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Jobs

System MAC Movement Scientist Shriners Hospitals for Children

System MAC Movement Scientist
Philadelphia, Pennsylvania

Reporting to the Corporate Director of Motion Analysis Center, the role collaborates with system-wide research, engineering, and therapy teams to develop research initiatives, quality improvement programs, business plans, and new clinical services. The Motion Analysis Center Manager/Scientist (MACMS) is a research and clinical innovation leader responsible for advancing motion analysis services, improving patient outcomes, and supporting evidence-based care across Shriners Children's.

19 days ago

Scientist I Campbell's

Scientist I
Camden, New Jersey

Our portfolio includes the iconic Campbell’s brand, as well as Cape Cod, Chunky, Goldfish, Kettle Brand, Lance, Late July, Pacific Foods, Pepperidge Farm, Prego, Pace, Rao’s Homemade, Snack Factory, Snyder’s of Hanover. This role partners closely with Product Development, Quality, Regulatory, Procurement, Supply Chain, and external suppliers to identify, evaluate, and commercialize flavor solutions that delight consumers and meet business objectives.

20 days ago

Associate Scientist Temple University

Associate Scientist
Philadelphia, Pennsylvania
  • $60,000–$67,000

Experience with induced pluripotent stem cell culture and differentiation, quantitative confocal microscopy, proteomics, molecular biology skills (such as molecular cloning, ChIP-seq, DNA FISH, and RNA FISH), recombinant viral tools (such as lentivirus, retrovirus, and adenovirus). The Associate Scientist works in the Gan Lab on ongoing projects focusing on transcriptional condensates and their roles in regulating cardiovascular cell lineage specification and cell fate transition during development and disease.

30+ days ago

PT Research Scientist Temple University

PT Research Scientist
Philadelphia, Pennsylvania
  • $32 / hour

Oversight of program research initiatives including: -Evaluating and implementing interventions that promote community participation of adults with schizophrenia-spectrum disorders, bipolar disorder, or major depression, or autistic adults (e.g., work, housing, education, leisure/recreation, spirituality); -Translational research that examines strategies for enhancing the uptake of evidence-based practices in community mental health settings; -Research that examines factors that may affect community participation, cognitive functioning, or other mental health outcomes; Specific knowledge of research on caregiver perspectives on inclusion and participation and on racial and ethnic factors that influence participation; and. *Supervising up to two Center research staff; *Writing research publications and grant proposals in partnership with Center faculty; *Assistance in overseeing Center studies; *Providing training and technical assistance related to Center activities; *Additional similar undertakings associated with having a productive and successful research career.

30+ days ago
New

Associate Principal Scientist - ADME Cyprotex

Associate Principal Scientist - ADME
Princeton, New Jersey

Ability to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new ADME assays as well as contribute to the continuous improvement of the current ADME assays.

2 days ago

Scientist, Quality Control (2Nd/3Rd Shift) Orca Bio

Scientist, Quality Control (2Nd/3Rd Shift)
Princeton, NJ
  • $70,000–$90,000 / year

Production Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment. The Scientist, Quality Control conducts routine and non-routine analysis, including but not limited to biochemical and chemical analysis of processes leading up to drug product according to established operating procedures.

30+ days ago

Upstream Principal Scientist, Vector Biology Legend Biotech Corp

Upstream Principal Scientist, Vector Biology
Philadelphia, PA
  • $146,410–$192,164 / year

The Principal Scientist will bring a rare combination of molecular biology depth and bioprocess engineering breadth, functioning as a key technical authority who bridges construct-level design decisions with upstream process outcomes, while closely interfacing with Downstream, Analytical, and Technical Development partners to ensure end-to-end process coherence and readiness for technology transfer. Exemplary oral and written communication skills, with the ability to translate complex early process development findings into compelling scientific narratives for diverse audiences including R&D leadership, CMC colleagues, and cross-functional program teams while operating with equal effectiveness as a self-directed scientific contributor and an engaged collaborative partner.

30+ days ago

Scientist Legend Biotech Corp

Scientist
Philadelphia, PA
  • $96,267–$126,351 / year

Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. This Scientist position will closely work with Molecular Biology, Downstream, Analytical and Technical development partners to ensure end-to-end process alignment, support comparability strategy and readiness, and enable efficient, high-quality technology transfer.

26 days ago

Upstream Principal Scientist, Vector Biology Legend Biotech US

Upstream Principal Scientist, Vector Biology
Philadelphia, PA

The Principal Scientist will bring a rare combination of molecular biology depth and bioprocess engineering breadth, functioning as a key technical authority who bridges construct-level design decisions with upstream process outcomes, while closely interfacing with Downstream, Analytical, and Technical Development partners to ensure end-to-end process coherence and readiness for technology transfer. Working knowledge of downstream processing operations —encompassing harvest and clarification strategies, affinity and ion-exchange chromatography, and tangential flow filtration — with the scientific acuity to incorporate purification process requirements and vector quality attribute targets into upstream process design; experience in integrated upstream-downstream process development is preferred.

30+ days ago

Scientist Legend Biotech US

Scientist
Philadelphia, PA
  • $96,267–$126,351 / year

Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. This Scientist position will closely work with Molecular Biology, Downstream, Analytical and Technical development partners to ensure end-to-end process alignment, support comparability strategy and readiness, and enable efficient, high-quality technology transfer.

