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Team Leader, Sterile Area
Team Leader, Sterile Area-July 2024
Arcore
Jul 29, 2026
ABOUT THERMO FISHER SCIENTIFIC
As the world’s leader in serving science, at Thermo Fisher Scientific, our professionals develop critical solutions—and build rewarding careers.
10,000+ employees
Biotechnology, Manufacturing
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About Team Leader, Sterile Area

  Job Description

  Thermo Fisher Scientific, Pharma Service, plant in Monza is an elite contract manufacturing facility, specialized in aseptic injectable drugs. Joining 2000 colleagues on site, the selected candidate will experience a smart, driven, and fast-growing environment.

  With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make meaningful contributions to the world.

  As Team Leader in of our Sterile Filling you will be responsible for supporting the team in planning and leading production activities during shifts, ensuring adherence to all 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 result-driven environment. This role will give you an unmatched experience with aseptic fill and finish process and the experience in people management will be an invaluable asset for your next career step in Thermo Fisher Scientific!

  Key tasks

  Leading the Sterile Area Operators on shift, assigning activities and acting as a point of contact with every internal function (Quality, Maintenance...)Support in coordinating operatives in day to day operations, making sure that production schedule, Right First Time and On Time Delivery KPIs are met.Support in managing anomalies and deviations, solving production problems with the support of the department head.Ensure high standards of safety and engagement amongst his team/shiftMake sure that the Sterile production operations are properly 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.

  Qualifications:

  Degree's in CTF, Chemistry, Biology or relevant on the job experienceMore than 1 year of experience with GMP manufacturing, experience with aseptic fill & finish process is strongly preferredGood communication and proactive approach, focus on prevention and problem solvingEnglish and ItalianAvailability to work on shifts

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