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For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently…
Leads product lifecycle management projects in biotech/medtech/pharma, overseeing planning, execution, and stakeholder communication across technology transfer and regulatory domains.
The Benchling Solutions Consultant provides implementation and managed service support for the Benchling platform, including system configuration, data migration, and training for biotech and pharmaceutical clients. The role involves managing Benchling environments, creating workflows, and developing dashboards to support scientific research operations.
Scientific Data Engineer Consultant designing and maintaining AWS-based data pipelines (Glue, Aurora, Redshift) using Python to ingest and transform scientific instrument data for pharmaceutical/biotech clients in CRO/CDMO environments.
Designs electronic case report forms (eCRFs) for clinical trials using Oracle InForm/Central Designer or Veeva CDMS/Studio, ensuring compliance with standards and timelines.
Directs a biotech client’s GMP readiness plan, building QMS, 21 CFR Part 11 compliance, and design controls for instruments, software, and consumables to accelerate product launch.
Oversee biotech/pharma facility projects, coordinating contractors and stakeholders to ensure commissioning, qualification, and operational readiness on time.
Conducts GCP and GVP audits for clinical trials and pharmacovigilance systems in Japan, ensuring compliance with Japanese and international regulations.
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