Intern- CMC - Paramus

· SUMMARY: · A Pharmaceutical CMC (Chemistry, Manufacturing, and Controls) Writer plays a crucial role in regulatory submissions by preparing technical documents related to drug development, manufacturing, and quality control. · JOB DESCRIPTION: · Authors a range of clinical doc ...

· CMC Writer, Chemistry, Manufacturing, and Controls, Regulatory, Drug Development, Manufacturing, and Quality Control, NDA/MAA CTD, EU (IMPD and MAA), US-FDA, FDA, · If you post this job on a job board, please do not use company name or salary. Experience level: Mid-senior Educ ...

· SUMMARY OF POSITION: · Assist and support the Associate Director in managing Contract Development and Research Organizations (CDMO) in the areas of Clinical Supplies. · Review master batch records (MBR), Master Packaging Work Orders (MPWO), and clinical related supplies-relate ...

· Clinical Supplies Manager needs Bachelors degree in chemistry (preferred analytical) and up to 5-8 years of experience working in an analytical laboratory background · Clinical Supplies Manager requires: · CDMO management, Master Batch Records (MBR), Master Packaging Work Ord ...

· Clinical Supplies Manager Paramus, NJ · Clinical Supplies Manager Paramus, NJ · Experience level: Mid-senior · Experience required: 8 Years · Education level: Bachelors degree · Job function: Management · Industry: Pharmaceuticals · Pay rate : View hourly payrate · Total posit ...

The Clinical Supply Manager is responsible for the end-to-end strategic planning and operational execution of clinical trial material CTM supply chains. · This role leads the management of global Contract Development and Manufacturing Organizations CDMOs to ensure the timely pack ...

The Clinical Supply Chain Manager is responsible for the end-to-end strategic planning and operational execution of clinical trial material (CTM) supply chains. · A key focus of this position is the oversight of Interactive Response Technology (IRT) systems. · ...

+The Clinical Supply Manager oversees end-to-end strategic planning of clinical trial material supply chains. · +Aggregate future requirements into a comprehensive supply/demand forecast. · Collaborate with Clinical Operations to align supply forecasts. · ...

We are seeking a Senior National Account Manager to join our team in Totowa US. As a global leader in smart buildings Johnson Controls empowers you to build your best future Our teams are strategically positioned to support industries across the globe You will have the opportunit ...

· Boehringer Ingelheim is currently seeking a talented and innovative co-op to join our CMC Regulatory Affairs department located at our Ridgefield facility. In this role you will perform regulatory submissions to US NDAs and BLAs and improve compliance tracking of marketed prod ...

Boehringer Ingelheim is currently seeking a talented and innovative co-op to join our CMC Regulatory Affairs department located at our Ridgefield facility. In this role you will perform regulatory submissions to US NDAs and BLAs and improve compliance tracking of marketed product ...

Advance your career with Johnson Controls team as Senior National Account Manager for Security role. · ...

Join a Team Where Your Work Truly Makes a Difference · Safe Children, Stable Families, Successful Lives. · At CMCS (Cardinal McCloskey Community Services), our mission is to protect, empower and promote independence for at-risk Children & Families and those with developmental dis ...

Join a Team Where Your Work Truly Makes a Difference · Safe Children, Stable Families, Successful Lives. · At CMCS (Cardinal McCloskey Community Services), our mission is to protect, empower and promote independence for at-risk children and families and those with developmental d ...

Join a Team Where Your Work Truly Makes a Difference · Safe Children, Stable Families, Successful Lives. · At CMCS (Cardinal McCloskey Community Services), our mission is to protect, empower and promote independence for at-risk children and families and those with developmental d ...

The mission of HUTCHMED International Regulatory Affairs is to develop innovative global registration strategies that advance our pipeline through approval in US, EU, and other countries. · Lead CMC regulatory strategy development and implementation that incorporates risk identif ...

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, ...

The Associate Director is responsible for regulatory CMC activities from early development to post-approval phase. · Organize and manage the preparation of submissions to Health Authorities. · Coodinate activites required for timely and accurate reporting of information to existi ...

This position will coordinate activities with all functional departments in support of regulatory filings. Manage assigned projects to ensure thoroughness, accuracy, and timeliness of CMC dossiers and responses. · ...

(Senior) Director, CMC QA – Permanent – New York · Proclinical is seeking a (Senior) Director, CMC Quality Assurance for an emerging biotech company based in New York. · Primary Responsibilities: · In this role, you will be responsible for the hands-on oversight of all Quality A ...