Teams at DifGen Pharmaceuticals

Support new research projects within the group by performing experimental work, data collection and documentation, and collaborating with team members to advance project objectives.

Senior QA responsible for reviewing and submitting exhibit batch manufacturing and packing records, process validation and hold-time protocols/reports, executed media fill records, equipment qualification documents, and QMS documents (change control, deviations, CAPAs) for regulatory submissions.

Support execution of commercial launches, scale-up and validation batches at internal and CMO manufacturing sites. Prepare and review BMRs and validation protocols/reports, coordinate cross-functional knowledge transfer, participate in investigations and deviation handling, assist equipment selection, support regulatory submissions and audits, and maintain GMP-compliant documentation and reporting.