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Cell Associate Jobs in Maryland (NOW HIRING)

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Cell Therapy Specialist

Frederick, MD · On-site

Cell Therapy Specialist I (Contract) Location: Frederick, MD IMPORTANT: For the first 8-10 weeks of ... Associates Degree in Life Sciences Field with 1+ years of biotech experience or • High School ...

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Cell Associate information

What is the difference between Cell Associate vs Laboratory Technician?

AspectCell AssociateLaboratory Technician
Required CredentialsHigh school diploma or equivalent; some roles may require certification in cell culture techniquesHigh school diploma or equivalent; often requires technical certification or associate degree
Work EnvironmentBiotech or pharmaceutical labs, focusing on cell culture and sample preparationGeneral laboratory settings, performing tests and sample analysis across various fields
Employer & Industry UsageBiotech, pharmaceutical, research institutionsHealthcare, research, manufacturing, and testing labs

While both roles involve laboratory work, a Cell Associate primarily focuses on cell culture and biological sample preparation within biotech and pharmaceutical settings. A Laboratory Technician has a broader scope, performing various tests and analyses across multiple industries. The roles often require similar certifications but differ in specific technical skills and daily tasks.

What are Cell Associates?

Cell Associates are professionals who typically work in manufacturing or laboratory environments, assisting in the production, assembly, or quality control of products, often within a 'cell' or designated work area. Their responsibilities can include operating machinery, inspecting materials, following safety protocols, and maintaining documentation. This role often requires attention to detail, the ability to follow standard operating procedures, and good teamwork skills. Cell Associates play a key part in ensuring that production lines run smoothly and efficiently while maintaining product quality.

What are the key skills and qualifications needed to thrive as a Cell Associate, and why are they important?

To thrive as a Cell Associate, you need a solid understanding of manufacturing processes, attention to detail, and often a high school diploma or equivalent. Familiarity with production equipment, quality control systems, and safety protocols is typically required, with additional training or certifications in lean manufacturing or Six Sigma being advantageous. Strong teamwork, problem-solving abilities, and effective communication help individuals excel in this role. These skills and qualities are essential for maintaining production efficiency, ensuring product quality, and supporting a safe and collaborative work environment.

What are the typical daily responsibilities of a Cell Associate in a manufacturing environment?

A Cell Associate typically works within a production cell, focusing on assembling, inspecting, and packaging products according to standardized procedures. Daily responsibilities often include setting up workstations, operating machinery, maintaining quality control, and collaborating with team members to achieve production targets. Cell Associates are also expected to follow safety protocols, report equipment issues, and participate in continuous improvement initiatives. The role requires attention to detail, adaptability to changing priorities, and effective communication within a team-oriented environment.
What cities in Maryland are hiring for Cell Associate jobs? Cities in Maryland with the most Cell Associate job openings:
Cell Associate jobs near you

hESC Associate Scientist_Scientist levels I or II

Workforce Genetics

Germantown, MD

Full-time

Posted 16 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.