QC Sr. Associate I (Software Developer Specialist) - Fixed Term
Core
Develop automated workflows and 'recipes' within the Biovia software system to bridge laboratory sciences and digital automation, ensuring data integrity and compliance in a regulated GMP environment.
Role type
Senior IC software developer specialist (Quality Control)
Builds
Automated laboratory workflows and system enhancements for pharmaceutical quality control operations
Domain
Pharmaceutical industry / Laboratory Informatics / GMP Compliance
Deliverable
production ML models | product features | infrastructure
Required skills
Biovia Software System expertise, BPMN fundamentals, cGMP regulations, Data Integrity concepts, validation principles, chromatography/spectrometry knowledge, independent project execution
Preferred skills
Life Sciences background (Biology, Biochemistry), analytical chemistry knowledge, experience with LIMS/ELN/LES systems
Technologies
Biovia Software System, LIMS, ELN/LES
Responsibilities
Design and modify complex laboratory workflows and automated recipes, partner with stakeholders to translate business requirements into system enhancements, detect and document software defects, design and enhance user interfaces and data reporting functionalities, prepare and maintain technical documentation and validation records, support integration of laboratory software and computerized analytical instruments
Seniority
Senior, hands-on IC