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QC Sampling Technician
Job in
03013, Ferentino, Lazio, Italy
Listed on 2026-08-11
Listing for:
Thermo Fisher Scientific
Full Time
position Listed on 2026-08-11
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers
Job Description & How to Apply Below
This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
Work Schedule
Flex Shifts 40 hrs/wk Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Job Description
Job Summary
Performs sampling activities for pharmaceutical raw materials, packaging components, intermedi, and finished products in compliance with GMP, SOPs, and safety guidelines. Ensures samples are representative, properly handled, documented, and delivered to the QC laboratory for analysis.
Key Responsibilities
Performs sampling of raw materials, packaging materials, intermedi, and finished products according to approved procedures and sampling plans.
Ensures correct identification, labeling, and traceability of collected samples.
Operates within classified environments (e.g., clean rooms, warehouses) following GMP requirements.
Performs cleaning and verification of sampling tools and equipment before and after use.
Documents all sampling activities accurately in logbooks and electronic systems (e.g., LIMS).
Recognizes and reports deviations, discrepancies, or non-conformities during sampling activities.
Supports investigations (e.g., deviations, OOS) when required.
Coordinates with QC laboratory and warehouse personnel for sample management and logistics.
Ensures compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines at all times.
Maintains sampling areas in a clean and organized state.
Education
Diploma or degree in a scientific or technical field is recommended (e.g., Chemistry, Biology, Biotechnology, or similar).
Experience
0–2 years of experience in a GMP environment (QC, production, or warehouse preferred).
Previous experience in sampling activities is considered a plus.
Knowledge, Skills, Abilities
Basic knowledge of GMP requirements and data integrity principles.
Familiarity with documentation practices (paper-based and/or electronic systems such as LIMS).
Proactivity and attention to detail.
Flexibility and ability to work in a dynamic environment.
Problem-solving attitude.
Good organizational and communication skills.
Ability to work both independently and as part of a team.
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