The Technical Writer III is responsible for the development, creation, and revision of controlled documentation in accordance with policies and procedures, current GMP, 21CFR820, ISO 13485 and AATB Standards. Technical Writing in a GMP or medical device manufacturing environment. ...
In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical documents throughout the department. CMC Regulatory Technical Writer II. The technical writer contributes to various US, EU and rest of world (ROW) dossiers such as NDA, MAA, IND, IMPD, CTA...
Excellent technical writing skills and proficiency with Microsoft Word formatting functions; ability to efficiently create technically accurate documents for system lifecycle deliverables in alignment with the site validation program; highly attentive to spelling, grammar, punctation, and overall do...
Technical Writer – Pharma (Onsite, Warren, NJ). We are looking for a Technical Writer for our client, a Global Biopharmaceutical Company. Technical Writer – Pharma (Onsite, Warren, NJ). ...
Proven working experience in technical editing/writing skills in a wide variety of areas, specifically in writing materials such as Standard Operating Procedures, Work Instructions, User Guides, Software Release notes and documentation, and other system documentation as required. Ability to quickly ...
The CMC Regulatory Technical Writer II authors high quality Module and regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical documen...
The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical doc...
Job Title: Technical Writer and Document Analyst. Join our Cell Therapy Development Operations and Services team as a Technical Writer & Document Analyst. This role involves collaborating with various technical functions to meet submission deadlines and working closely with experts in Process Develo...
The CMC Regulatory Technical Writer II authors high quality Module and regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical documen...
APN Consulting has an immediate need for a direct client requirement: Job Title - Technical Writer Contract Duration - 3 Months Contract Location - Piscataway NJ 08854 HYBRID The Role We are seeking a detail oriented Technical Writer who can wr...
Technical manuals that describe the specific features of the data domain platform to ensure user ease of use. Writing be BRD’s related to the data domain project, creating high level technical ppt, and communicating with development and IT business partners. Technical Writing for IT in Bio-Pha...
Combo of DB testing + automation .DB Testing - ETL oracle testing .Automation: selenium, BDD, cucumber.Resource incentive comp experience - like Calidas (SAP), Varicent (IBM) - incentive comp tool (2 Years Experience)....
This could include user guides, technical API documentation, FAQs, system manuals, technical specifications, training materials, and more. Documentation: Collaborate with product owners, support specialists, trainers, and engineers to produce high-quality technical documentation for our products and...
As a Construction Inspector/ Project Manager on our Civil/Site Work team you will be responsible for providing project support and conducting on-site inspections to ensure compliance with project plans, specifications, and industry standards. We have an immediate opening for a Civil/Site Work Constr...
We are seeking a dynamic Technical Recruiter to join our growing team. As a Technical Recruiter, you will collaborate with hiring. Facilitates contacts by creating and maintaining a presence in the technical/industry. ...
The Senior Technical Project Manager is responsible for the overall management of Study Implementation Team members as assigned. The Senior Technical Project Manager oversees and analyzes the development trajectory of eCOA/ePRO technology within the portfolio to identify potential risks and mitigati...
Mentors and leads less experienced medical writers on complex projects, as necessary. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. We translate unique clinical, medical affairs a...
Mentors and leads less experienced medical writers on complex projects, as necessary. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. We translate unique clinical, medical affairs a...
Mentors and leads less experienced medical writers on complex projects, as necessary. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. We translate unique clinical, medical affairs a...
The managing editor is responsible for editorial direction, content, and tone of assigned journals in the managed care and population health vertical in both print and digital formats. Collaborate with the Assistant Editorial Director to develop and assign monthly editorial calendars. Ability to han...
The Project Manager II, Pipeline Integrity role is responsible for providing project management services for pipeline, station, and terminal projects throughout Buckeye. Buckeye Partners is currently seeking a Project Manager II, Pipeline Integrity with experience managing pipeline and/or terminal p...
As a Project Manager, you're responsible for NVR community homebuilding projects, ensuring high-quality home construction and on-time completion. ...
As we are rapidly expanding and have an opportunity for a Scientific Writer/Content Specialist to join our team in Princeton, New Jersey. Reporting to the Director of Content and Strategy, you'll develop the content for: (1) several different styles of training, primarily interactive media such as e...
Write advertising material for publications & internet media to promote children's special occasion dress sales; review advertising trends, consumer surveys, and other data to determine effective copy for product promotion.Req'd: BA any subject; knowledge of psychology; sales & marketing including ...
Sun Pharma Advanced Research Company (SPARC) is a pharmaceutical research and drug discovery organization that was formed in 2007 when SUN Pharmaceutical Industries Ltd separated out its active projects in drug discovery and innovation into a new company to provide the focus and the opportunity for ...