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Associate Ipsc Jobs in Frederick, MD (NOW HIRING)

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Associate Ipsc information

See Frederick, MD salary details

$10

$15

$18

How much do associate ipsc jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for associate ipsc in Frederick, MD is $15.33, according to ZipRecruiter salary data. Most workers in this role earn between $14.33 and $15.77 per hour, depending on experience, location, and employer.

What is the difference between Associate Ipsc vs Security Analyst?

AspectAssociate IpscSecurity Analyst
CertificationsTypically requires basic security certifications like CompTIA Security+ or equivalentOften requires advanced certifications such as CISSP, CISA, or Security+
Work EnvironmentEntry-level security operations, monitoring, and support roles within organizationsMore analytical roles involving threat assessment, incident response, and security strategy
Employer & Industry UsageUsed in various industries for initial security support rolesCommon in cybersecurity firms, large corporations, and government agencies

The Associate Ipsc role is typically an entry-level position focusing on security support and monitoring, requiring basic certifications. In contrast, a Security Analyst handles more complex security analysis and incident response, often requiring advanced certifications and experience. Both roles are essential in cybersecurity, but they differ in responsibilities and expertise level.

What are the key skills and qualifications needed to thrive as an associate IPSC?

To thrive as an Associate IPSC (Integrated Primary and Secondary Care), you typically need a background in healthcare or life sciences, strong analytical skills, and familiarity with patient care processes. Knowledge of healthcare data management systems, electronic medical records, and possibly certifications in healthcare administration or clinical research are often required. Excellent communication, attention to detail, and strong organizational skills help Associates effectively coordinate care and collaborate within multidisciplinary teams. These skills ensure efficient healthcare delivery, accurate data management, and improved patient outcomes in integrated care environments.

What are the typical responsibilities and collaborative expectations for an associate IPSC?

As an Associate in an IPSC environment, you can expect a dynamic blend of clinical and administrative responsibilities. Your daily tasks may include assisting with patient intake, supporting physicians with documentation, and facilitating communication between primary and specialty care teams. Collaboration is key, as you'll work closely with nurses, providers, and administrative staff to ensure seamless patient care and efficient clinic operations. This role often offers opportunities to learn about various specialties and can serve as a strong foundation for career advancement within healthcare administration or clinical practice.

What is an associate IPSC?

Associate IPSCs, or Associate Induced Pluripotent Stem Cell researchers, are professionals who support research and development involving induced pluripotent stem cells. Their work typically includes culturing cells, maintaining lab equipment, assisting with experiments, and documenting results. They play a key role in advancing regenerative medicine, disease modeling, and drug discovery. Associate IPSCs often work under the supervision of senior scientists and contribute to publication-quality research.
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Associate Ipsc jobs near you

hESC Associate Scientist_Scientist levels I or II

Workforce Genetics

Germantown, MD

Full-time

Posted 29 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.