Senior Associate Scientist, IVD Test Dev

Cleveland Diagnostics; Cleveland (OH); Vor Ort; USD 80.000 - 110.000; Vollzeit

Zusammenfassung

Cleveland Diagnostics Inc. in Cleveland, OH is seeking a Senior Associate Scientist-IVD Test Development to support regulated assay development and validation, including PMA, 510(k), and IVDR submissions.

The role requires hands-on lab work, data analysis, and documentation in a GDP/QMS-compliant environment, with emphasis on planning experiments, troubleshooting, and collaborating across teams.

Qualifikationen

• Bachelor's degree in biology, Biochemistry, Molecular Biology, or a related field with2-4 years of relevant experience.
• Master's degree with1-2years of experience
• Industry experiencepreferable

Aufgaben

• In collaboration with a supervisor, design and plan laboratory experiments with clearly defined objectives and success criteria.
• Independently execute laboratory experiments supporting assay development, optimization, verification, and validation in accordance with approved protocols and design control requirements.
• Provide technical input toward refinement of new diagnostic assays and improvements to existing assay workflows.
• Independently apply basic to intermediate statistical analyses to study results and ensure data accuracy and integrity.
• Prepare data summaries, figures, tables, and preliminary interpretations for internal technical review.
• Maintain complete, accurate, and GDP/QMS-compliant experimental records and documentation.

Kenntnisse

Pipetting and reagent preparation

Data analysis

Laboratory troubleshooting

Regulatory familiarity (FDA/ISO)

MS Office proficiency

Automated immunochemistry analyzers

Documentation and records

Ausbildung

Bachelor's degree in biology, Biochemistry, Molecular Biology, or a related field

Master's degree

Tools

Microsoft Office

Jobbeschreibung

Senior Associate Scientist, IVD Test Dev

Cleveland Diagnostics Inc. Cleveland, Ohio, United States

About this position

We are seeking a Senior Associate Scientist-IVD Test Development to support in-vitro diagnostic assay development and validation activities within a regulated environment operating under design control. The successful candidate will execute laboratory experiments and contribute to assay optimization, verification, and validation studies in support of regulatory submissions including PMA, 510(k), and IVDR.

The Senior Associate Scientist will support in-vitro diagnostic assay development and validation activities within a regulated environment. This role will execute laboratory experiments and contribute to assay optimization, verification, and validation studies supporting regulated diagnostic products requiring PMA, 510(k), and IVDR submissions, as well as laboratory-developed tests (LDTs) which are validated for internal clinical laboratory use. The position requires strong hands-on technical skills, attention to detail, and the ability to follow established protocols while contributing to experimental planning and troubleshooting under the guidance of a supervisor. The Senior Associate Scientist will perform routine and non-routine laboratory procedures, analyze and summarize data, maintain accurate documentation in accordance with quality system requirements, and assist in preparing technical reports and study documentation. In addition to laboratory execution, this position will support lab organization, equipment maintenance, reagent preparation, and continuous improvement initiatives to ensure efficient study execution. The role involves handling human biological specimens, including blood, plasma, urine, and other bodily fluids, in compliance with all safety regulations and company policies.

Essential Duties and Responsibilities

• In collaboration with a supervisor, design and plan laboratory experiments with clearly defined objectives and success criteria.
• Independently execute laboratory experiments supporting assay development, optimization, verification, and validation in accordance with approved protocols and design control requirements.
• Provide technical input toward refinement of new diagnostic assays and improvements to existing assay workflows.
• Independently apply basic to intermediate statistical analyses to study results and ensure data accuracy and integrity.
• Prepare data summaries, figures, tables, and preliminary interpretations for internal technical review.
• Maintain complete, accurate, and GDP/QMS-compliant experimental records and documentation.
• Perform routine troubleshooting of assays, instrumentation, and laboratory workflows; elevate complex issues appropriately.
• Prepare reagents, solutions, and study materials while ensuring traceability and proper documentation.
• Demonstrate accountability for assigned workstreams, meeting study timelines, documentation standards, and data quality expectations.
• Coordinate with vendors and internal teams to procure laboratory supplies and maintain operational readiness.
• Actively participate in technical discussions, team meetings, and cross-functional reviews.
• Ensure compliance with all safety policies, biosafety procedures, laboratory standards, and company requirements.
• Other duties as assigned

Qualifications/Requirements

• Bachelor's degree in biology, Biochemistry, Molecular Biology, or a related field with2-4 years of relevant experience.
• Master's degree with1-2years of experience
• Industry experiencepreferable

Technical Skills

• Hands-on experience with standard laboratory techniques such as pipetting, reagent preparation, and handling. (Experience with automated immunochemistry analyzers preferred).
• Ability to follow standard protocols and troubleshoot routine lab tasks
• Experience with data analysis and documentation best practices
• Familiarity working in an FDA or ISO-regulated environment is a plus
• Proficient with computer skills and with Microsoft Office applications

Physical Requirements/Working Conditions/Equipment Used

• Fine motor skills and manual dexterity to handle specimens and lab equipment required to process specimens, troubleshoot and repair instrumentation.
• Visual acuity to examine specimens and reagents
• Offices reachable by elevator but should be able to climb stairs if needed
• Light lifting may be required (up to 25 pounds)
• May be required to stand for long periods of time
• Ability to operate a computer and other technology related lab equipment through course of day
• Ability to work in an environment with exposure to hazardous chemicals and biohazards
• Ability to comply with all appropriate job PPE requirements
• General office and HVAC noise and fluorescent lighting

Other Requirements

• Full-time on-site position; this is not a remote position
• May require infrequent travel
• Requires Hepatitis B vaccination or appropriate waiver (working with blood-based samples)
• This position is classified as exempt and may require work in excess of 8 hours per day and/or 40 hours per week as business needs dictate
• Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards.