Research Scientist Jobs in Readington, NJ
- 609 JobsAssociate Formulation Scientist
Then this Associate Formulation Scientist opportunity could be the right fit for you. This exciting opportunity as an Associate Formulation Scientist offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance, paid PTO etc. $50k-55k yearly2d agoTranslational Bioinformatics Research Scientist
Project Description: Our client is seeking a passionate scientist to join their Disease Strategy and Late-Stage Hematology team in the Translational Bioinformatics group. $89k-130k yearly est.6d agoScientist 2 - Research and Development (contract)
Location: Raritan, NJ $79k-109k yearly est.5d agoEngineering - Assistant/Associate Scientist
Job Location: Summit, NJ www.onboardusa.com On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. The Assistant/Associate Scientist contract position will be in the Downstream Process Development group in Summit, NJ, and be responsible for the development of scalable purification processes, process characterization, Tox material production, and tech transfer to GMP facilities for clinical/commercial manufacturing. On-Board Scientific is hiring an Assistant/ Associate Scientist in Summit, NJ! Today, On-Board is a thriving privately held family of companies with services including Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America. The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. $41.9-43.2 hourly23d agoEngineering - Senior Associate Scientist
Job Description: Senior Scientist Warren, NJ This role is 100% Onsite Summary As part of the Product Sciences group, the energetic and motivated Sr Scientist/Scientist will have responsibility for making significant contributions the development of scientific strategy that informs the design, execution, and interpretation of complex experiments/studies related to generation of new/enhanced knowledge regarding cellular immuno-oncology-based products, intermediates, starting materials, manufacturing processes and analytical tools within a CMC technical development function. The Sr Scientist/Scientist will be tasked to independently drive achievement for critical program, platform, and functional objectives in collaboration within technical development teams across the Cell Therapy Development space, and key areas of the Cell Therapy franchise including research and translation development, informatics, and biostatistics organizations. To achieve these objectives, the Sr Scientist/Scientist will be expected to develop and implement scientific mentorship and leadership skills and capabilities in the direct or matrixed management of small teams. Responsibilities will include, but are not limited to, the following: Contribute to the development of integrated scientific/technical strategy to inform the development of biological hypotheses relating to product cellular attributes and their impact on clinical outcomes, manufacturing and development of analytical tools Contribute to or lead technical development of sensitive bioanalytical assays to characterize cell products, intermediates and starting material Operate effectively within and drive cross-functional collaborations to develop and execute complex characterization strategies relating to clinical and non-clinical product development Support CMC objectives by providing biological and technical knowledge across program and platform strategies for product, process and analytical development Efficiently organize data, integrate concepts and share within, across teams with appropriate level of complexity/details based on audience Proactively support expansion of general knowledge within cell therapy development function and maintain awareness of competitive landscape in the cellular immuno-oncology space Actively engage in the development, growth, career planning, and empowerment of individuals and teams through deliberate and thoughtful strategies and work to provide an optimal environment within which teams and individuals can flourish Reinforce safe workplace practices in accordance with company and OSHA policies/procedures Skills/Knowledge Required Ph.D. or M.S. in Immunology, Cell/Molecular Biology, Biomedical Engineering or related discipline with demonstrated track/record of experience leading teams to achieve objectives in academic and/or industrial settings (0-5 years for Ph.D./, 5-10+ years for M.S.) Demonstrated ability in achieving objectives and deliverables on time with high quality Strong desire to work within a team structure and to develop, mentor and coach team members leading to their operational, success, engagement, growth, and development is Required Ability to work under minimal technical supervision, perform technical, strategic and operational tasks independently and lead complex and cross-functional activities Ability/willingness to identify and surface both risk and opportunity Extensive experience in mammalian cell culture techniques, including isolation of immune cell subsets, maintenance and expansion of primary cells and cell lines is required Advanced knowledge of basic techniques in immunology, cell biology and molecular biology Is Required. Experience With FACS, Immunofluorescence-based Assays, ELISA, PCR, cytokine and chemokine detection, cell-based bioassays is highly desired Experience with analytical method development for a variety of cell-based bioassays, binding assays and/or residual impurities assays is preferred Motivation and drive to acquire new skills and knowledge is desired Willingness to work in a regulated industrial environment. Excellent verbal and written communication skills $72k-112k yearly est.21d agoAssociate Director Clinical Research Scientist
