Analytical Support Validation Technician

Work Schedule

7 1/2 hr shift

Environmental Conditions

Laboratory Setting

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $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 sophisticated 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 global organization of more than 100,000 colleagues 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.

The Monza site is an outstanding pharmaceutical contract manufacturing and development facility, specialized in aseptic injectable drugs, with an increasing focus on biologics. Joining more than 1800 colleagues on site, the selected candidate will experience an excellent, international, and fast-growing environment. With revenues exceeding $24 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create meaningful contributions to the world.

Joining the Analytical Support and Validation team, you will be part of a dynamic and result-driven environment and you will gain in-depth experience of a GMP Quality control lab focused on new projects and technology transfers. Leveraging your experience with chromatography and spectrophotometry, you will specifically focus on the following tasks:

1. Support in the implementation of protocols, reports, and documents and ensure their management according to current GMP, SOPs and guidelines.
2. Perform analyses following specified instructions from team leader and supervisor, SOPs and analytical procedures.
3. Perform other duties and support activities as assigned, being compliant with all job-related safety and other training requirements.
4. Provide testing support for production of sterile injectable drugs.
5. Learn to perform analysis effectively and in GMP compliance.
6. Manage and dispose of samples preparing chemical solutions.

How you will get there?

Qualifications

1. Previous experience in a GMP Quality Control lab.
2. Ability to perform common chemical analysis; experience in chromatography and spectrophotometry is strongly preferred.
3. English and Italian languages (professional knowledge).
4. Knowledge of the main chemical techniques (HPLC, TOC, UV...).
5. Excellent knowledge of Office Suite.