Lead mRNA Manufacturing
Lead mRNA Manufacturing
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Job Description
Work Schedule
Standard (MonFri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.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 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 distributed team 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.
ThermoFisher mRNA unit in Monza is looking for a Manufacturing Lead role!
As Lead in our mRNA Manufacturing Unit you will be responsible for supporting Operations Teams in planning and managing production activities during shifts ensuring adherence to all quality and regulatory control and documentation procedures according to schedule cost and quality standards.
You will have the chance to prove your leadership skills in a highly multifaceted and resultdriven environment.
What will you do
Managing the Manufacturing resources on shift and assigning/coordinating manufacturing and ancillary activities defining work priorities ensuring GMP Batches supply in a safe environment.
Supporting in coordinating operatives in daytoday operations making sure the production schedule and Right First Time and On Time Delivery KPIs are met.
Making sure that the production operations are controlled and regulatory compliance requirements are met by guaranteeing batch documentation is accurate Standard Operating Procedures are accurate critical documentation templates are accurate equipment is in good repair and current calibration and high standards of housekeeping are maintained in all areas of responsibility.
Acting as a point of contact with every internal function (MSAT PM Quality Supply Chain Maintenance) for any manufacturing / batch topics.
Supporting in handling anomalies and deviations solving production problems with the support of the MSAT Team Quality Operation and the Manufacturing Manager.
Ensuring high standards of safety and engagement amongst his team/shift.
Sharing business objectives and EHS information.
Education/ Experience
Preferred MS in the life sciences engineering or equivalent technical field.
5 years of experience in Pharmaceutical Manufacturing.
Knowledge Skills Abilities
Strong experience with GMP manufacturing.
Progressed experience in main Upstream (Media Preparation and Enzymatic reactions in Bioreactors) and in Downstream steps (TFF Chromatography Encapsulation Clarifications/Filtrations).
Good communication and leadership skills.
Proactive approach focus on prevention and problem solving.
Availability to work on shifts.
English and Italian.
Thermo Fisher Scientific is an Equal Opportunity Employer.
Join Us be part of our company that provides growth opportunities.
Employment Type
Full-Time
