Manufacturing Technician (Scientist)

Social network you want to login / join with :

Manufacturing Technician (Scientist), Livingston

col-narrow-left

Client : Location :

Livingston, United Kingdom

Job Category : Other

EU work permit required :

col-narrow-right

Job Reference : 81e6ac0229cb

Job Views : Posted :

22.06.2025

Expiry Date : 06.08.2025

col-wide

Job Description :

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 manufacturing team is recruiting for a Manufacturing Scientist to join our Vaccine manufacturing processes.

The purpose of this role is to execute defined manufacturing support steps for the production of Vaccine Candidates according to set procedures and protocols, adhering to cGMP work practices and Quality standards. The role involves acting as the SME, understanding the process, sharing knowledge, and improving the process.

Requirements

• Execute production steps defined by SOPs, production records, and protocols for vaccine manufacture.
• Conduct activities in a careful, safe manner, complying with HSE requirements.
• Raise safety concerns via EMS reporting system and flag at level 1 VAC.
• Ensure personal and colleagues' safety at all times.
• Apply best cGMP work practices and techniques.
• Provide technical support for manufacturing, including deviation management and validation activities.
• Report activities promptly according to documentation standards.
• Immediately escalate deviations related to materials, facilities, processes, or procedures.
• Complete documentation following ALCOA+ principles.
• Contribute to safety assessments like COSHH.
• Maintain a clean, tidy, and organized workspace.
• Work shifts and out-of-hours as required.
• Participate actively in process improvements.
• Undertake additional duties as requested by the line manager.
• Identify and escalate areas for continuous improvement.
• Contribute to a positive, collaborative team environment.

J-18808-Ljbffr