Sr. Data Scientist- Consumer Deposits & Small Business
Sr. Data Scientist- Consumer Deposits & Small BusinessBoston, United States of America$105.1k-175k yearly1d ago
Research & Development Quality Technician - Food Industry
Backup The Research and Development Manager is the Backup when the Research and Development Technician is absent.$70k-104k yearly est.2d ago
Senior Clinical Scientist, Early Clinical Development - Hematology/Oncology & Cell Therapy
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. But working at Bristol Myers Squibb is anything but usual.$122k-147k yearly est.2d ago
Environmental Risk Assessment Scientist
Also, as an employee-owned firm, Kennedy Jenks offers a unique company culture with a corporate commitment to health, wealth, and self. Kennedy Jenks offers a comprehensive benefits package including medical, dental, vision, life and disability insurance, 401k, bonus opportunities, tuition reimbursement, professional registration support, a competitive PTO and holiday plan, and other benefits and programs. Kennedy Jenks offers a flexible hybrid working environment. Kennedy/Jenks Consultants, Inc. (Kennedy Jenks) provides engineering and scientific solutions for innovative water and environmental projects.$75k-90k yearly11d ago
Analytical Chemist
TSR is a premier National U.S. New Brunswick NJ Our client, a leading Pharmaceutical company is hiring an Analytical Chemist on a long term contract basis.$42-44 hourly4d ago
GCP Data Scientist / ML Engineer
Role: GCP Data Scientist / Client Engineer Location: Bridgewater, NJ$80k-114k yearly est.21d ago
Data Scientist - III
Job Posting Title: Senior Data Scientist We are looking for a Data Scientist to join our network data analytics experts' team to add value to our current data processes.$71k-101k yearly est.4d ago
Sr. Scientist Engineer Investigator
This is a 12 months contract opportunity with long-term potential and is located in Summit, NJ .$58-69.5 hourly21d ago
Scientist II
Our analytical team is currently seeking a Scientist II. We hope you will join us and become an advocate for diversity and inclusion here at Benjamin Moore. 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 Analytical Scientist II will develop and establish in-house analytical testing and characterization capabilities for coatings and raw materials. At Benjamin Moore, we believe diversity of culture, talent, and varying perspectives is key to a collaborative, innovative, and successful business. Benjamin Moore & Co., a Berkshire Hathaway company, is a leading manufacturer of innovative, high-quality coatings for the architectural and industrial maintenance markets. The Scientist II job is an exciting chance to join a team that promotes and recognizes innovation.$6k monthly10d ago
BI/Data Scientist - Exempt
Contributes to the effectiveness of security-related operations.
Provides programming support and assists in project planning for an operational area in information security.
Assists in daily oversight of a security sub-component.
Initiates projects intended to improve operations, client satisfaction with operational support, and development of appropriate standards and procedures for assigned operational area.
Participates in evaluation, testing and implementation of emerging control technologies, information systems security issues, safeguards, and techniques applicable to assigned operations area.
Presents proposed security enhancements to management for approval, funding and implementation.
Reviews and analyzes data and information to provide insights, conclusions and actionable recommendations.
Produces reports, analyzes, findings, etc.
Screens and selects tools to automate security administration.
Schedules and evaluates vendor security software through testing and discussions with external business users.
Contributes to the achievement of team objectives.
Bachelor's degree in computer science or a related discipline, or equivalent work experience required.
5-7 years of technology experience required; experience in the securities or financial services industry is a plus
RATE RANGE:
$55.00-60.00/hr. on w2 (negotiation expected)$55-60 hourly11d ago
Scientist 2 - Research and Development (contract)
Location: Raritan, NJ$79k-109k yearly est.8d ago
Engineering - Assistant/Associate Scientist
On-Board Scientific is hiring an Assistant/ Associate Scientist in Summit, NJ! 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 Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. 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. Job Location: Summit, NJ 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. www.onboardusa.com On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry.$41.9-43.2 hourly25d ago
CMC Scientist
Operate in a matrix team environment with collaboration with analytical development, global quality product leads, technical project teams, and regulatory groups etc.
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 and PAS filing review.
Support implementation of effective control strategy, analytical method and specification change control throughout the network, third party manufacturing and outside testing labs.
Serve as a subject matter expert for project, including technical evaluations of methods and data.
Provide critical analytical support for commercial change controls, RoW filing support, and commercial analytical activities.
Responsibilities include but are not limited to change control management, method review and summary, data verification, data summary and support for specification justification, reviewing dossier and related filing documents.
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
Ability to work in a highly matrixed environment, a quick learner and a team player.
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$77k-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
Analytical Chemist
A CRO company looking to hire an Analytical Chemist.$35-38 hourly2d ago
Engineering - 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.25d ago
Associate Director Clinical Research Scientist
Minimum of 8 years of experience in clinical research with at least 4 or more years of drug development experience A strong company culture commitment to their development they are actively seeking an Associate Director Clinical Research Associate.$73k-123k yearly est.4d ago
Research And Development Technician
Day-to-Day A CPG client in Florham Park is looking for an R&D technician to help start their production team.$84k-125k yearly est.4d ago
Data Scientist
We are seeking a highly motivated and innovative data scientist to join the data science and advanced analytics team within LDO until the end of 2023.$73k-103k yearly est.22d ago
Environmental Scientist
Maintains confidentiality; ensures that the firm is compliant with Federal and State laws and regulations. We are a progressive and growing environmental consulting firm with offices in Princeton, NJ, Buckingham Twp, and Bethlehem, PA. Our team is known for its development and successful implementation of cutting-edge and innovative projects and programs that advance our clients' interests sustainably into the future. Knowledge of the environmental regulatory framework.$50k-75k yearly est.4d ago
The average scientist in Readington, NJ earns between $65,000 and $133,000 annually. This compares to the national average scientist range of $67,000 to $140,000.
$93,000
What is the job market like for scientists in Readington, NJ?
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