Author jobs in new jersey state USA
142 author jobs found in new jersey state: showing 1 - 20
Specialist, Planning & Scheduling
Company: MSD |
/processes to identify process improvements and ensure adherence to regulatory requirements. Author, review and approve SOPs... related to operational changes. Author and/or participate in investigations of atypical events and clinical complaints...Location: Rahway, NJ, USA
| Salary: $85600 - 134800 per year | Date posted: 31 Jan 2025
Lead Research Software Engineer
Company: Princeton University |
conduct experiments, analyze results, and co-author research publications. Develop, maintain, and improve our shared...Location: Princeton, NJ, USA
| Salary: unspecified | Date posted: 31 Jan 2025
Sr. Duck Creek Engineer
Company: Chubb |
Author/Server/Express 3.0 Rating, Forms, and Pages. Skilled in using Debugging Tools like Data Tester, Example Utility... on Example Author - Server, CBO express and Skins Strong ability to debug Duck Creek issues and provide solution for DC...Location: Whitehouse Station, NJ, USA
| Salary: unspecified | Date posted: 31 Jan 2025
Qms Manufacturing
Company: Pharma Universe |
. Collaborate with QA to ensure timely closure of QMS-related tasks. Author and revise batch records, SOPs, and forms...Location: Piscataway, NJ, USA
| Salary: unspecified | Date posted: 30 Jan 2025
Director, Quantitative Pharmacology, Pharmacometrics
Company: Penfield Search Partners |
. Responsibilities: Author/reviewer of clinical pharmacology and pharmacometrics submission documents and representative of the...Location: Princeton, NJ, USA
| Salary: unspecified | Date posted: 30 Jan 2025
Clinical Sas Programmer
Company: Katalyst Healthcares & Life Sciences |
implementation guides to independently author SDTM specifications from scratch; use Pinnacle 21 to run data conformance and create...Location: Bridgewater, NJ, USA
| Salary: unspecified | Date posted: 30 Jan 2025
Quality Manager
Company: Actalent |
. Responsibilities Serve as the appointed Management Representative. Lead, coordinate, author, and review regulatory filing documents..., and communication on quality initiatives. Conduct onsite audits and host regulatory agency audits as needed. Evaluate, author...Location: Emerson, NJ, USA
| Salary: $40 - 53 per hour | Date posted: 30 Jan 2025
Senior Expert Science & Technology, Analytical Development
Company: Novartis |
of quality and efficiency Author and review technical and regulatory documents to ensure completeness, accuracy, consistency...Location: East Hanover, NJ, USA
| Salary: unspecified | Date posted: 30 Jan 2025
Associate Copy Editor, Medical Education
Company: WebMD |
clarity, format, and flow (all while upholding the author's voice) Revising scientific language for usage, flow, and clarity...Location: Newark, NJ - Atlanta, GA, USA
| Salary: unspecified | Date posted: 30 Jan 2025
Senior Supplier Quality Specialist
Company: Bausch Health |
as required. Support Quality Metrics data collection and present the data in Quality Review Board Author and/or review of Quality...Location: Bridgewater, NJ, USA
| Salary: unspecified | Date posted: 30 Jan 2025
Human Factors Summer 2025 Intern
Company: Johnson & Johnson |
analyses, and Human Factors Engineering reports Author study documentation (e.g., informed consent forms, study participant...Location: Raritan, NJ, USA
| Salary: unspecified | Date posted: 29 Jan 2025
Manufacturing Manager - Bioservices
Company: Eli Lilly |
equipment is properly validated, and procedures are maintained within validated state Author and revise standard operating...Location: Branchburg, NJ, USA
| Salary: $104250 - 152900 per year | Date posted: 29 Jan 2025
Associate Principal Scientist – Device Technical And Engineering Lead (associate Director Equivalent)
Company: MSD |
strategy, timelines, milestones, and risks within our Company and with external suppliers Author and review relevant portions...Location: Rahway, NJ, USA
| Salary: unspecified | Date posted: 29 Jan 2025
Human Factors Summer 2025 Intern
Company: Johnson & Johnson |
analyses, and Human Factors Engineering reports Author study documentation (e.g., informed consent forms, study participant...Location: Raritan, NJ, USA
| Salary: unspecified | Date posted: 29 Jan 2025
Principal Scientist – Device Technical And Engineering Lead (director Equivalent)
Company: MSD |
, and risks within our Company and with external suppliers Author and review relevant portions of the regulatory submissions...Location: Rahway, NJ, USA
| Salary: unspecified | Date posted: 29 Jan 2025
Quality Management Systems Specialist
Company: Pharma Universe |
. Collaborate with QA to ensure timely closure of QMS-related tasks. Author and revise batch records, SOPs, and forms...Location: Piscataway, NJ, USA
| Salary: unspecified | Date posted: 28 Jan 2025
Manufacturing Qms
Company: Pharma Universe |
. Collaborate with QA to ensure timely closure of QMS-related tasks. Author and revise batch records, SOPs, and forms...Location: Piscataway, NJ, USA
| Salary: unspecified | Date posted: 28 Jan 2025
Manufacturing Quality Specialist
Company: Pharma Universe |
closure. Author batch records, SOPs and associated forms / formats required for manufacturing process. Responsible...Location: Piscataway, NJ, USA
| Salary: unspecified | Date posted: 28 Jan 2025
Therapeutic Data Strategy Director
Company: Novartis |
data, including vendor capabilities. Author the Clinical Data Section of Operational Execution Plan (OEP) (key customers...Location: East Hanover, NJ, USA
| Salary: unspecified | Date posted: 28 Jan 2025
Information Security Manager, Supply Chain Manufacturing
Company: Johnson & Johnson |
Life Cycle. Ability to learn quickly, employing different techniques as appropriate. Ability to independently author...