- Tris Pharma (Monmouth Junction, NJ)
- …in Monmouth Junction, New Jersey, Tris has an immediate opening for a Method Validation R&D Senior Scientist ISummary:The Method Validation (MV) Research and ... with company policies, SOPs, and state, federal and local laws Performs validation of analytical methods and release/stability testing for raw materials, IP, FP… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPrincipal Scientist - Mixed Modalities, Sterile Product DevelopmentThe Mixed Modalities team within Sterile Product Development is responsible for ... products.We are seeking a highly motivated candidate for the position of Principal Scientist (R5) focused on developing parenteral drug products across a range of… more
- Aequor (East Syracuse, NY)
- Job Title: Scientist , Analytical Sciences & TechnologyContract: 12 MonthsLocation: East Syracuse, NYJob ID: 1167QualificationsEducation / Experience / Licenses / ... 5% of domestic and/or international travel. ResponsibilitiesPosition SummaryThe Contractor Scientist within the Analytical Science and Technology team is responsible… more
- Tris Pharma (Monmouth Junction, NJ)
- Analytical Research and Development Scientist II Monmouth Junction, NJDepartment: Analytical Research and Development and Characterization / Analytical Development, ... has an immediate need for an experienced Analytical Research and Development Scientist IISummaryThe Analytical Research and Development (ARD) Scientist II, under… more
- Merck & Co. (South San Francisco, CA)
- Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for ... for assessment in large clinical populations.We are seeking a highly qualified physician- scientist with a proven track record in the pharmaceutical industry as well… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls(Associate Director Equivalent) Our company's Device ... with device design, requirement management, FMEA, design verification, design validation , statistical sampling, and control strategyExperience with regulatory fillingsWorking… more
- Merck & Co. (Rahway, NJ)
- …medical device engineering, particularly in the design, manufacturing, verification, validation and associated quality and regulatory aspects of combination ... of product design and development, manufacturing process development, qualification, validation , and design control and risk management techniques to positively… more
- Merck & Co. (Rahway, NJ)
- …Skills and Experience: Author analytical procedures, method development, validation and transfer protocols and reports, technical reports, experimental ... designs, and regulatory submission documents, etc.Perform investigations with strong technical troubleshooting skills and assist in developing/implementing CAPAs.Experienced in trace impurity quantitation, impurity isolation, and structure… more
- Merck & Co. (Rahway, NJ)
- …responsibility and leadership of internal and external work.The Senior Scientist , Engineering position leverages scientific/technical experience to develop safe and ... robust manufacturing processes through process characterization, technology transfer, validation , filing and supply support of late-stage projects in the small… more
- Merck & Co. (Rahway, NJ)
- …Company's Research & Development Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. The ... Principal Scientist is a senior scientific role tasked with working...using statistical software for design of experiments.Experience with qualification, validation , and transfer of assays to a GLP or… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist /Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a significant ... Conduct laboratory-scale and manufacturing-scale studies to support commercial process validation and characterization. You'll design experiments, analyze data, and… more
- BioAgilytix (Durham, NC)
- …need them.Our Liquid Chromatography/Mass Spectrometry (LC/MS) team is seeking a Scientist III to serve as Bioanalytical Project Manager (BPM)/Principal Investigator ... for someone with a strong background in method development, GxP-compliant validation , and targeted and untargeted analysis using chromatography and mass… more
- Merck & Co. (North Wales, PA)
- …lifecycle. Primary Activities :Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs ... and good programming practices.Maintain and manage a project plan including resource forecasting.-Coordinate the activities of a global programming team that includes outsource provider staff.Membership on departmental strategic initiative teams Education and… more
- Merck & Co. (North Wales, PA)
- Job Description Position Description This position is for a principal scientist in biostatistics.-The candidate should have a solid knowledge of statistical ... all programs meet analysis requirements, internal standard operating procedures, validation , and external regulatory requirements.6. Evaluates appropriateness of available… more
- Insmed Incorporated (San Diego, CA)
- …to keep you challenged and engaged. If you are a driven and astute scientist who is motivated to bring life-changing medicine to patients, then this is the ... specifications, protocols and author development reports.Demonstrated experience with process validation and scale-down models for biopharmaceutical processes, including interpretation… more
- Merck & Co. (Rahway, NJ)
- …Mechanical Testing, Medical Device Manufacturing, Medical Devices, Method Validation , Operational Acceptance Testing (OAT), Product Development, Prototyping, Social ... Collaboration, SolidWorks, Technical Writing-Preferred Skills:Job Posting End Date:09/5/2025 *A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE… more
- Merck & Co. (Rahway, NJ)
- …for statistical programming deliverables. Contribute to the development and validation of datasets following CDISC standards. Generate tables, listings, and ... graphics required for clinical trial decision-making, regulatory requests, clinical study reports, and new drug application filing. Produce SAS data transport files and program text files for regulatory submission. Assure high quality and timely deliverables.… more
- Merck & Co. (Rahway, NJ)
- …submission deliverables under the guidance of a senior level programmer.Perform validation tasks according to departmental SOPs and collaborate effectively with ... outsource partners.Act as a key collaborator with modelers, statisticians, and other project stakeholders to gather and document user requirements for statistical programming deliverables.Programmatically synthesize preclinical data into analysis ready… more
- BioAgilytix (San Diego, CA)
- …and metabolite profiling/ID. You'll guide a team of scientists through assay development, validation , and sample analysis under GxP, while also playing a key role in ... with clients to assure successful on time execution of assays, validation , and sample analysis under GxPs.Prioritizing tasks and managing schedules efficiently.Meet… more
- Insight Global (Upper Gwynedd, PA)
- Job Description Our Bio-pharmaceutical Client is seeking an Equipment Validation Scientist to join their team in West Point, PA. This individual will be a part ... validation , Change Control and testing documentation. The Equipment Validation Scientist will develop a suite of reporting, analytics and visualization… more
