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Associate Scientist Cell Line Development Jobs in North Carolina

Position Summary Seeking a highly motivated and detail-oriented Associate Scientist to join our ... development, utilizing strong scientific expertise and knowledge of adeno viral vector and cell ...

Position Summary Seeking a highly motivated and detail-oriented Associate Scientist to join our ... development, utilizing strong scientific expertise and knowledge of adeno viral vector and cell ...

Analytical support * Lead the development and implementation of phase-appropriate analytical ... ddPCR, ELISA, cell-based potency assays, NGS, HPLC, and AUC, driving method evolution ...

Analytical support * Lead the development and implementation of phase-appropriate analytical ... ddPCR, ELISA, cell-based potency assays, NGS, HPLC, and AUC, driving method evolution ...

Possess full knowledge of setup/change over of all equipment within the cell/line, and perform them ... Dauch will not discriminate against any Associate or applicant for employment because of age, race ...

As an Associate Scientist, Analytical Chemistry at our Durham facility. A typical day will include ... Execute stability studies to support the development of new drug substances or drug products.

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Associate Scientist Cell Line Development information

What are some common challenges faced by associate scientists in cell line development, and how can they be addressed?

Associate Scientists in Cell Line Development often encounter challenges such as optimizing cell growth conditions, maintaining cell line stability, and troubleshooting low productivity or contamination issues. Addressing these challenges requires strong attention to detail, effective documentation, and collaboration with cross-functional teams such as upstream process development and quality control. Regular communication with senior scientists and participation in team meetings can also help in problem-solving and ensuring project timelines are met. Staying updated on the latest techniques and technologies in cell line engineering further supports overcoming these obstacles.

What does an associate scientist in cell line development do?

An Associate Scientist in Cell Line Development is responsible for creating and optimizing cell lines that are used in the production of biopharmaceutical products. Their work involves culturing cells, performing genetic modifications, and conducting experiments to select the best cell lines for manufacturing proteins or other biologics. They also document their findings, analyze data, and collaborate with other scientists to ensure the cell lines meet regulatory and quality standards. This role is vital in the early stages of drug development, as robust cell lines are essential for consistent and scalable production.

What is the difference between Associate Scientist Cell Line Development vs Associate Scientist Bioprocess Development?

AspectAssociate Scientist Cell Line DevelopmentAssociate Scientist Bioprocess Development
Required CredentialsBachelor's or Master's in Life Sciences, Molecular Biology, or related fieldsBachelor's or Master's in Biotechnology, Chemical Engineering, or related fields
Work EnvironmentLaboratory focused on cell line creation and characterizationLaboratory and pilot plant focused on process scale-up and manufacturing
Employer & Industry UsageBiotech and pharmaceutical companies developing cell lines for biologicsBiotech and pharma companies optimizing bioprocesses for production

Associate Scientist Cell Line Development primarily focuses on creating and characterizing cell lines for biologic production, while Associate Scientist Bioprocess Development concentrates on scaling up and optimizing manufacturing processes. Both roles require similar educational backgrounds and are essential in biologics development, but they differ in their specific focus within the biopharmaceutical pipeline.

What are the key skills and qualifications needed to thrive as an associate scientist in cell line development?

To thrive as an Associate Scientist in Cell Line Development, you need a strong background in cell biology, molecular biology, and protein expression, typically supported by a relevant science degree. Familiarity with technical tools such as flow cytometry, cell culture systems, CRISPR gene editing platforms, and data analysis software is essential. Attention to detail, strong problem-solving abilities, and effective teamwork are standout soft skills in this role. These skills ensure high-quality cell line generation, reproducible results, and successful collaboration in fast-paced biopharmaceutical environments.

What cities in North Carolina are hiring for Associate Scientist Cell Line Development jobs?

Cities in North Carolina with the most Associate Scientist Cell Line Development job openings:

Full-time

Posted 14 days ago


Job description

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.

Our vision: Pioneering science to create transformative molecular medicines.

Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.

Our principles:

  • Advance innovative science by pushing boundaries.

  • Bring transformative therapeutics to patients in need.

  • Provide an environment for employees to reach their fullest potential.

Our values:

  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.

  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.

  • Embrace Responsibility. We are humbled by the enormity of our mission.We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.

  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.

  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

Position Summary

Seeking a highly motivated and detail-oriented Associate Scientist to join our Bioanalytical Group.

The successful candidate will play a key role in developing and validating binding antibody and neutralizing antibody assays performed on preclinical and clinical samples to support our gene therapy programs. This position requires hands-on experience in immune assay techniques and a basic understanding of gene therapy research. The successful candidate will work closely with cross-functional teams to ensure that assays meet regulatory standards and contribute to the advancement of gene therapy projects. The ideal candidate will have a strong background in binding antibody assays, cell culture, and aseptic techniques. This position offers an opportunity to work in a dynamic, fast-paced environment and contribute to the development of innovative gene therapies for patients in need. Antibody assay development, qualification and validation activities will be performed in compliance with GCLP (Good Clinical Laboratory Practices) laboratories, GLP (Good Laboratory Practices), CLIA (Clinical Laboratory Improvement Act), and national, international, and state regulations.

This position is on site in RTP, NC and reports to an Associate Director, Clinical Immunology.

Job Responsibilities

  • Independently design and execute complex assays related to neutralizing and total antibody development, utilizing strong scientific expertise and knowledge of adeno viral vector and cell-based techniques

  • Optimize and troubleshoot experimental protocols to ensure accuracy, reproducibility, and efficiency. Perform neutralizing and total antibody assay validation to meet FDA and CLIA guidelines

  • Perform clinical sample analysis and prepare comprehensive reports for clinical sites

  • Perform in-depth data analysis using advanced statistical and bioinformatics tools, and draw meaningful conclusions from the results

  • Prepare comprehensive reports, presentations, and manuscripts summarizing research findings for internal and external stakeholders

  • Stay current with the latest advancements in gene therapy research and apply this knowledge to your work

  • Collaborate effectively with research scientists, engineers, and other team members to achieve project goals

  • Develop and implement standard operating procedures (SOPs) for maintaining consistent research quality

  • Assist with the preparation and submission of regulatory filings

  • May supervise and mentor junior research staff

Minimum Requirements

  • Bachelor's degree in Immunology, Biology, Biochemistry, Biotechnology, Virology or related field with 8+ years' relevant work experience; or Master's degree in Immunology, Biology, Biochemistry, Biotechnology, Virology or related field with 4+ years' relevant work experience

  • Prior experience in Pharma or CRO industry

  • Basic lab skills, such as adhering GCLP, biosafety and chemical use guidelines (training provided) and making reagents at desired dilutions or concentrations

  • Demonstrated experience in the performing development and validation of ligand binding and neutralizing antibody assay following GLP compliance

  • Experience with mammalian cell culture and performing analytical assays using MSD platform

  • Knowledge of industry practices for the development, qualification/ validation of immunogenicity assays and FDA guidelines

  • Knowledge of Companion Diagnostics

  • Proficiency with MS Office tools (Word, Excel, and PowerPoint)

  • Self-motivated, organized, and individual capable of working independently as well as an active team contributor

  • Strong oral and written communication skills

  • Excellent interpersonal skills with the ability to interact effectively with teams, internally and externally

Preferred Education, Experience and Skills

  • Experience in performing Western blots and protein purification. and processing/handling primary cells such as PBMCs

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid jobrelated requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at careers@askbio.com.

Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.