26 days ago

Principal Research Scientist - Frontier Industrial AI AVEVA Group Plc

Principal Research Scientist - Frontier Industrial AI
Philadelphia, PA
  • $213,500–$355,500 / year

This pay range represents the minimum and maximum compensation that the position offers, and final compensation can vary within the range depending on work location, job experience, skills, and relevant educational attainment and/or training. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life - such as energy, infrastructure, chemicals, and minerals - safely, efficiently, and more sustainably.

19 days ago
New

Senior Principal Scientist, Biologics Discovery Process Research Integrator – Protein Expression and Scale-Up 6084-Janssen Research & Development Legal Entity

Senior Principal Scientist, Biologics Discovery Process Research Integrator – Protein Expression and Scale-Up
Spring House, Pennsylvania

Analytical Reasoning, Biochemistry, Biotechnology, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Collaboration, Data Synthesis, Drug Discovery Development, Molecular Diagnostics, Pharmacovigilance, Process Improvements, Productivity Planning, Program Management, Scientific Research, Tactical Planning, Technical Credibility The role will provide integrative technical leadership grounded in mammalian expression, cell line development, and scale-up expertise, ensuring that expression feasibility, manufacturability, productivity, product quality, and scalable production considerations are incorporated into molecule selection, material supply planning, and program strategy.

6 days ago

Principal Scientist, Clinical Biomarker, Immunology & Immuno-Oncology (Hematology) Legend Biotech Corp

Principal Scientist, Clinical Biomarker, Immunology & Immuno-Oncology (Hematology)
Somerset, NJ
  • $146,410–$192,164 / year

Leverage advanced single-cell technologies (e.g., scRNA-seq) to deeply profile immune cell compartments, particularly T-cell states and exhaustion markers, to inform patient stratification and biomarker hypotheses. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases.

30+ days ago

Scientist – Quality Control (QC) Ardena

Scientist – Quality Control (QC)
Somerset, New Jersey

This role supports pharmaceutical development and commercial manufacturing by performing analytical testing of raw materials, in-process materials, finished products, and stability samples within a GMP-regulated laboratory environment. Ardena provides integrated services spanning drug substance development, drug product formulation, GMP manufacturing, bioanalytical services, clinical logistics, fill and finish, and CMC regulatory support.

30+ days ago

Scientist - Site Based, Princeton, NJ Evotec

Scientist - Site Based, Princeton, NJ
Princeton, New Jersey

BA/MS or equivalent experience in a relevant Biological or Chemical scientific discipline with at least 5 years plus experiences working within industry (pharma or CRO). We are seeking a Scientist to be responsible for routine screening of compounds in various in vitro ADME assays and maintaining mammalian cells.

30+ days ago

Associate Director, Patient Safety Scientist Bristol Myers Squibb

Associate Director, Patient Safety Scientist
Princeton, NJ
  • $150,300–$182,125 / year

Responsible for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development, support Structured Benefit Risk, and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance, including collaboration with Epidemiology on risk minimization effectiveness, non-interventional research (NIR) activities for post-authorization safety studies (PASS). The Associate Director, Patient Safety Scientist, is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks.

30+ days ago

HTP Analytical QC Associate Scientist GenScript ProBio

HTP Analytical QC Associate Scientist
Piscataway, New Jersey
  • $60,000–$75,000 / year

Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products.

30+ days ago
Johnson & Johnson logo

Principal Scientist, Product Characterization - Advanced Therapies Johnson & Johnson

Principal Scientist, Product Characterization - Advanced Therapies
Spring House, PA

Required Skills: Preferred Skills: Analytical Reasoning, Biochemistry, Biotechnology, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Coaching, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Organizing, Pharmacovigilance, Presentation Design, Process Improvements, Productivity Planning, Scientific Research. D. or equivalent advanced degree in Biochemistry, Immunology, Virology, Biological Science, or a related field with 3+ years of proven experience in biopharmaceutical development OR a Bachelor's or Master's degree with 6-8 years of relevant experience is required.

20 days ago

Principal Scientist, Cell Line Genome Engineering Bristol Myers Squibb

Principal Scientist, Cell Line Genome Engineering
Princeton, NJ
  • $135,800–$164,563 / year

Extensive hands-on and strategic experience with CRISPR-based genome engineering technologies (e.g., Cas9, Cas12a, dCas9, base-editing, prime-editing and related systems), and gene delivery methods (lentiviral, AAV, electroporation, transposon), with a proven track record of leveraging these tools to build, scale, and optimize cellular models that advance discovery programs. Demonstrated expertise in the design and generation of genetically engineered cellular systems (e.g., knockouts, knock-ins, targeted insertions, overexpression) using a range of approaches including CRISPR-based editing, viral delivery systems, and transposon-based technologies, with the ability to apply these strategically to drug discovery challenges.

11 days ago

Clinical Scientist Systimmune

Clinical Scientist
Princeton, NJ
  • Full time

Work in close collaboration with the clinical team to ensure translation of the clinical protocol (and amendments) into operational deliverables, including but not limited to performing ongoing review and analysis of clinical study data and preparing/reviewing study plans (i.e., Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines, etc.). This role provides an excellent opportunity to gain hands-on experience in clinical trial design and execution while working alongside experienced clinical development professionals in a dynamic biotech/pharmaceutical environment.

30+ days ago
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