
Quality Control Officer, Medical Devices
RONTIS HELLAS
Πλήρης απασχόληση
Λάρισα
We are seekingto employ a highly skilled and experienced Quality Control (QC) Officer, responsible for performingtests, measurements and inspections, for recording and analyzing data and for collaboratingclosely with other departments for addressing quality issues and implementingimprovements. The role is located at company’s manufacturing site in Larissa,Greece.
Key responsibilities - main job duties include the following:
- Supports quality control testing in laboratory,production and facility’s areas (material and products sampling, qualitycontrol, calibration activities etc.)
- Assists in investigating product complaints andassists in taking appropriate action
- Assists in investigating quality issues duringproduction related to the produced product as far as the quality and theperformance
- Assists in carrying out QC studies related with theproducts produced on site and QC studies concerning the infrastructure (e.g. sterilization validation studies etc.)
- Supports microbiological testing and sterilizationcontrol processes
- Supports internal & external audits needs, assists in CAPA plan establishment, root-causeanalysis, investigation and follow-up.
- Collaborateswith medical device production team to ensure quality is integrated into all productionprocesses and phases
- Participates inthe preparation and review of SOPs, Procedures, work instructions and relevantdocuments
- Participates in change control forms issuance andfollow up in cooperation with QC Manager, Medical Devices
- Interacts closely with Production, R&D, QA/RA andCompliance departments
Requirements:
- University Level Degree in chemistry, microbiology, biologyor a related field
- Prior experience in the wider laboratory field (microbiologycontrol, HPLC, GC etc.); three (3) years of full-time laboratoryexperience will be considered a plus
- Prior experience in the wider pharmaceutical ormedical device field will be considered a plus
- Solid knowledge and understanding of ISO standards,GMP, GLP
- Capable of prioritizing and handling multiple tasks,projects, and deadlines
- Ability to research, digest, analyze and present dataclearly and concisely
- Responsible, pays attention to detail, demonstratesspeed and accuracy
- Positive personality, energetic
- Multi-tasking, demonstrating flexibility
- Excellent oral & written communication skills inboth Greek & English language
- Computer literacy
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