A strong company culture commitment to their development they are actively seeking an Associate Director Clinical Research Associate. Minimum of 8 years of experience in clinical research with at least 4 or more years of drug development experience $73k-123k yearly est.2d agoStaff Scientist
Peak Environmental, A Nova Group, GBC Company $81k-122k yearly est.9d agoAssociate Scientist
Synbio Technologies is looking for an Associate Scientist to join the production team, which focuses on developing and commercializing gene synthesis and sequencing platforms. This Associate Scientist will collaborate with the Business Development, Project Management, and Marketing team to deliver research projects and launch new products. Synbio Technologies is committed to discovering and developing cutting-edge DNA technologies for the advancement of life science, synthetic biology, drug discovery and development, diagnostics and precision medicine and digital information DNA storages, etc. Synbio Technologies has built a comprehensive DNA reading (sequencing), DNA writing and DNA editing platforms enabling us to aid customers in one-stop DNA solutions. $67k-98k yearly est.19d agoScientist Formulation
Scientist to join the team. $81k-123k yearly est.15d agoSr. Scientist, Coatings
Benjamin Moore & Co., a Berkshire Hathaway company, is a leading manufacturer of innovative, high-quality coatings for the architectural and light-duty industrial maintenance markets. We are currently seeking a Senior Scientist (Coatings Technology) to join our Product Development team. At Benjamin Moore, we believe diversity of culture, talent, and varying perspectives is key to a collaborative, innovative, and successful business. At Benjamin Moore & Co, we don't just accept difference -- we celebrate it, we support it, and we thrive because it benefits our employees, our products, and our community. The Senior Scientist job is an exciting chance to join a team that promotes and recognizes innovation. We hope you will join us and become an advocate for diversity and inclusion here at Benjamin Moore. $125k-158k yearly est.7d agoResearch Associate
Accutar Biotech offers a competitive compensation in industry, friendly and rewarding working and training environment, and excellent growth potential. We are seeking a talented and self-motivated research associate to join our exciting drug discovery effort. Location: Accutar Biotechnology, Cranbury, New Jersey. $58k-93k yearly est.23d agoSr. Scientist
Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Synectics offers eligible employees vision insurance through VSP. Premiums are subsidized by Synectics. Synectics offers eligible employees and their dependents a dental plan through MetLife. Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. $107k-151k yearly est.2d agoPostdoctoral Researcher
The INSPIRE Program is based in the Piscataway Campus of Rutgers and is open to postdocs applying to do research at any Rutgers campus (Newark, Piscataway, New Brunswick, Camden). The Rutgers INSPIRE program is funded by the NIH IRACDA Program to train Postdoctoral Fellows in the Biomedical Sciences who are interested in a successful faculty career $49k-61k yearly est.16d agoSenior Analytical Scientist
The Analytical Scientist will be part of a team of drug development professionals responsible for the continued development and regulatory approval of thin film drug products containing a wide range of therapeutic compounds. $79k-112k yearly est.2d agoPharmaceutical Analytical Scientist/Manager/Director
About Ascendia Pharmaceuticals: Ascendia is a specialty pharmaceutical Research and Development CDMO company dedicated to developing enhanced formulations of existing drug products, and enabling formulations for pre-clinical and clinical stage drug candidates. Ascendia specializes in creating formulations for poorly-water soluble molecules using nano-particle technologies. Ascendia assesses the feasibility of a broad array of formulation options in order to improve a drug's bioavailability and solubility. Ascendia's technologies include nano-emulsions, amorphous solid dispersions, nano-particles, injectable, and oral controlled release. Ascendia provides development and testing services - from discovery-stage molecules to life-cycle-management projects - creating formulation solutions with enhanced biopharmaceutical properties suitable for clinical scale-up. The mission of our company is to provide customized formulation solutions to “salvage” difficult compounds and to create advanced medicines to help patients “prevail” over their disease and enhance quality of life. About the Position: The qualified candidate will take an active role in supporting drug development by applying a variety of analytical methodologies to support physical and