Principal Scientist, Bioanalytical & Molecular Assays
GBR - OX - Clinical - Harwell, United Kingdom
GBP 80K-93K (estimate) Senior-level Full Time
Tasks
- Author protocols and acceptance criteria
- Author validation plans and reports
- Deploy molecular assays
- Design molecular assays
- Develop bioinformatics pipelines
- Develop molecular assays
- Ensure data integrity
- Execute method development
- Execute qualification and validation
- Lead CAPA activities
- Lead deviation investigations
- Manage quality assurance
- Manage quality control
- Mentor colleagues
- Optimize molecular assays
- Oversee clinical sample testing
- Own assay lifecycle activities
- Perform RT qPCR assay development
- Perform droplet digital PCR assay development
- Perform next generation sequencing assay development
- Perform technology transfer
- Prepare for inspections and audits
- Translate molecular data into recommendations
- Validate molecular assays
Perks/Benefits
- Adoption benefits
- Discretionary year end shutdown
- Fertility benefits
- Fitness resources
- Global recharge days
- Health insurance
- Mental health support
- Mindfulness support
- Paid time off
- Sabbatical
- Savings and investments
- Surrogacy support
- Voluntary benefits
- Volunteer days
Skills/Tech-stack
Amplicon sequencing | Bioanalyzer | Bioinformatics | CAPA | DPCR | Data Governance | Data handling | Digital Data | Digital data handling | ELN | GCLP | GLP | GxP | GxP Compliance | Hybrid capture | ICH | ICH inspection readiness | Inspection Readiness | LIMS | Library preparation | NGS | Nucleic acid extraction | Poly A RNA extraction | Quality Assurance | Quality Control | RNA extraction | RT-qPCR | TapeStation
Education
Roles
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