- Aequor (East Syracuse, NY)
- Job Title: Scientist , Analytical Sciences & Technology Contract: 12 Months Location: East Syracuse, NY Job ID: 1167 Qualifications Education / Experience / Licenses ... validating, and coordinating timely transfer of test methods with and to Quality Control laboratories is desired. Specific Knowledge, Skills, Abilities, etc. Strong… more
- Aequor (MA)
- Scientist Ocular Genomic Medicines, Genomics Medicine Unit We are seeking a laboratory facing Scientist to be part of a team focused on the development of Client ... IND enabling studies. Execute studies to generate proof of concept data . Apply expertise to design, develop scientific activities/projects to identify therapeutic… more
- Tris Pharma (Monmouth Junction, NJ)
- …Tris has an immediate opening for a Method Validation R&D Senior Scientist ISummary:The Method Validation (MV) Research and Development (R&D) Senior Scientist ... and advances required documentations, in liaison with Product Development (PD)/ Quality Assurance (QA)/ Quality Control (QC)/Regulatory Affairs, including… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Principal Scientist , Process Control and Data Analytics will be responsible for leading a team focused on developing and implementing product ... analysis, etc.Develop and implement statistical process control methodologies and data anlaysis to ensure the quality and...methodologies and data anlaysis to ensure the quality and reliability of autoinjector and syringe products, and… more
- Merck & Co. (Rahway, NJ)
- …Lead and oversee analytical investigations with a strong focus on quality and regulatory compliance.Excel in impurity isolation, unknown peak identification, ... integrity principlesCoach and mentor staff on analytical techniques, problem solving, and data integrity as needed.Share best practices across the company to enhance… 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 ... -The candidate will provide scientific expertise by learning and utilizing Quality Risk Management methodologies and tools for statistical design of experiments.… more
- Merck & Co. (North Wales, PA)
- …collaboration with Data Management/Programming.Collaborating cross-functionally to monitor clinical data to ensure quality , completeness, and integrity of ... execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and… more
- Merck & Co. (Rahway, NJ)
- …patients and global human health.Responsibilities: The Senior Statistical Programmer, Submission Data Standards Quality Management (SDS QM), provides oversight ... and quality management of submission data standard deliverables for world-wide regulatory application submissions of...tools and templates to support delivery focusing on traceability, quality assurance, data conformance and data… more
- Merck & Co. (Rahway, NJ)
- …Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (Rahway, NJ)
- …Methodologies (separation-based and residuals) and sound scientific understanding of Critical Quality Attributes/QbD/DOE principles as well as data analysis and ... Company's Research & Development Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. The… more
- Aequor (MA)
- As an experienced scientist , you will need to work independently and efficiently on Synthetic Biology including gene and oligo design, oligo synthesis, gene ... assembly, next generation sequencing and data analysis, nucleic acid purification and characterization, take lead in high throughput gene synthesis and plasmid… more
- Merck & Co. (Rahway, NJ)
- …collaboration with Data Management/Programming. Collaborating cross-functionally to monitor clinical data -to ensure quality , completeness , and integrity of ... of clinical protocol(s) . This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionGRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/Principal Scientist /Sr Principal ... pharmaceutical operations (eg, manufacturing, formulation and process development, analytical, quality assurance, n ovel modality and technologies such as synthetic… more
- Merck & Co. (Rahway, NJ)
- …to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .BPR&D within Research Laboratories is on a mission to rapidly deliver diverse ... and engage with the scientific community to influence the field.As a Principal Scientist you will have the opportunity to influence the future direction of Upstream… more
- Merck & Co. (North Wales, PA)
- …that project plans are executed efficiently with timely and high quality deliverables.For assigned projects the position serves as the statistical programming ... in developing analysis and reporting deliverables for R&D projects ( data , analyses, tables, graphics, listings)Strong project management skills; leadership at… more
- Insmed Incorporated (San Diego, CA)
- …deliver under pressure and time constraints, while maintaining a high level of work quality .Ability to present scientific data and concepts to CMC team members ... 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… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionResponsibilities:Provide high quality statistical programming deliverables for global stakeholders in Early Development Statistics and PK/PD Modeling ... oncology.Gather and interpret user requirements for programming requests, retrieve required data , transform data into analysis/modeling datasets, and develop… more
- Twist BioScience (South San Francisco, CA)
- …and storage solutions.Background in assay development, genomics-based diagnostics, or quality control for high-throughput NGS data .Software Development & ... Senior/ Staff Bioinformatics Production Scientist (Hybrid in South San Francisco)Position OverviewWe are seeking a highly motivated, results-oriented, and… more
- Merck & Co. (Rahway, NJ)
- … data analysis.Participates in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements.Collaborates ... Late Development Statistics. --Interacts with Clinical, Regulatory, Statistical Programming, Data Management and other company Research Laboratories Scientists in… more
- Merck & Co. (Rahway, NJ)
- …and biostatisticians and/or epidemiologists within BARDS, as well as stakeholders in data management, medical writing, and clinical operations to gather and document ... requests, clinical study reports, and new drug application filing. Produce SAS data transport files and program text files for regulatory submission. Assure high… more
