We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs.
We have leveraged our expertise and capabilities both to commercialize three vaccines, including the world’s first and only chikungunya vaccine, and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease and Zika.
With operations in Austria, Canada, France, Sweden, the United Kingdom, and the U.S., we are committed to making a positive impact on global public health.
Together, we are a global Company which is open to people of all backgrounds. Our diverse and inclusive workforce makes Valneva a great place to work.
Our QC Mirco team have a fantastic new opporutnity to join the team here in Livingston, To undertake microbiological tasks and analysis for the release and monitoring of facilities, raw materials, intermediate and final product samples according to defined procedures and protocols, in accordance with regulatory requirements
Requirements
Responsibilities include:
Perform Microbiological procedures including Total Viable Counts, Growth Promotion, Gram Stain, Microbial Growth Check by Incubation and Endotoxin for testing of raw materials, intermediate products and final product samples, according to defined SOPs and protocols
Perform In Operation & At Rest Environmental monitoring of Cleanrooms & Support areas as required, to support manufacturing processes and Facility Contamination Control (FCC)
Comply with GMP guidelines and regulatory body requirements
Full compliance with HSE requirements
Write QMS documentation, e.g. SOPs, Deviations, Change Controls, CAPA
Maintain, databases, logs and support the generation of QC trend data
Be responsible for QC Laboratories being clean, tidy and well-organised and in a state of continuous inspection readiness
Ability to work in a supportive and collaborative team setting and work individually as when required.
Shift work and out of hours work as required
Your Experience ideally includes the following:
Degree in Microbiology or related subject or relevant experience
Demonstrable experience working in a GMP environment
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