QA Associate

23 November 2021
SalaryUp to £0.00 per annum
DisciplineQuality Assurance/Safety

For our client, a company in Pharmaceutical, we are looking for a QA Associate based in Breda.

Knowledge of basic principles, methods and practices of scientific/technical field, typically obtained through formal study
General knowledge of procedures and activities within own work area
Ability to relate day-to-day work to business priorities
General understanding of industry practice and standards

Problem Solving
Applies broad-based research, information gathering and analytical skills to factual information
Selects appropriate alternatives from defined options
Collects required documentation/raw data; verifies conformance of documents
Assesses accuracy of detailed information
Tracks, maintains and produces regular work products
Ability to identify roadblocks to task completion and effectively brings them to line managers for resolution

Works under general direction, seeks assistance as needed
Completes work in accordance with established procedures and practices within field of scientific/technical knowledge
Establishes approaches for completing assignments
Work requires consistent exercise of discretion and independent judgment

Contributes to the work group/team through quality and accuracy of the output
Builds productive internal/external relationships

Ensure IDP/ FDP batches are ready for release by the QP and all procedural requirements for release have been met.
Execute sampling, inspection, review and release of incoming materials.
Execute sampling and/or inspection of IDP / FDP / NAMP.
Initiate and own class 1 deviations related to IQA and WH activities.
Establish effective working relationships with WH, QA management and the QP.

Position Specific Tasks
Sampling and Inspection of IDP and review completed IDP batch records ensuring all procedural requirements are met
QC Lab data authorization in LIMS
Test sample planning and sample management (coordination between AML, ADL, ABR and Test Labs)
Sampling and Inspection of FDP and review completed FDP batch records ensuring all procedural requirements are met
Sampling, inspection, review and release of printed and non-printed packaging components
Review temperature data of shipments received at ABR
Sampling and Inspection of drug products as needed
Preparing samples for shipment to contract laboratories
Provide QA oversight for:
Regulatory labeling in the WH
Issues upon receipt of components / IDP / FDP / NAMP
Destruction Authorizations
Cancelled Ship Confirmed Orders
Initiate and own class 1 deviations related to IQA and WH activities

Chaima Aboulhadi
T: 0031 618674361
When interested please react through the application process with your English resume.

About Kelly Services
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