chemical characterization of drug substances (including raw materials and intermediates), biologics, and drug products. Working knowledge of analytical (e.g., HPLC-UV, HPLC-MS, GC-MS, spectroscopy) and physical chemical techniques (e.g., particle size, dissolution) used for the characterization of pharmaceutical substances and products is desired. Hand-on experience in HPLC method development and biological characterization is highly desired. Position level varies from bench chemist to principle scientist, depending on experience. Principal Responsibilities: The individual will be responsible for performing laboratory work in support of analytical testing of pharmaceutical projects, and relevant experience with the following analytical methodologies: chromatography, dissolution, KF, particle size will be desirable. Job responsibilities may include analytical method development and validation; stability and release testing; testing to support pharmaceutical development efforts; direct interaction with project team members, including presentation of data; critical review of data; preparation of technical reports; and evaluation of new instrumentation or analytical techniques. The candidate must be able to interact effectively with peers and leaders as part of a multi-disciplinary team and work in a fast-paced environment. Attention to detail, strong organizational skills, the ability to multitask, and effective interpersonal and communication skills are required. Qualifications The position requires a B.S, M.S. or Ph.D. in Pharmaceutical Chemistry, Analytical Chemistry, Biology, Bioengineering, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry. Working knowledge in analytical method development and validation under cGMP environment, esp biological characterization is highly desired. Experience with a wide-variety of software and information systems (e.g. Empower, ChemStation, or LIMS). Experience in problem-solving skills and instrument trouble-shooting. Good oral and written communication skills and the ability to write and review technical reports and scientific papers are desired. Working knowledge of pharmaceutical product development, CMC regulatory requirements, project management; and capability to collaborate with colleagues. EEO/AA M/F/V/D $79k-113k yearly est.16d agoEngineering - Assistant/Associate Scientist
Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. Location: Summit, NJ 07901 At Net2Source, we believe everyone has an opportunity to lead. Title: Engineering - Assistant/Associate Scientist The Assistant/Associate Scientist contract position will be in the Downstream Process Development group in Summit, NJ, and be responsible for the development of scalable purification processes, process characterization, Tox material production, and tech transfer to GMP facilities for clinical/commercial manufacturing. $35-40 hourly23d agoY - Bioinformatics Scientist in Lawrenceville, NJ, US
50%Onsite Senior Research Scientist, Disease Strategy and Late Stage Hematology, Translational Bioinformatics Summary: We are seeking a passionate scientist to join our Disease Strategy and Late Stage Hematology team in the Translational Bioinformatics group. $78k-112k yearly est.6d agoSr. Research Scientist, Translational Bioinformatics
A Pharmaceutical Company is seeking a Sr. Research Scientist, Translational Bioinformatics in Lawrenceville, NJ. Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. Visit the Hays Career Advice section to learn top tips to help you stand out from the crowd when job hunting. Sr. Research Scientist, Translational Bioinformatics - Contract -Lawrenceville, NJ - $48.00-$58.00/hr. Hays is committed to building a thriv This position is a contract/temporary role where Hays offers you the opportunity to enroll in full medical benefits, dental benefits, vision benefits, 401K and Life Insurance ($20,000 benefit). $48-58 hourly2d agoComputational Biologist
Lawrenceville, NJ 23-01401 Job Description: *50%Onsite Senior Research Scientist, Disease Strategy and Late Stage Hematology, Translational Bioinformatics **5+ years of bioinformatics data analysis experience in the Cancer Research setting or Biopharma space Job Description We are seeking a passionate scientist to join our Disease Strategy and Late Stage Hematology team in the Translational Bioinformatics group. This team applies available and innovative bioinformatics, machine learning and statistical approaches to rich integrated patient data to gain insights and empower data-driven decisions. This position will focus on translating insights using patient data to assist with disease stratification, mechanisms of treatment response and resistance in order to derive therapeutic mechanisms of action for existing and Client therapies, as they transition into clinic. The position would suit an individual with good statistical knowledge and computational capabilities, excellent communication, and collaboration skills. Applications are encouraged from those involved in innovative cancer translational biomarker research studies especially heme malignancies. Responsibilities Define and execute data analysis plans to gain insights from multimodal data. Perform NGS data processing, QC, and downstream