An. Support Validation Technician

at  Thermo Fisher Scientific

20900 Monza, Lombardia, Italy -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate28 Nov, 2024Not Specified31 Aug, 2024N/AChromatography,SpectrophotometryNoNo
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Description:

JOB DESCRIPTION

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 complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
Monza DPD site is looking for an An. Support Validation Technician:
Joining the Analytical Support and Validation team in the QC Lab, you will be part of a multifaceted and result-driven environment and you will gain
and in-depth experience of a GMP Quality control lab focused on new projects, technology tranfers and cleaning validation.

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 drugs.
  • Learn to perform analysis effectively and in GMP compliance, mainly with 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, GC, UV…)
  • Excellent knowledge of Office Suite

Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.
Join Us

Responsibilities:

  • 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 drugs.
  • Learn to perform analysis effectively and in GMP compliance, mainly with manage and dispose samples preparing chemical solutions


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

20900 Monza, Italy