Scientist ; Genetics​/Genomics

Overview

Scientist 1(Genetics/Genomics) $38 - $41/hr medical benefits available at a cost

6 month initial contract

Onsite – Lake County, IL

Orion Group and a market leading pharmaceutical company are teaming up for an exciting contract opportunity in North Chicago, IL! Our client is seeking an experienced and highly organized Sample Management and Processing Scientist (I) to support impactful reverse translation focused projects.

Apply today and take the first step towards your next career opportunity!

The Genomics Research Center (GRC) is part of the Quantitative Medicine and Genomics (QM&G) functional area that promotes data-driven innovation in drug discovery by integrating diverse quantitative data and leveraging advanced computational models. The GRC’s goal is to develop world class genetics and genomics research focused on finding the right therapeutic targets and helping scientists better understand not only human disease biology but also the behavior and response to our drugs in clinical trials across all therapeutic areas.

Join our innovative Genomic Technologies (GTECH) lab team, where we are at the forefront of genomic research and discovery. Our team is dedicated to advancing science through cutting-edge technologies and collaborative efforts.

• Responsibilities will center on supporting gDNA isolation from clinical samples across multiple therapeutic areas.
• Scientist (I) will execute manual and automated workflows for high-quality nucleic acid extraction, perform rigorous quality control assessments on isolated nucleic materials, maintain detailed and accurate documentation in LIMS, and interpret and report QC data.
• In addition, effective cross-functional communication with researchers is essential to ensure the integrity and utility of isolated gDNA for downstream analyses.
• Adhere to department generated and company standard operating procedures for communication, lab operations, project reporting, and lab safety.
• Attain operational proficiency for required daily functions within training schedules.
• Perform troubleshooting for wet lab tasks independently and with collaboration.
• Maintain clear and accurate documentation of all processes.
• Formally and informally communicate project progress, completion, and data by delivering reports through collaborative meetings, and verbal or written presentations.
• Timely recording and documentation of wet lab processes and progress in applicable LIMS and project management applications in accordance with policies and procedures.
• Support the development and testing of LIMS workflows.
• Maintain instrumentation as outlined by laboratory standards and manuals.

• Experience required. BS degree in Genetics/genomic or related field or equivalent with 4+ years relevant experience, MS degree in Genetics/Genomics with 2+ years relevant experience.
• Theoretical and practical knowledge to carry out job function including but not limited to:
• Experience with performing routine and or complex nucleic acid workflows from source material such as cells, tissues, blood, other biofluids.
• Experience with performing routine and/or complex nucleic acid quality control and analyzing/interpreting data including but not limited to fluorescence quantification, absorbance, and integrity analysis.
• Experience with sample processing from source materials to nucleic acids within a laboratory management system.
• Proficiency in micropipetting and wet lab automation for multiple genomic laboratory techniques.
• Ability to strictly adhere to SOPs and lab guidelines and thoroughly report deviations in a timely manner.
• Strong computer skills, especially in Microsoft Office Suite.
• Self-directed to deliver timely results both independently and collaboratively in a fast-paced and fluid environment with high attention to detail.
• Strategic project planning and critical thinking to resolve routine and complex problems.

• Experience with low and high throughput sample tracking and data management (LIMS).
• Experience with performing and maintaining workflows on automation platforms.
• Experience in a CLIA certified laboratory or other regulated laboratory environments.
• Experience in clinical writing and editing documents/manuals.

Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion.

In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.