Audit & Supplier Specialist

Work Schedule

Standard Office Hours (40/wk)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right

reasons - with the customer always on top of mind. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization

that values passion and outstanding contributions. Our dedication to our colleagues across the globe is to provide the resources and

opportunities they need to make a difference in our world while building an exciting and fulfilling career with us.

Location/division specific information:

We - the Thermo Fisher Scientific, Ferentino Site - are one of the leaders in manufacturing sterile liquid and lyophilized products. At

Ferentino, you will be part of a passionate Team which is dedicated to support a broad range of customers who are developing the treatments

and pharmaceuticals of the future.

Discover impactful work:

As part of the Quality Assurance Team you will assure the quality of current and future products and satisfy the very high expectations of our

customers in pharmaceutical manufacturing. You will achieve this by collaborating closely with other functions and departments to determine

solutions for diverse challenges as well as independently striving for continual improvement of Quality Management System processes.

A day in the life:

• Continually improve required Supplier Qualifications and Risk Management activities

• Contribute to the Quality Supplier Management activities

• Review, update and contribute to the development of site procedures

• Ensure Quality Agreements with clients are established and maintained

• Contribute to the site’s improvement and new projects introduction

Keys to success:

Education

• B.Sc. or M.Sc. in Pharmacy, Chemistry, Industrial Pharmacy or a related field.

• Further Qualifications in Quality Management or Quality Assurance encouraged

Experience

• Knowledge of Quality Management Systems with at least 2 years of experience

• Experienced in working in project teams

• Knowledge of directives (EU-GMP, US FDA 21 CFR)

Knowledge, skills, abilities

• Structured and very diligent working style including ability to organize yourself independently

• Analytical skills with proven ability to troubleshoot complex problems

• Strong interpersonal skills to work as a member of a team and collaborate effectively with other Teams and Functions

• Able to communicate clearly with internal and external partners regarding supplier management

• Good critical and logical thinking skills.

• Effective written, interpersonal, and presentation skills.

• Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint).

• Strong statistics knowledge and experience with Trackwise

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work

with us (https://jobs.thermofisher.com/global/en/5-reasons-to-work-at-thermo-fisher-scientific). As one team of 100,000+ colleagues, we share

a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific

challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse

experiences, backgrounds and perspectives are valued.