Technical Specialist
SRG is seeking a highly motivated Technical Specialist to join a Manufacturing Process Development team in Loughborough. In this role, you will play a key role in ensuring the smooth implementation of lean manufacturing principles, supporting technical investigations, and driving continuous improvement within GMP Operations.
About You:
• A minimum of 2-3 years' experience in a similar role within a regulated environment (e.g., Pharmaceuticals)
• Strong understanding of lean manufacturing principles (e.g., 5S, Kanban)
• Excellent technical writing and communication skills
• Bachelor's degree (or equivalent) in a related Scientific/Technical discipline or significant relevant experience working within the Pharmaceutical Manufacturing industry in an Operations Environment
• Experience in the technical transfer, scale- up, and process validation of equipment and processes.
What You'll Do:
• Implement and maintain 5S housekeeping standards within the GMP Operations Facility
• Collaborate on the creation and improvement of Standard Operating Procedures and Work Instructions
• Develop and deliver technical training programs for complex equipment and processes
• Support the transfer of new technologies and processes to Development and Commercial Production
• Provide technical expertise to troubleshoot process challenges and investigate quality concerns
• Manage the qualification of process equipment modifications and support project teams in selecting optimal solutions
• Offer technical support for the validation and transfer of new commercial manufacturing processes
• Proactively contribute to the improvement of the Pharmaceutical Quality System by identifying and addressing inefficiencies
• Represent Manufacturing Process Development in cross-functional teams and effectively communicate with various departments
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
About You:
• A minimum of 2-3 years' experience in a similar role within a regulated environment (e.g., Pharmaceuticals)
• Strong understanding of lean manufacturing principles (e.g., 5S, Kanban)
• Excellent technical writing and communication skills
• Bachelor's degree (or equivalent) in a related Scientific/Technical discipline or significant relevant experience working within the Pharmaceutical Manufacturing industry in an Operations Environment
• Experience in the technical transfer, scale- up, and process validation of equipment and processes.
What You'll Do:
• Implement and maintain 5S housekeeping standards within the GMP Operations Facility
• Collaborate on the creation and improvement of Standard Operating Procedures and Work Instructions
• Develop and deliver technical training programs for complex equipment and processes
• Support the transfer of new technologies and processes to Development and Commercial Production
• Provide technical expertise to troubleshoot process challenges and investigate quality concerns
• Manage the qualification of process equipment modifications and support project teams in selecting optimal solutions
• Offer technical support for the validation and transfer of new commercial manufacturing processes
• Proactively contribute to the improvement of the Pharmaceutical Quality System by identifying and addressing inefficiencies
• Represent Manufacturing Process Development in cross-functional teams and effectively communicate with various departments
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
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