- ThermoFisher Scientific (Middleton, WI)
- …Practices (GMP) Safety Standards, Office **Job Description** At Thermo Fisher Scientific , you'll discover meaningful work that makes a positive impact on ... Impactful Work:** Assists in the coordination and preparation of basic scientific documents under direct supervision. Responsible for preparing and editing … more
- Takeda Pharmaceuticals (Madison, WI)
- …life-changing therapies to patients worldwide. Join Takeda as a Principal Medical Writer where you will working across therapeutic areas to provide expert support ... the Medical Writing team, you will report to the Associate Director. **How you will contribute:** + Reporting to...to a Medical Writing Team Lead, the Principal Medical Writer guides medical writing activities for key clinical and… more
- Catalent Pharma Solutions (Madison, WI)
- **Position Summary** ** Associate Lead I - Biomanufacturing, Technical Writing** Catalent is a global, high-growth, public company and a leading partner for the ... manufacturing in accordance with regulatory, site, and client requirements. The Associate Lead I - Biomanufacturing, Technical Writing under minimal supervision,… more
- Takeda Pharmaceuticals (Madison, WI)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as a Associate Director Medical Writing where you will be responsible for medical writing ... presentation and interpretation. In addition to project responsibilities, the Associate Director, Medical Writing is responsible for non-project related activities… more
- Takeda Pharmaceuticals (Madison, WI)
- …the best of my knowledge. **Job Description** **About the role:** ** Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology and ... will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department within… more