Quality Assurance Inspector at GRIFOLS, S.A.

6th of October City, Giza, Egypt -

Full Time

Start Date

Immediate

Expiry Date

21 Mar, 26

Salary

0.0

Posted On

22 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Documentation, Compliance, Auditing, Inspection, Problem Solving, Communication, Organizational Skills, Time Management, Regulatory Knowledge, SOPs, Deviation Reporting, Team Collaboration, Health Sciences Knowledge, Integrity, Commitment to Quality

Industry

Pharmaceutical Manufacturing

Description

Quality Assurance (QA) Inspectors work with PLC operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor centers (DC), in-process production batches (Production Units - PUs), and the final Plasma Lot shipment for distribution and sales at the Grifols Plasma Logistics Center (GPLC). QA Inspectors identifies and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers. Environment Internal and external interactions i.e.: with other departments/divisions, international scope, providers, customers) Internal: PLC Operations, Look Back Specialist, Manufacturing Facility. External: Auditors. Key responsibility: Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor. Monitors the quality of the production operation by constantly auditing the production process to ensure compliance with customer specifications and GPLC standard operating procedures. Generates and documents non-conformance of plasma units rejected from plasma shipments, in process batches or final plasma Lots. Approves in-process plasma batches (PU's) and final plasma lot shipments by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor. Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution. Investigates and reports in-process/final plasma lot and processes that do not meet quality specifications and document in a deviation report. Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at Plasma Warehouse level. Documents approval activities in the organizations computer system (Plasma Logistic System- PLS) to maintain accurate records. Academic experience required: Bachelor's degree in health-related Sciences. Knowledge in quality Management. Strong integrity and commitment to quality and compliance. Professional Experience Required: Typically requires a minimum of 2 years of related experience. Preferred Pharma background. Computing Skills: Proficiency with computers. Personal Skills: Organized and able to manage time effectively. Ability to work within a highly regulated, labor intensive environment. Ability to understand, explain, follow, and enforce SOPs and protocols. Ability to plan, communicate and execute activities for the improvement of overall operations. Languages: Written and spoken English and Arabic.

Responsibilities

QA Inspectors approve incoming plasma shipment documentation and raw materials, monitor production quality, and document non-conformance. They also inspect final outgoing plasma lot shipments and participate in writing or revising quality-related policies.