Control Quality Specialist

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. 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.

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.

Enters components, semi-finished and finished products into the management system and ensures their quality release.

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;

Manages the calibration of measuring instruments used in production also with the collaboration of qualified external laboratories;

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 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

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.

Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate.