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Immunoassay Method Development (Associate Principal Scientist)

Aplica ya
Mapa de ubicación: Durham, North Carolina, United States Full time R1306193

Descripción del trabajo

Job Overview
The Associate Principal Scientist for Assay Development applies advanced comprehensive knowledge of assigned area to provide technical leadership on complex assay/method development.  Responsible for collaborating with clients to provide solutions for client needs.  


RESPONSIBILITIES 
• Responsible for performing complex assay/method development.
• Responsible for execution of assay/method development experiments.
• Establishes the assay/method procedure to ensure effective operational execution.
• Evalutes, recommends, and implements new technology and instrumentation.
• Leads complex technical projects and guide the work of junior staff.
• Works proactively across functions to identify opportunities for innovation and troubleshoot challenges to ensure effective delivery to the customer and deployment of the method.
• Applies knowledge to leverage opportunities to deploy method across multiple studies.
• Drives opportunities for process and operational efficiencies.
• Leads training initiatives to support continuous learning and development of lab staff.
• Maintains scientific awareness of overall developments in area of expertise based on current literature and application of new technologies and experimental techniques.
• Utilizes scientific awareness to bring innovative ideas for assay and method development.
• Contributes to scientific literature and conferences, internal reports, documents and communications including the writing and/or creation of abstracts, peer-reviewed journal articles, poster presentations, and marketing materials.
• Provides technical support for the maintenance and operational standards of laboratory equipment.
• Provides and disseminate meaningful data analysis and interpretation of experimental findings in acceptable laboratory formats.
• Provides project updates/reports of deliverables to project manager, as requested.
• Maintains laboratory notebooks under applicable regulatory standards and good documentation practices.
• Contributes to quality, safety and Six Sigma initiatives.
• May review laboratory notebooks.
• May present findings to a wide variety of audiences internal and external to Q2 Solutions.
• Follows all appropriate lab and company procedures and policies. Performs work in accordance with applicable regulatory requirements.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• Bachelor's Degree Bachelor's degree in relevant scientific discipline required
• 7 years of related experience in method or assay development or specific methodology area.

REQUIRED KNOWLEDGE,SKILLS,AND ABILITIES
• Advanced knowledge of assay/method development and scientific principles, theories, concepts, and state of the art instrumentation.
• Developing understanding of the relevant industry and applying that knowledge to the improvement of their business unit.
• Understands the phase of development relevant to the assigned assay and interactions/implications of assay development across cross functional areas.
• Ability to process and apply complex information from various topics.
• Strong troubleshooting capabilities.
• Good computer skills including proficiency with Microsoft Excel, PowerPoint and Word.
• Advanced skills in utilizing software solutions that support experimental data analysis.
• Good problem solving, troubleshooting, and analytical skills.
• Effective organizational, interpersonal, and time management skills.
• Effective communication skills and presentation skills.
• Ability to effectively coordinate and execute multiple tasks or projects simultaneously.
• Ability to effectively write scientific and technical documents.
• Ability to work closely with multiple departments and to contribute in multi-disciplinary discussions.
• Ability to establish and maintain effective working relationships with co-workers, managers, and clients.
• Ability to maintain a high degree of independence and motivation needed to complete assigned tasks and projects.
• Basic knowledge of requirements under relevant regulatory standards for assigned work area.
• Demonstrated “everyday leadership” skills.

Q² Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. https://www.q2labsolutions.com/careers

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/q2-solutions-eoe

As the COVID-19 virus continues to evolve, Q² Solutions' ability to operate and provide certain services to customers and partners necessitates Q² Solutions and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/q2-solutions-covid-19-vaccine-status

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