Supervisor Quality Control Mrna - Monza, Italia - Thermo Fisher Scientific

Thermo Fisher Scientific
Thermo Fisher Scientific
Azienda verificata
Monza, Italia

1 settimana fa

Piero Bianchi

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee


Descrizione
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 global 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 Supervisor for QC


Joining the mRNA QC Lab, you will join a dynamic and result-oriented atmosphere and you will gain and in-depth experience of a GMP Quality control environment, passionate about new projects and new technologies.


The Supervisor of Quality Control (QC) mRNA provides leadership, scientific, compliance and technical expertise for all QC activities at the mRNA QC lab within the Monza, Italy site.

These activities include the
readiness of the GMP materials needed for manufacturing of clinical and commercial bio-pharmaceuticals and the managing the
microbiology analytical activities.

This will be achieved by scheduling activities of the team.

How will you get there?

  • Master degree in Life Sciences or Chemical/Biological Engineering
  • Ability to use pharmacopeia monographs and global pharmacopoeia (mainly EP/USP) to compendial incoming materials.
  • Have a solid understanding and experience with cGMP FDA, EMEA and ICH regulatory requirements.
  • Experience in a QC GMP Laboratory, including documentation, reports, and exceptions.
  • Should understand scientific aspects of modern laboratory, environmental monitoring and microbiology procedures.
  • Experience with Gene Therapy / Plasmid DNA / mRNA products preferred.
  • Experience in a quality control position within the biological and/or pharmaceutical industry (or combination of an advanced degree and quality experience).

Requested soft skills and abilities:
Ability to plan and organize are must have abilities.

Planning analytical activities in order to guarantee the respect of the timelines agreed internally and with Clients, always maintaining high quality levels and GMP standards.


Supervisory experience and team management skill: coordinate the team, giving value to positive results and evaluating the need of training and development.

Commitment and high motivation are the goals

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.

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