analysis. Summarize analysis results, write a report. Qualifications: Ph.D. or M.Sc. with 3+ years of experience- in computational biology, bioinformatics, biostatistics, or another relevant field. Experiences in cancer research institutions, biotech or pharmaceutical industries is a plus. Fluency with Linux-based high-performance computing environments, R/Bioconductor, and reproducible research practices specially GitHub. Experiences with other high-level programming language such as Python is a plus. Familiarity with cloud computing environments (Docker, AWS) is highly desired. Experience with RNA-Seq, DNASeq workflow and pipelines. Familiarity with single-cell sequencing and/or spatial data is desirable. Some statistics background is required. Ability to work both independently and collaboratively, and to handle several concurrent, fast-paced projects while conforming with rigorous requirements of clinical studies. Excellent written and oral communication skills, including an ability to explain complex ideas to computational scientists, experimentalists, and clinicians $66k-90k yearly est.10d agoEngineering - Senior Associate Scientist
The Principal/Sr. Scientist conducts product and process characterization studies; collaborates with research and development in drug product process development of sterile parenteral and biologics drug product and works with manufacturing sites to characterize, troubleshoot or optimize processes for lifecycle products. This position is accountable for the design and execution of process characterization to ensure robust parenteral manufacturing processes. This applies to both new products and key life cycle management products. Additional responsibilities may include development of new manufacturing technologies and providing specialized expertise as necessary to complement site capabilities for critical investigations or process improvements. Key Responsibilities Include Execution of post-market process change activities/experiments through partnership with R&D development assets. Characterization, optimization and troubleshooting product and manufacturing processes of parenteral dosage forms. Collaboration with R&D and manufacturing sites to design and execute experiments to support product robustness, new technology implementation, and/or manufacturing investigations Serve as technical resource to other functions, providing expertise on the product and its process. Effectively represent biologics drug product manufacturing science and technology in various internal and external teams and committees on development, technology transfer, manufacturing, specifications, process validations and launch. Provide assistance to sites globally to resolve significant quality events Qualifications Advance degree in the Pharmaceutical or Biotechnology industry in product and process development and commercialization in a global environment with 6 years industry experience for Sr. Scientist or 8 years experience for Principal Scientist. Ph.D. degree preferred. Expertise in parenteral product development and manufacturing Key Skills And Experience Hands-on experience in the laboratory Excellent Skills/experience Working In Cross-functional Teams Understanding of sterile and liquid products, particularly parenteral & biologics commercial manufacturing and associated unit operations. Understanding of primary packaging for parental and/ or lyophilization process is preferred Understanding of Quality by Design (QbD), Design of Experiments (DOE), multivariate analysis, PAT, critical process and material attributes and CQA's. Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS). Able to design and execute scientifically sound, hypothesis driven experiments Skilled in writing and reviewing complex study plans and scientific reports. Possess high level of familiarity with sterile product processing equipment and manufacturing facilities. Overall knowledge of parenteral technology: aseptic processing, sterilization, isolator processing, lyophilization, filter validation, pre-filled syringe operations, etc. Strong understanding of project management systems and tools Six Sigma Green/Black Belt certification desirable $72k-111k yearly est.23d ago
Learn More About Research Scientist Jobs
How much does a Research Scientist earn in Readington, NJ?
The average research scientist in Readington, NJ earns between $63,000 and $134,000 annually. This compares to the national average research scientist range of $58,000 to $137,000.
$92,000
What is the job market like for research scientists in Readington, NJ?
You can compare the number of available jobs in Readington to the number of research scientist jobs in surrounding cities.
Active Research Scientist Jobs In Nearby Cities
| Nearby City | Jobs In Nearby City | Jobs in Readington | Difference |
|---|---|---|---|
| Bridgewater, NJ | 1,726 | 0 | -1,726 |
| East Brunswick, NJ | 3,265 | 0 | -3,265 |
| Easton, PA | 331 | 0 | -331 |
| Edison, NJ | 3,325 | 0 | -3,325 |
| Ewing, NJ | 1,695 | 0 | -1,695 |
What are the biggest employers of Research Scientists in Readington, NJ?
The biggest employers of Research Scientists in Readington, NJ are:
- Amneal Pharmaceuticals
- solaris
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