Assess genomic stability through karyotyping and related assays. * Analyze experimental data using appropriate software and statistical tools (e.g., FlowJo, ImageJ, GraphPad Prism, etc.). * Design ...
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Assess genomic stability through karyotyping and related assays. * Analyze experimental data using appropriate software and statistical tools (e.g., FlowJo, ImageJ, GraphPad Prism, etc.). * Design ...
Karyotyping information
What is karyotyping?
A Karyotyping job involves analyzing chromosomes in cells to detect genetic abnormalities or variations. Professionals in this role prepare cell samples, use staining techniques, and examine chromosomes under a microscope. They may work in clinical laboratories, research institutions, or genetic testing facilities. The results help diagnose genetic disorders, guide treatment decisions, and support medical research. Strong attention to detail and knowledge of genetics are essential for this role.
What are the typical responsibilities of someone working in karyotyping?
Professionals in karyotyping are responsible for preparing, staining, and analyzing chromosome samples under a microscope to detect genetic abnormalities. Daily tasks include processing patient samples, operating imaging systems, interpreting test results, and maintaining accurate laboratory records. Karyotypists often collaborate with genetic counselors, pathologists, and laboratory technologists to provide detailed results that inform patient diagnosis and treatment options. The work is detail-oriented and vital for supporting clinical decision-making in genetics, oncology, and prenatal care.
What are the key skills and qualifications needed to thrive in the karyotyping position, and why are they important?
To thrive in karyotyping, you need a background in genetics, cytogenetics, or a related biological science, typically with laboratory experience and a relevant degree or certification. Familiarity with microscopes, imaging software, and specialized laboratory equipment is essential, and certification such as ASCP in cytogenetics is often preferred. Attention to detail, analytical thinking, and effective communication are important soft skills for accurate analysis and collaborative reporting. These abilities ensure reliability and precision in detecting chromosomal abnormalities, which is crucial for accurate diagnostics and patient care.
How long does it take to become a karyotyping technologist?
Becoming a karyotyping technologist typically requires completing a bachelor's degree in medical laboratory science or a related field, which takes about four years. Additionally, specialized training in cytogenetics and certification, such as from the American Society for Clinical Pathology (ASCP), may take several months to a year, making the total pathway approximately 4 to 5 years.
Who performs karyotyping?
Karyotyping is performed by trained cytogenetic technologists or laboratory scientists in medical laboratories. These professionals prepare and analyze cell samples, often using microscopes and specialized staining techniques, to detect chromosomal abnormalities. Certification and knowledge of laboratory procedures are typically required for this role.
What are popular job titles related to Karyotyping jobs in Washington?
For Karyotyping jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Karyotyping jobs in Washington look for?
The top searched job categories for Karyotyping jobs in Washington are:
What cities in Washington are hiring for Karyotyping jobs?
Cities in Washington with the most Karyotyping job openings:
Full-time
Re-posted 12 days ago
Job description
Embryonic Stem Cell Associate Scientist/Scientist I/II
Our client is seeking a highly skilled Associate Scientist/Scientist to contribute to their efforts in embryonic stem cell biology and early development processes. This role involves hands-on work with human pluripotent stem cells, development of differentiation protocols and stem cell-based solutions, and application of advanced analytical methods to study lineage specification and embryogenesis. The successful candidate will design, execute, and optimize experiments, interpret complex datasets, and collaborate closely with multidisciplinary teams to advance our scientific and translational objectives, deepen our understanding of embryonic stem cell development, facilitate next-generation therapeutic platforms, and help drive high-quality, reproducible science in a fast-paced, cross-functional environment.
Education:
- BS/MS in Stem Cell Biology, Developmental/Cell Biology, Embryology, Molecular/Cell Biology, Reproductive Biology, or related fields. A master’s degree is preferred. Ph.D.’s with requisite experience will also be considered for this position.
- 3+ years of relevant industry experience.
- Prior experience in biotech, GMP, or regulated lab environments is strongly preferred.
- Demonstrated expertise in applied research, translational projects, process development, and a strong product‑oriented approach.
- Certification as a stem cell professional (CSCP) is optional but not a requirement.
Responsibilities:
- Expand and maintain human embryonic stem cells (hESCs) under feeder-free and feeder-based conditions, including media optimization and validation.
- Develop 2D and 3D (organoid) cell cultures.
- Ensure stable pluripotency, perform routine passaging, and prevent spontaneous differentiation.
- Execute and optimize differentiation protocols into specific lineages (endoderm, mesoderm, ectoderm).
- Perform colony picking, clonal expansion, and establish new and stable hESC lines.
- Scale up hESC cultures from research grade to clinical grade production (suspension, bioreactors, automation-ready systems).
- Apply knowledge of early embryo development (cleavage to blastocyst), germ layer formation, and lineage specification.
- Characterize stem cells using flow cytometry for pluripotency and lineage markers. Potency assay development. Immunostaining assays. qPCR, and gene expression profiling. Protein assays (Western blotting and ELISA). Fluorescence or confocal microscopy and live-cell imaging. Single-cell RNA-Seq and other omics platforms.
- Assess genomic stability through karyotyping and related assays.
- Analyze experimental data using appropriate software and statistical tools (e.g., FlowJo, ImageJ, GraphPad Prism, etc.).
- Design, express, and troubleshoot mRNA constructs; perform transfections for transient gene expression, optimize delivery methods for high efficiency, isolate clones, and express and validate encoded proteins in hESCs.
- Create and maintain master and working cell banks.
- Conduct QC assays for viability, identity, sterility, and contamination control (e.g., bacteria, mycoplasma).
- Optional: Optimize culture system, differentiation protocols under defined conditions, and assay workflows.
- Work within GLP/GMP guidelines for stem cells and their derived products when applicable.
- Ensure compliance with ethical and regulatory requirements for hESC research.
- Design, execute, and troubleshoot complex experiments independently.
- Maintain accurate lab notebooks and documentation, and follow SOPs and quality systems.
- Present data clearly in meetings, reports, and cross-functional reviews.
- Lead independent research projects and contribute to scientific strategy.
- Support white paper/manuscript preparations and conference presentations as needed.
Technical expertise:
- Experience with translational research or clinical trials involving embryonic stem cells and developmental embryology.
- Proficient in the isolation and derivation of hESC lines, characterization using analytical and molecular assays, and karyotyping/genomic stability analysis.
- Familiarity with key signaling pathways, including Wnt, BMP, FGF, TGF-b.
- Knowledgeable in clonal isolation, screening, and validation; transfection and transduction methods; and cryopreservation, thawing, stability testing, and recovery of hESCs.
- Strong understanding of ethical guidelines overseeing hESC research.
- Familiarity with Institutional Review Board (IRB) processes and institutional compliance requirements.
- Knowledge of national and international stem cell regulations (NIH and FDA guidelines) and regulatory expectations for clinical grade ESC/iPSC products (identity, purity, potency assays).
- Experienced in contributing to IND-supporting studies and ethical compliance in human and animal research.
- Understanding of FDA regulatory frameworks, CMC and batch records, and SOP development, optimization, and documentation.
- Strong collaboration skills with various teams and clear, effective scientific communication, including data presentation and detailed reporting.
- Demonstrated problem-solving ability and expertise in troubleshooting complex experimental workflows.
- Experience mentoring junior scientists or technicians.
- Exceptional attention to detail, essential for embryonic stem cell workflows.
- Ability to present research outcomes and contribute to white papers/manuscripts.
- Demonstrate project management capabilities and work within timelines and budgets.
- Proficient in aseptic techniques and experienced working in BSL-2 environments.
- Competence in experimental design and data analysis.