Quality Vendor Management Specialist Monza

Quality Vendor Management Specialist
Monza
Lombardia, Monza

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 distributed team delivers an outstanding 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.

DPD Monza site is looking for a Quality Vendor Management Specialist!

Main tasks are:

Supplier audits:

Implementation of an annual plan for the execution of external audits at suppliers, aimed at verifying compliance with regulations and company requirements, and highlighting gaps to be filled, through the definition of corrective actions.

Quality agreement:

Support the manager in ensuring the implementation of the Quality Agreement with the supplier in compliance with current regulations (laws, European and international GMP regulations and company standards).

Supplier approval:

Ensure the approval of suppliers through the definition and updating of a supplier list in compliance with current regulations (laws, GMP regulations, FDA, etc.

).

Supplier Complaints:

Support the manager in ensuring the management of complaints to suppliers and reports to customers, in compliance with current regulations (laws, European and international GMP regulations and company standards) and in compliance with the deadlines agreed with Quality Operations.

Internal audits, Overlooker and F&F:

Ensure the regular carrying out of internal audits, overover and Fit & Finish inspections, through the planning and execution of assigned activities, the definition of corrective/preventive actions of the related responsibilities and implementation times, in order to allow the regular carrying out of the activities supervised by GMP, in compliance with current regulations (laws, GMP standards, FDA, etc. ).

Follow-up audit and management of corrective/preventive actions (CAPA)

Support the manager in ensuring the definition of adaptation actions to customer requests deriving from the audits, through the verification of consistency with current regulations, the definition of responsibilities and implementation times of corrective actions, the activation of active functions and the supervision of compliance with the times and requirements defined, in order to allow the acquisition of orders and to allow the regular carrying out of the activities established by GMP, in compliance with current regulations (laws, GMP standards, CFR 21, etc. )

customer indications, company interests.

Quality:

- a proactive approach

- team spirit

- a compliance oriented demeanor

- good knowledge of English

- sound expertise of IT tools (Office)

A consistent academic background (CTF, Biotech, Pharmaceutical studies) and previous experiences in a Pharmaceutical plant represent an important plus.

Thermo Fisher 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.

Join us!