Quality Control Specialist

H.B. Fuller; Viareggio; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A global adhesives company is seeking a Quality Control Specialist in Viareggio. This role involves managing and recording quality controls on products and ensuring compliance with quality management systems. Candidates should have a degree in chemistry and at least 3 years of experience in the medical device field, with strong knowledge of relevant standards and procedures.

Competenze

• 3 years of experience in quality control within the medical device field.
• Good knowledge of quality management systems and procedures.

Mansioni

• Manage and record quality controls on products.
• Implement sampling plans and manage product quality.
• Perform inspections at suppliers' premises.

Conoscenze

Knowledge of UNI CEI EN ISO 13485 standard

Experience in the medical device field

Knowledge of statistical processes

Knowledge of quality control procedures

English language proficiency

Formazione

Degree in chemistry or equivalent technical and scientific subjects

Descrizione del lavoro

As the largest pureplay adhesives company in the world, H.B. Fuller’s (NYSE: FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day. Founded in 1887, with 2024 revenue of $3.6 billion, our mission to Connect What Matters is brought to life by more than 7,500 global team members who collaborate with customers across more than 30 market segments in over 140 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets. Learn more at www.hbfuller.com.

Position Overview

The Quality Control Specialist manages and records incoming and outgoing quality controls on the finished product. Assists QA in setting up, issuing, storing, distributing and maintaining QMS documents and Technical Files.

Primary Responsibilities

• Implements the sampling plans issued by QA, manages and records all acceptance and final quality control activities (also in cooperation with external laboratories) in accordance with specific procedures and company control plans.
• Collects the DHR documents and completes them for the parts under its remit
• Enters components, semi-finished and finished products into the management system and ensures their quality release.
• Checks the correct use of the control areas in the warehouse;
• Checks that the recorded data on the storage conditions of the products in the warehouse are compliant;
• Provides QA with data on any non-conformities found upon acceptance, in-process and on finished products for the development of process performance indicators as well as for the review of the sampling plans used;
• Manages and records the maintenance work carried out on the instrumentation in use at the in-house laboratory;
• Maintains contact with external laboratories in charge of carrying out quality control tests;
• Opens and manages, with the cooperation of QA, any product/process non-conformities;
• Together with QA, carries out inspections at the suppliers' premises in order to verify the adequacy of their QMS;
• Manages the calibration of measuring instruments used in production also with the collaboration of qualified external laboratories;
• Issues equipment master sheets and scheduled routine maintenance plans and transmits them to OM;

Minimum Requirements

• Degree in chemistry or equivalent technical and scientific subjects.
• Experience of 3 years in the medical device field
• Good knowledge of the general requirements of the UNI CEI EN ISO 13485 standard, the general QMS, the specific rules and regulations of the medical devices sector as well as of the company's quality control procedures.
• Good knowledge of sampling procedures and statistical processing;
• Good knowledge of the type and technical, qualitative and functional characteristics of in-house manufactured medical devices.
• Good knowledge of internal control procedures, DMRs, the company's traceability system and the recording of production and control phases of products manufactured in-house and at external suppliers;
• Good knowledge of the English language

H.B. Fuller is an Equal Employment Opportunity employer and proud to have created a collaborative culture where employees around the world are seen, heard, and respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, or marital status or status as a protected veteran, or any other legally protected classification.

H.B. Fuller does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with H.B. Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate. Without a signed service agreement, H.B. Fuller shall not be obligated for payment of any fee or compensation.