Scientist I

Target PR Range:

29-39/hr

• Depending on experience The candidate will collaborate cross-functionally to deliver high-quality nucleic acids and related data sets in a timely manner as well as ensure sufficient processing documentation using our sample management system (LIMS).

The successful candidate should be proficient in following established wet lab SOPs and protocols, execute role responsibilities autonomously, demonstrate technical precision and strong data interpretation skills, and possess an understanding of the core disciplines of biology, molecular genetics, and genomics.

Responsibilities:

The responsibilities of this job include:

• Perform sample processing activities adhering to established organizational and lab safety SOPs, policies, and procedures. Sample processing activities include but are not limited to routine and complex wet lab tasks to extract high-quality nucleic acids from source samples and generate nucleic acid QC data within agreed upon timelines.
• Drive curation and preliminary analysis and interpretation of nucleic acid QC data to accurately annotate and inform downstream workflows of extracted sample quality.
• Consistently follow documentation and data reporting policies and procedures
• Perform troubleshooting for routine wet lab tasks independently and report deviations
• Maintain active and open lines of communication within direct and matrixed teams
• Present data in scientific and/or technical meetings as applicable.
• Accurately document and record experimental setup, processing, and data quality control notes.
• Support downstream molecular workflows as needed with manager's approval and direction.
• Maintain wet lab instruments, such as those used for extraction and nucleic acid QC.
• Maintain documentation for experiments and instrumentation as outlined by laboratory standards.
• Assist as necessary with sample management duties including but not limited sample receipt, reconciliation and storage. Qualifications
• Experience required. BS degree in Genetics/genomic or related field or equivalent with 2+ years relevant experience, MS degree in Genetics/Genomics with 1+ years relevant experience.
• Theoretical and practical knowledge to carry out job function including but not limited to: o Experience with performing routine and or complex nucleic acid workflows from source material such as cells, tissues, blood, other biofluids.

o Experience with performing routine and/or complex nucleic acid quality control and analyzing/interpreting data for but not limited to fluorescence quantification, absorbance, and integrity analysis. o Proficiency in micropipetting techniques for accurate laboratory measurements. o Ability to strictly adhere to SOPs, documentation, and lab guidelines. o Strong computer skills, proficiency in Microsoft Office applications (Word, Excel, Powerpoint, etc) o Self-motivated and work independently in a fast-paced and fluid environment with high attention to detail. Preferred

• 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.
• Works well in a multidisciplinary team environment.
• Capacity to learn new methodologies/techniques quickly and drives innovation to improve workflows.
• Demonstrates effective and efficient communication.