QA Specialist II

15 November 2021
Salary€4000 - €4500 per month + Negotiable depending on experience
LocationHoofddorp
Temporary
DisciplineHealthcareLife Science Careers
ReferenceBBBH494408_1636970841


Our client, who is an international pharmaceutical, is looking for QA Specialist II in Hoofddorp.

All applicants MUST have full legal authorization to work in the EU region independently and be fluent in both spoken and written English language.

Responsibilities
* Performs a wide variety of QA activities to ensure compliance with applicable regulatory requirements and Kite procedures.
* Maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs),
* Reviews manufacturing, environmental monitoring and quality control data for in process and finished products.
* Compile final product binders for the QP release and perform QA disposition
* Contribute to the Quality on the floor processes, including GEMBA walks and maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs), and Kite procedures.
* Conducts or acts as a coordinator of investigations and corrective and preventive action (CAPA) recommendations related to manufactured products and performs QA review and approval of complex deviations and CAPA and contributes to cross functional investigations.
* Identifies deviations from approved procedures and processes, evaluates impact assessments and develops solutions for complex problems.
* Contributes to QA projects.
* Works on mid complex, non-routine projects/assignments where analysis of situation or data requires a review of identifiable factors.

Requirements
We are seeking a highly motivated individual which likes to join the international QA Operations Disposition team. The ideal candidate for this position is flexible, has great communication skills and feels comfortable challenging existing processes. This person has a critical eye and enjoys review work and daily interaction with QPs.

Education and experience:
* 4+ years of experience in a GMP environment and a BSc degree OR
* 2+ years of experience in a GMP environment related and MS (Master in Science).

Preferred:
* Prior experience in pharmaceutical industry or similar bio industry is preferred.

What do we offer
· Temporary agency contract via Kelly for 40 hours duration 6 months with possible extension
· Start date: 1 January 2022

· Salary indication depending on experience: max. € 4500,- gross per month based on 40 hours

Enquiries
Please do contact Marcella Henryati, Recruitment Consultant
M: 06-58811958
When interested please apply with your English resume on our website: www.kellyservices.nl

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Regarding this role, Kelly Services acts as the official temporary employment agency. When you decide to apply to this role your personal information will be processed in accordance with Kelly's Privacy Statement

In keeping with the AWGB (Algemene Wet Gelijke Behandeling) Kelly Services welcomes applications from any and all eligible candidates regardless of ethnicity, gender, disability, religion, sexual orientation or age.