Associate Scientist 2 - Assay R&D #4992

Responsibilities

• Perform a range of established laboratory experiments using professional methods in molecular biology, including RNA isolation, genomic DNA isolation, cDNA preparation, cloning, fermentation, protein expression, and purification with increasing independence and accuracy.
• Prepare, process, and analyze samples, reagents, buffers, and media for experimental workflows while applying professional judgment to ensure precision, proper documentation, and procedural compliance.
• Collect, interpret, and document experimental data in laboratory notebooks or electronic systems using professional data management practices that support reproducibility and scientific integrity.
• Operate, maintain, and perform routine troubleshooting on laboratory equipment, identifying issues that require escalation and ensuring continuous readiness of instruments used in scientific work.
• Assist in refining laboratory protocols or methods by providing professional observations on workflow efficiency, data quality, and opportunities for procedural improvement.
• Contribute to the preparation of technical reports, data summaries, protocol drafts, and quantitative analyses to support scientific communication and project decision-making.
• Ensure adherence to safety, regulatory, and quality standards in the handling of chemical and biological materials, demonstrating accountability for maintaining a professional laboratory environment.
• Support laboratory operations through inventory oversight, organization of materials, coordination of supply needs, and contributions to continuous process improvements.
• Provide informal guidance and technical support to junior laboratory staff by sharing professional knowledge, reinforcing documentation standards, and modeling effective laboratory practices.

Required Qualifications

• Bachelor's degree in Biology, Chemistry, Biochemistry, or related scientific discipline with 2-5 years of relevant experience; OR Master's degree in a related field with 0-2 years of relevant experience.
• Demonstrated knowledge of applicable regulatory standards including GMP quality management systems (e.g. ISO 13485) and operations within the regulated medical device environment (e.g. IVDD, IVDR, FDA 21 CFR 800 series, FDA 21 CFR Part 11).

Preferred Qualifications

• Solid technical proficiency in standard laboratory techniques and equipment operation.
• Ability to analyze data, identify issues, and communicate findings clearly.
• Strong organizational and problem-solving skills with attention to detail.
• Effective communication skills, both written and verbal.
• Ability to work both independently and collaboratively within a team environment.
• Familiarity with laboratory documentation systems, data management tools, and reporting processes.
• Knowledge of laboratory safety practices, compliance requirements, and quality standards.