Staff Software Engineer
Rapid Micro Biosystems
Staff Software Engineer
Rapid Micro Biosystems
Automates microbial quality control testing workflows
Salary Range: 129000 to 172500 (Currency: USD) (Pay period: per-year-salary)
The Staff Software Engineer reports to the Development Manager within the R&D organization. This role is a key member of a highly collaborative Software Engineering team.
The ideal candidate is a self-motivated, full-stack software engineer who is capable of independently designing, developing, testing, and deploying high-quality software. As the secondary technical leader of the development team, this individual will serve as the primary backup to the Software Architect, contributing to technical design decisions, maintaining architectural consistency, and ensuring continuity of development efforts.
This position requires a strong background in modern software engineering practices, front-end and back-end development, cloud and on-premises deployments, CI/CD automation, and Agile development methodologies. Excellent communication skills and the ability to collaborate with multidisciplinary engineering, scientific and product management teams are essential.
Candidates should demonstrate strong experience in most of the following areas:
Automates microbial quality control testing workflows
Rapid Micro Biosystems provides automation solutions for microbial quality control in pharmaceutical manufacturing. It focuses on large and complex operations across biologics, vaccines, cell and gene therapies, and sterile injectables. The company’s Growth platform automates what were historically manual MQC testing workflows, using hardware and software systems to handle sampling, analysis, and data management so products can be released faster and with improved safety. What sets the company apart is its emphasis on end-to-end automation designed for large-scale, regulated biopharma environments, supported by ongoing maintenance and service contracts. The goal is to modernize MQC testing to speed product release, increase efficiency, and maintain high safety and quality in pharmaceutical manufacturing.
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