Associate Scientist, BioPharma Molecular

Performing critical work that impacts our industry and our world's health while problem solving and innovating in the field - that is what Associate Scientists at KCAS Bio get to do every day.

If that gets you excited too, then maybe working as an Associate Scientist at KCAS Bio is the role for you.

When you work as an Associate Scientist on the Molecular team, you get to further our mission by designing, developing, validating, and analyzing samples utilizing molecular and cell biology techniques such as qPCR, ddPCR and cell-based assays within a GLP (Good Laboratory Practice) environment laboratory environment.

Our Molecular lab team uses a full range of services and viral vector capabilities to analyze gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation.
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In this role, we will rely on you to:


* Demonstrate technical and scientific skills in molecular technologies, including PCR (qPCR and ddPCR) and handling DNA/RNA


* Experience with procedures for the extraction and quantification of nucleic acids


* Experience working with human blood, primary cells/tissue, and derived cell culture skills at the BSL-II level


* Experience with cell culture is preferred


* Plan and carry out assigned experiments.

Including method development, method validation, sample analysis, data calculation, interpretation & review, and troubleshooting


* Design experiments & evaluate outcomes versus current SOPs, protocols, and other relevant standards.

Recommend appropriate course of action as necessary


* Act as lead scientist and provide work instructions and technical training to more junior scientific staff in conducting assigned projects


* Perform all aspects of the job in a way that supports the company brand, mission, vision, and values

To qualify specifically for this role, you will have:


* Bachelor's, Masters or PhD in microbiology, biochemistry, chemistry, immunology, or related field with 4 years' experience in a scientific laboratory environment


* Experience with design, method development, validation, and sample analysis


* Experience with GLP requirements and Good Documentation Practices (GDP)


* Manage material, equipment, and instrumentation


* Analyze and interpret data, prepare summary tables, and review raw data


* Assist with the preparation and review of SOPs, study plans, and reports


* Ability to multi-task and meet deadlines


* Excellent verbal and written communication and organizational skills


* Self-motivated and driven


* Flexible and adaptable - able to work independently and/or in a team environment


* Ability to troubleshoot and problem-solve - Critical Thinking

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(Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position.

Employees must follow instructions and perform additional duties as requested.)

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