Trinity Health in the United States is seeking a CDI Specialist to improve the accuracy, clarity, and completeness of clinical documentation across inpatient, same-day surgery, observation, and emergency encounters.

You will perform concurrent medical record reviews, identify opportunities ...Read more

IQVIA Laboratories in Marietta, GA is seeking a Logistics Technician to support laboratory operations and ensure timely, accurate shipment of consignments. The role includes maintaining shipping docs, inventory, and compliance with Good Clinical Practice, with a 11:30 am–8 pm Monday–Friday sc ...Read more

Werfen is seeking a Senior R&D Technical Writer to prepare documentation supporting IVDR, FDA submissions, and regulatory filings for transfusion products. The role requires meticulous attention to detail, strong organizational and technical writing skills, and the ability to work across function ...Read more

Senior R&D Technical Writer - Transfusion

Country

United States

Shift

1st

About the Position

Introduction

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnost ...Read more

Introduction

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipm ...Read more

Werfen seeks a Sr. R&D Technical Writer to prepare technical documentation for IVDR and FDA submissions. You will work with Regulatory Affairs, Quality Control, Clinical Operations and Project Management to ensure compliant, precise documentation of products.

You will draft plans, protocols ...Read more

Overview

We are seeking a Sr. R & D Technical Writer who will be responsible for preparing technical documentation to support IVD design history files and regulatory submissions. Strong understanding of Quality Management Systems and Global IVD Regulations (including but not lim ...Read more

Centessa Pharmaceuticals seeks a Contract CMC Technical Writer to critically review data, methods, batch records, and development reports from external CDMOs to finalize source documents for analytical, drug substance and drug product, and to prepare regulatory content and summaries.

You wi ...Read more

Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is seeking a Contract CMC Technical Writer to critically review data, batch records, and development reports from external CDMOs to finalize source documents for analytical, drug substance and drug product.

The ro ...Read more