Quality Control Line Inspector

Quality Control Line Inspector x 2

Ref No.: CJCJ08912

Location: Tipperary, Cork, Cork city

Salary:

Experience required: 2 - 3 years

Job Type: Contract



Summary: Quality Control Line Inspector x 2 Tipperary



Description:

This is an excellent opportunity to join a leading medical device multinational as a Quality Line Inspector in the Tipperary area.

Position Description and Responsibilities

Perform in-line process audits to assure compliance with the manufacturing and quality procedures (visual inspections of randomly selected samples, verification of all the equipment, machinery, logbooks, process results and parameters according to specification at the MFG line)

Set up and use of equipment required by job function, ensuring conformance to specifications.

Perform and demonstrate basic understanding of sampling plans and statistical methodology.

Perform line clearance verification prior to start any phase and during the manufacturing process.

Perform batch record audits to verify that all documentation related to the Master Batch Record is present, completed and correctly issued, in accordance with applicable regulations, standard, and to company policies and procedures

Be responsible for assuring product segregation & proper identification according to its disposition and taking the lot to the appropriate quarantine location

Perform packaging audit prior to product shipment.

Perform manual and/or system quality related transactions, calculate and confirm the expiration dating, reconciliation, yield calculations

Interpretation of data, identify and solve potential issues using problem solving and decision-making techniques.

Responsible for evaluation, participation in investigation and closure of any open non-conformances prior to release the lot

Proficient in and ability to demonstrate basic computer skill set (e.g. use of Excel, Microsoft Word. etc.) and perform basic computer data entry functions and graphs / plots printing activities.

Interface with peers, supervision, engineering, Supply Chain, Production and management, professionally and respectfully in order to support Production schedules in a timely manner

Participate in the development of the Department KPIs

Support projects and/or assignments as required.

Works and has been certified as an online and offline auditor.

Read / interpret / understand written procedures

Maintains GMP compliance.

Ensure personal and peer adherence to all applicable FDA / ISO / State / Local / Company / Health-Safety / Environmental policies. Report infractions to supervision.

Accurate and legible data recording/calculations in logbooks, etc., on work completed and/or performed.

Perform functional testing as required by product

Perform configuration and visual inspections as required by procedure.



Other Skills

Leaving Certificate or equivalent is a minimum requirement, certification / diploma in life science related discipline desired.

Three to Five years of related experience and/or training; or equivalent combination of education and experience