Info
Monza
Monza, Italy
Regular Full Time
Regular Full Time
Quality Control (QC), Analytical chemist, Molecular biology
Quality Control (QC), Analytical chemist, Molecular biology

This job offer is no longer active

Contact information is not publicly available anymore.

Biotech QC mRNA analyst

Inactive
Thermo Fisher Scientific - Career

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.

Biotech QC mRNA analyst

Work Schedule

7 1/2 hr shift

Environmental Conditions

Laboratory Setting

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 Biotech QC mRNA analyst

Joining the mRNA QC Lab, you will be included in a dynamic environment and you will gain and in-depth experience of a GMP Quality control lab passionate about new projects and technology transfers using your experience, you will specifically focus on the following tasks:

  • Perform analysis according to GMP rules on incoming, in-process and release samples to support mRNA processes in manufacturing
  • Implement documentation (protocols, reports, methods), ensuring their management according to current GMP, SOPs and guidelines;
  • Support instrument calibration, following SOPs and protocols.

Required skills and background:

  • Degree in Biotechnology / CTF or other Scientific field
  • Previous experience in laboratory is needed. Experience in a GMP QC lab is a plus.
  • Ability to perform common biotech and biochemical analysis: experience in PCR/qPCR, sequencing, ELISA, SDS-PAGE is strongly preferred. Experience in HPLC and CGE is a plus.
  • English and Italian languages (professional knowledge)
  • Good knowledge of Office Suite
 

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