Senior Scientist Jobs in Readington, NJ

- 1,004 Jobs
  • Senior Clinical Scientist, Early Clinical Development - Hematology/Oncology & Cell Therapy

    But working at Bristol Myers Squibb is anything but usual. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
    $122k-147k yearly est.2d ago
  • Senior Scientist

    Immediate need for a talented Senior Scientist . This is a 12+ Months contract opportunity with long-term potential and is located in Summit, NJ(Hybrid). Please review the job description below and contact me ASAP if you are interested. Job ID:23-11290 Pay Range: $45 - $49/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location) . Key Responsibilities: Operate in a matrix team environment with collaboration with analytical development, global quality product leads, technical project teams, and regulatory groups etc. within Client. Support of commercial analytical change controls Support life cycle of regulatory filings, participates in preparation/reviewing of licensure applications, rest of world filings, follow-up measures, post-approval commitments and prior approval submissions Gathering, interpretation and presentation of data to support decision making Maintain effective partnerships with stakeholders from analytical development, Manufacturing Sciences and Technology, Supply Chain, Regulatory, Quality, Process Sciences, Drug Product Development, Project Management, and Manufacturing to deliver analytical strategies with a high probability of technical and regulatory success. Share expertise with matrix teams in support of analytical topics related to FDA, MMA, ROW & Client filing review. Support implementation of effective control strategy, analytical method and specification change control as needed throughout the Client network, third party manufacturing and outside testing labs. Serve as a subject matter expert for project, including technical evaluations of methods and data. Key Requirements and Technology Experience: Comprehensive knowledge and experience of analytical methodologies used for the development and commercialization of pharmaceutical products. Demonstrate a broad expertise and experience in analytics routinely used for in-process, release and stability testing of drug substance and drug product, product characterization and strategies to establish process and product knowledge. Extensive knowledge of the drug development process, analytical strategy and specification setting for drug substance and drug product Familiar with FAD, ICH guidance and major Pharmacopoeias. Working knowledge of CMC regulations and cGMP requirements, as well as experience in supporting regulatory filings and post approval changes. Strong communication and leadership skills in a highly interactive and fast paced environment. Experience in working with cross-functional strategic teams and collaboration with internal and external partners. A PhD, MS, or BS in Analytical Chemistry, Chemistry, or related disciplines with at least 1, 3, or 4 years of pharmaceutical industrial experience in relevant fields, respectively. This is primarily a analytical subject expertise and analytical project management role for a commercial program, including office work, teleconferencing, computer work, and running meetings, as well as working with quality control analysts in a laboratory setting requiring: Inside Work Working Alone Working with/around others Our client is a leading Pharmaceutical organization and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
    $45-49 hourly3d ago
  • Sr. 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 hourly4d ago
  • Sr. 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.9d ago
  • Engineering - 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 hourly25d ago
  • Scientist 2 - Research and Development (contract)

    Location: Raritan, NJ
    $79k-109k yearly est.8d ago
  • Staff Scientist

    Peak Environmental, A Nova Group, GBC Company
    $81k-122k yearly est.11d ago
  • Engineering - 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.23d ago
  • Associate 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.21d ago
  • Scientist Formulation

    Scientist to join the team.
    $81k-123k yearly est.17d ago
  • Urgent Need for Analytical Scientist @Contract to Hire

    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. Location : Warren, NJ
    $74k-108k yearly est.3d ago
  • Associate 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 yearly4d ago
  • Senior Engineering Scientist

    Contract Duration: 12 months + possibility of extension or FTE Pay: $42-50/HR Full Time/EOE Qualifications: PhD, MS, or BS in Analytical Chemistry, Chemistry, or related disciplines with at least 1, 3, or 4 years of pharmaceutical industrial experience in relevant fields, respectively Required to have pharmaceutical analytical experience with late phase and/or commercial phase of business. Comprehensive knowledge and experience of analytical methodologies used for the development and commercialization of pharmaceutical products A broad expertise and experience in analytics routinely used for in-process, release and stability testing of drug substance and drug product, product characterization and strategies to establish process and product knowledge Extensive knowledge of the drug development process, analytical strategy and specification setting for drug substance and drug product Experience with change controls, method validation and transfer, and some knowledge in regulatory filings, FDA and ICH guidance, and knowledge of Pharmacopoeia are highly valued Familiar with FAD, ICH guidance and major Pharmacopoeias Working knowledge of CMC regulations and cGMP requirements, as well as experience in supporting regulatory filings and post approval changes Experience in working with cross-functional strategic teams and collaboration with internal and external partners
    $42-50 hourly4d ago
  • Pharmaceutical 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.18d ago
  • Engineering - 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 hourly25d ago
  • Y - 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.8d ago
  • Scientist

    With expanding biologics pipeline, the Biologics Process Development organization within client & Co. is seeking a highly a motivated scientist to support testing and implementation of a cell culture media platform. Title: Upstream Processing Scientist - II (Associate) Location: Kenilworth, NJ
    $82k-117k yearly est.25d ago
  • R10520 Senior Scientist 1 Biologics - Chromatography & Separations Focus

    position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in
    $74k-111k yearly est.17d ago
  • Senior 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.4d ago
  • Translational 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.8d ago

Learn More About Senior Scientist Jobs

How much does a Senior Scientist earn in Readington, NJ?

The average senior scientist in Readington, NJ earns between $81,000 and $155,000 annually. This compares to the national average senior scientist range of $74,000 to $153,000.

$112,000

What is the job market like for senior scientists in Readington, NJ?

You can compare the number of available jobs in Readington to the number of senior scientist jobs in surrounding cities.

Active Senior Scientist Jobs In Nearby Cities

Nearby CityJobs In Nearby CityJobs in ReadingtonDifference
Bridgewater, NJ1,1620-1,162
East Brunswick, NJ1,9260-1,926
Easton, PA2490-249
Edison, NJ1,9540-1,954
Ewing, NJ9930-993

What are the biggest employers of Senior Scientists in Readington, NJ?

The biggest employers of Senior Scientists in Readington, NJ are:
  1. Johnson & Johnson
  2. Nestlé
  3. Nouryon
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