Manufacturing Process Expert
Pubblicato il 05-10-2026 - Nessun nome in Monza
JOB DESCRIPTION
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
MAIN SCOPE OF THE POSITION/ RESPONSIBILITIES:
The Manufacturing Process Expert will serve as an advanced root cause analysis expert in support of a cross-functional team that is focused on problem-solving and continuous improvement for the site. The investigation team is a key part of the Technical Unit organization. It is focused on driving quality excellence, prevention of error and deviations, continuous improvement, and effective problem-solving. The Manufacturing Process Expert is responsible for facilitating and performing advanced root cause analysis to solve complicated technical problems and completed investigation.
ASSIGNMENTS, SPECIFIC/PRIMARY ACTIVITIES:
Investigations
Management of deviations, in collaborations with cross functional team
Investigation plan definition
Guide and/or execute the Root Cause Analysis for deviation events and guide the definition of CAPA with cross functional team
Execute Technical Analysis inside and outside the Technical Unit
Coordinate a cross functional investigation team inside and outside the Technical Unit i
Utilizes manufacturing process knowledge and investigation skills to identify and resolve manufacturing issues and drive continuous improvement in process operations
Technical process knowledge
Supports Manufacturing in the implementation of Corrective and Preventive actions (CAPA) in collaboration with Quality Specialist (QS).
Proactively identify and mitigate risks.
Sharing of lessons learned during the Technical Unit huddles
Audit
Utilizes manufacturing process knowledge and investigation skills during client and Regulatory audit for the deviation assigned
Methodology/KPI
Contribute to achieving "zero past due" objectives in Quality (CAPA, Deviations) within one's scope of responsibility, as well as RFT (Right First Time) and OTIF (On-Time In Full) objectives for document submission to the client and lot release.
RELATIONS:
Internal
All functions and seniority levels including Site Leadership Team
Supervisor Quality Manufacturing
TU assigned employees (operators, lead, team leaders, SPVs, tech team)
Quality Function
External
Corporate functions
Employees from other Thermo Fisher Scientific sites
Customers
Consulting firms
Suppliers
REQUIREMENTS
Degree in Chemistry/ CTF/ Biological Sciences or similar fields
Desirable
Experience in Quality Assurance Operations teams, with a focus on deviation management and support to GMP manufacturing Excellent knowledge of GMP and national/international regulations
Technical competences:
Necessary
Ability to function in a fast paced, dynamic environment with multiple priorities simultaneously.
Strong interpersonal and communications skills; written and oral.
Good knowledge of cGMP.
Must be skilled in meetings and interviews to eliciting technical details from subject matter experts.
Must be skilled in the use of a personal computer and related software applications, Trackwise strongly desired.
Ability to write, handle and review GMP documentation (Deviations, CAPAs...) and understanding of main quality indicators
Knowledge of injectable sterile process manufacturing
Desirable
Solid understanding of root cause analysis tools, TapRoot preferred.
Strong planning, organization and multitasking skills.
Good knowledge of TrackWise system
Professional Experience:
Necessary
Experience within manufacturing industries
Fluency in English and Italian