Chem QC mRNA Analyst

at  Thermo Fisher Scientific

20900 Monza, Lombardia, Italy -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Jul, 2024Not Specified18 Apr, 20243 year(s) or aboveTechnology Transfer,Spectrophotometry,ChromatographyNoNo
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Description:

JOB DESCRIPTION

Thermo Fisher Scientific Inc. is the world leader in serving science. 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 unrivaled 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.
mRNA BU is looking for a Chemical QC Technician.
Joinin the mRNA Quality Control Laboratory, with focus on chemical tests, you will specifically support the mRNA manufacturing department.

You will be part of a dynamic and result-driven environment and you will gain and in-depth experience of a GMP QC lab focused on new projects, technology transfer and cleaning validation activities (i.e. cleaning method validation, sampling activities in manufacturing area, analyses of the samples collected). With 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.
  • Provide testing support for production of sterile injectable drugs.
  • Learn to perform analysis effectively and in GMP compliance, mainly with chromatography and spectrophotometry.
  • Run and dispose samples preparing chemical solutions.

How you will get there?

  • At least 3 years of experience in a GMP Quality Control Chemical Laboratory;
  • Ability to perform common chemical analysis, experience in chromatography and spectrophotometry;
  • Ability to develop, transfer, validate analytical methods;
  • Knowledge of fragment analysis techniques such as Capillary Gel Electrophoresis (CGE) is a plus;
  • Strong knowledge of the main chemical techniques (HPLC, GC, UV, TOC…);
  • Focus on timelines and on time completion;
  • Ability to work independently and as a member of a cross-functional team;
  • English and italian languages (professional knowledge);
  • Excellent knowledge of Office Suite.

ThermoFisher 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.
  • Provide testing support for production of sterile injectable drugs.
  • Learn to perform analysis effectively and in GMP compliance, mainly with chromatography and spectrophotometry.
  • Run and dispose samples preparing chemical solutions


REQUIREMENT SUMMARY

Min:3.0Max:8.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

20900 Monza, Italy