Author jobs in new jersey state USA
134 author jobs found in new jersey state: showing 81 - 100
Specialist, Quality Assurance External Operations
Company: Shiseido |
of all findings. Drive the Quality Vendor Compliance Manual training. Review, coordinate, and author SOP, WI, and forms to ensure...Location: East Windsor, NJ, USA
| Salary: unspecified | Date posted: 16 Jan 2025
Clinical Director, Oncology Early Development
Company: MSD |
: Author detailed development documents, presentations, budgets, and position papers for internal and external audiences...Location: Rahway, NJ, USA
| Salary: unspecified | Date posted: 15 Jan 2025
Process Expert
Company: Novartis |
as necessary. Deviations, Investigations, and CAPAs: Author investigations for product and non-product deviations. Conduct...Location: Morris Plains, NJ, USA
| Salary: $77000 - 143000 per year | Date posted: 15 Jan 2025
Manager, Quality Control Equipment
Company: Bristol-Myers Squibb |
: Serve as author or technical reviewer of appropriate departmental procedures. Review documentation...Location: New Jersey, USA
| Salary: unspecified | Date posted: 15 Jan 2025
Clinical Director, Oncology Early Development
Company: MSD |
: Author detailed development documents, presentations, budgets, and position papers for internal and external audiences...Location: Rahway, NJ, USA
| Salary: unspecified | Date posted: 15 Jan 2025
Expert Science And Technology - Gene Therapy Analytical Development - Chemistry
Company: Novartis |
challenges, communicate effectively and present complex data within the department and cross-functionally Author and/or review...Location: East Hanover, NJ, USA
| Salary: $93800 - 174200 per year | Date posted: 15 Jan 2025
Quality Assurance Shop Floor Lead
Company: Sanofi |
etc) Author significant and non-significant deviations, change controls, report etc. Present department KPIs...Location: Ridgefield, NJ, USA
| Salary: unspecified | Date posted: 14 Jan 2025
Quality Assurance Manager
Company: Sanofi |
, deviations Support Additional Quality functions (Media Fill Observer, Documentation Updates etc) Author significant and non...Location: Ridgefield, NJ, USA
| Salary: unspecified | Date posted: 14 Jan 2025
Specialist/sr. Specialist Data Integrity
Company: Bristol-Myers Squibb |
and author technical reports while effectively inputting and expressing Data Integrity principles. Completes routine tasks...Location: New Jersey, USA
| Salary: unspecified | Date posted: 12 Jan 2025
Sr Specialist It, Cell Therapy Manufacturing Systems
Company: Bristol-Myers Squibb |
, etc. Ability to author, review, and approve technical documentation, protocols, and reports, including IQ/IQ/PQ protocols, change controls...Location: New Jersey, USA
| Salary: unspecified | Date posted: 10 Jan 2025
Senior Principal Scientist, Clinical Research, Endometrial Cancer
Company: MSD |
of responsibility. To accomplish these goals, the Senior Director may: Author detailed development documents, presentations, budgets...Location: Rahway, NJ, USA
| Salary: unspecified | Date posted: 10 Jan 2025
Director, Toxicology Project Lead
Company: Insmed Incorporated |
, and interpretation of safety pharmacology and toxicology studies, ensuring high-quality, reliable data generation. Author and review...Location: Bridgewater, NJ, USA
| Salary: unspecified | Date posted: 09 Jan 2025
Ppg - Electrical Project Engineer
Company: QISG |
specific Client design reviews and coordination. Evaluate Client requirements and author clarifications and exceptions to RFPs...Location: Paramus, NJ, USA
| Salary: unspecified | Date posted: 09 Jan 2025
Data Analyst - Insurance - Remote
Company: Work at Home |
, Dynamics CRM, Dynamics GP, Share point, Excel, Power Query, Power Pivot. Ability to compile data results and author commentary...Location: Jersey City, NJ, USA
| Salary: $30 - 45 per hour | Date posted: 08 Jan 2025
Principal Medical Writer
Company: MMS Holdings |
protocol experience, as lead author, required Experience leading and managing teams while authoring regulatory documents..., and ICH guidelines a plus Substantial clinical study protocol experience, as lead author, required Experience leading and managing...Location: Jersey City, NJ, USA
| Salary: unspecified | Date posted: 08 Jan 2025
Regulatory Affairs Specialist
Company: Katalyst Healthcares & Life Sciences |
of regulatory CMC dossiers for new and existing commercial products. Work independently and effectively to manage and author... and lead the answer team of cross-functional SMEs to compile the responses in order to author and submit the responses timely...Location: Rahway, NJ, USA
| Salary: unspecified | Date posted: 05 Jan 2025
Director Regulatory Affairs
Company: TK-CHAIN LLC |
staff as required. Collaborates with functional groups to plan, author, compile and submit high-quality original...Location: Princeton, NJ, USA
| Salary: $90000 - 180000 per year | Date posted: 05 Jan 2025
Associate Director, Clinical Quality Compliance
Company: Pacira Pharmaceuticals, Inc. |
. Develop, author and revise departmental Standard Operating Procedures (SOPs) and serve as reviewer and approver of functional...Location: Parsippany, NJ, USA
| Salary: unspecified | Date posted: 04 Jan 2025
Senior Medical Writer (protocols) - Remote
Company: MMS Holdings |
.D. in scientific, medical, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience... a plus Substantial clinical study protocol experience, as lead author, required Experience leading and managing teams while authoring...Location: Jersey City, NJ, USA
| Salary: unspecified | Date posted: 04 Jan 2025
Computer System Validation Engineer
Company: TK-CHAIN LLC |
meet or exceed pre-defined quality standards. Author and execute Installation and Operational Qualification (IQ/OQ.... Author IQ/OQ protocols for new or used equipment purchased. Review IQ/OQ protocols provided by equipment manufacturers...