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...
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...
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...
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...
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)....
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...
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). ...
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...
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...
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. ...
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...
We also work strategically with clients to create medical education for and outreach to healthcare professionals (HCPs) so they can make informed decisions in their practices. As we are rapidly expanding and have an opportunity for a Scientific Writer/Content Specialist to join our team in Princeton...
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 ...
As Project Manager, you are responsible for the successful execution of construction work. Is under the direct supervision of the Operations Manager, and is tasked with the successful completion of construction work in accordance with contractual obligations, internal policies and the Required Proje...
The Lead Content Writer is responsible for creation of written content, content organization, and content management for digital properties across both desktop and mobile applications. Key Roles and Responsibilities:With little to no supervision, writes, edits, and enhances content to meet establish...
As a Workday Student Project Manager, you will:. Create and manage to roadmaps, project plan, manage day to day monitoring tasks and activities, and initiate corrective action where necessary in order to keep the project on track. Successfully manage delivery of end to end Workday Student projects a...
You're an established Senior Medical Writer looking for the next challenge, or an experienced Medical Writer aiming to move up. Senior Medical Writers define new directions with CMC Affinity. IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, uni...
Clinical Communications, you will be working closely with an internal team dedicated to producing educational medical/scientific content (eg, peer-reviewed manuscripts, slide decks, video-based learning) for oncology care. You will have an opportunity to develop content on topics spanning the oncolo...
Responsibilities: Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias Write and edit clinical development d...