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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical and manufacturing operations, including patient molecular testing and quality control. Proficient in laboratory information systems and regulatory compliance, with strong communication and organizational skills.
Highest-signal resume keywords
Bachelor's Of Science DegreeClinical Laboratory ExperienceImmunohematology KnowledgeMS Office ProficiencyTechnical Writing Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Molecular TestingSerologic TestingQuality Control MonitoringData SummarizationLaboratory Information System (LIS)SOP AdherenceCGMP ComplianceFeasibility StudiesEquipment CalibrationAssay Development
Soft Skills
Organizational SkillsTeam CollaborationWritten CommunicationVerbal CommunicationClient Interaction
Tools & Technologies
Microsoft Office SuiteMediaLabLaboratory EquipmentQuality Metric Data Tools
Certifications & Qualifications
CLS (ASCP) Certification
Industry Keywords
Clinical LaboratoryRegulatory GuidelinesQuality System Essentials (QSE)NAT TestingCGMP Environment
About the role
Key responsibilities & impact- Provide hands-on technical support for day-to-day clinical and manufacturing operations
- Perform patient molecular/serologic and manufacturing sample testing
- Perform and summarize data for review and reporting
- Monitor daily, weekly, and monthly quality control of equipment and systems
- Perform duties related to tests, instruments, and reagents; identify and escalate potential problems
- Maintain clean, organized laboratory and proper PPE/sample/material handling
- Log incoming materials and accession clinical samples in the Laboratory Information System (LIS)
- Transfer data accurately, generate electronic reports, document final results, and submit results for review
- Use LIS to sign off test completion and communicate results ready for review or release
- Report incorrect sample submissions and communicate written reports to clients
- Assist with training new employees and perform staff competency assessments
- Perform feasibility studies and assist in developing new assays
- Assist with strategic project testing and summarize data
- Participate in validation protocols and summarize validation data
- Perform annual equipment calibrations
- Use Microsoft tools to summarize quality metric data
- Support documentation of SOP deviations in MediaLab
- Enter deviations and CAPA submissions/updates in MediaLab
- Place online reagent and maintenance orders
- Maintain laboratory organization and appearance
Requirements
What you’ll need- Bachelor's of Science Degree in immunology, genetics, molecular biology, or related field
- 4 years of experience in a clinical or research laboratory environment
- Practical knowledge of immunohematology and molecular procedures including NAT testing
- Proficient in MS Office Suites
- Excellent organizational skills
- Ability to work on team projects
- Strong written and verbal communication skills
- Ability to communicate with all levels of staff and management
- Ability to interface with clients
- Proficient in technical writing for inclusion in regulated documents
- Must maintain technical competencies and annual continuing education credits
- Must be able to perform high-, mid-complexity, and simple routine tests
- Must adhere to SOPs, Quality System Essentials (QSE), cGMP, and regulatory guidelines
- Ability to lift and carry objects up to 50 lbs
- Ability to communicate complex information and understand instructions
- Ability to apply abstract principles to solve complex conceptual issues
- CLS (ASCP) or equivalent is a plus
- Experience in a cGMP environment is desirable
Benefits
Comp & perks- Regular Full-Time employment
- Equal employment opportunities consistent with applicable laws