growing efficiency in their laboratories improving patient health through diagnostics or the development and manufacture of lifechanging therapies we are here to support them. Our global organization of more than 100000 colleagues delivers an outstanding combination of innovative technologies purchasing convenience and pharmaceutical services through our industryleading brands including Thermo Scientific Applied Biosystems Invitrogen Fisher Scientific Unity Lab Services Patheon and PPD.
Monza site is an outstanding pharmaceutical contract manufacturing and development facility specialized in aseptic injectable with an increasing focus on biologics. Joining more than 1800 colleagues on site the selected candidate will experience an excellent international and fastgrowing environment. With revenues exceeding $24 billion and the largest investment in R&D in the industry we give our people the resources and chances to create meaningful contributions to the world.
Joinin the Analytical Support and Validation team you will be part of a dynamic and resultdriven environment and you will gain and indepth experience of a GMP Quality control lab focused on new projects and technology transfers. Leveraging your experience with chromatography and spectrophotometry you will specifically focus on the following tasks:
Support in the implementation of protocols reports and documents and ensure their management according to current GMP SOPs and guidelines.
Perform analyses following specified instructions from team leader and supervisor SOPs and analytical procedures.
Perform other duties and support activities as assigned be compliant with all job related safety and other training requirements.
Provide testing support for production of sterile injectable .
Learn to perform analysis effectively and in GMP compliance.
Manage and dispose samples preparing chemical solutions.
How you will get there
Qualifications
Previous experience in a GMP Quality Control lab
Ability to perform common chemical analysis experience in chromatography and spectrophotometry is strongly preferred
English and italian languages (professional knowledge)
Knowledge of the main chemical techniques (HPLC TOC UV...
Excellent knowledge of Office Suite
Required Experience:
IC
Employment Type
Full-Time
