Senior GMP Auditor - Sparta, NJ

We are seeking a highly experienced Senior GMP Auditor with deep expertise in pharmaceutical manufacturing and clinical packaging operations. · This role will perform a comprehensive, independent audit of a CDMO manufacturing and clinical packaging facility located in the United ...

This is a remote role with occasional travel to our clients' sites across the US. Our organization is seeking a highly experienced Senior GMP Auditor with deep expertise in pharmaceutical manufacturing and clinical packaging operations. · Key Responsibilities · Plan, lead, and ex ...

The RPT QA Auditor is responsible for planning conducting and reporting on internal and external audits to ensure compliance with cGMP regulatory requirements and company quality standards. This role supports the Pharmaceutical Quality System PQS by identifying gaps recommending ...

Harrow is an entrepreneurial company where every member of the team can be their own CEO. They value innovation and patient access to affordable medicines. As a Front Office Coordinator, you will manage front desk activities and ensure a professional environment for employees, vi ...

Sr. Auditor needs experience in Radio Pharmaceuticals and auditing. · Conduct routine audits of internal processes and suppliers. · Ensure adherence to regulatory guidelines. · ...

At Daiichi Sankyo we are united by a single purpose to improve lives around the world through innovative medicines. · We have a legacy of innovation since 1899 and are advancing breakthrough therapies in oncology cardiovascular disease rare diseases and immune disorders. · ...

Accountable to organize and directs an audit universe for GMP relevant activities involving but not limited to supplier qualification program clinical/IMP vendor audits. · ...

We are united by a single purpose to improve lives around the world through innovative medicines. We are advancing breakthrough therapies in oncology cardiovascular disease rare diseases and immune disorders. · ...

The RPT QA Auditor is responsible for planning conducting reporting on internal external audits ensure compliance with cGMP regulatory requirements company quality standards. · This role supports the Pharmaceutical Quality System PQS by identifying gaps recommending corrective ac ...

The RPT QA Auditor is responsible for planning conducting and reporting on internal and external audits to ensure compliance with cGMP regulatory requirements and company quality standards This role supports the Pharmaceutical Quality System PQS by identifying gaps recommending c ...

The Director of Quality Assurance provides strategic leadership to ensure the highest standards of quality, · compliance, · and operational excellence across company's manufacturing,supply chain,and product development operations worldwide.This role owns the global Quality Manage ...

The Manager, Quality Assurance Compliance is a key member of the Quality organization responsible for ensuring that all operations comply with applicable US FDA and EU GMP requirements. This role supports regulatory compliance internal audit supplier qualification programs ensuri ...

Serving as a QA head, the Associate Director Quality Assurance provides strategic leadership and direction to the site's Quality Assurance function, ensuring the highest standards of cGMP compliance, product quality, and data integrity across solid orals, · sterile/aseptic manufa ...

Provides management of Compliance activities for the site following Innovation Labs policies standards procedures and cGMPs This will include USA & Canadian regulatory compliance to the FDA and Health Canada regulations. The job includes organization and maintaining documentation ...

We are seeking an experienced Senior QA Auditor with a strong background in Radiopharmaceuticals (RPT) to join our quality assurance team.This role plays a critical part in ensuring compliance with cGMP, GDP, FDA, EMA and ICH regulatory standards while supporting the Pharmaceutic ...

At Par Health we believe great healthcare is built on getting the essentials right. · We re looking for passionate talented individuals who share our commitment to improving lives.. · Elevating the Essentials isn t just our tagline it s the higher standard we live by every day.Th ...

Weiss-Aug is a leading provider of advanced manufacturing and engineering solutions with advanced facilities across the U.S. and Mexico for over 50 years.As a recognized leader in the industrial and commercial sectors, · specializing in high-volume metal stamping, · thermoplastic ...

The Director of Quality Assurance provides strategic leadership to ensure the highest standards of quality compliance and operational excellence across company manufacturing supply chain and product development operations worldwide This role owns the global Quality Management Sys ...

The Manager, Quality Assurance Compliance is a key member of the Quality organization, · responsible for ensuring that all operations (Solid Orals as well as sterile manufacturing and aseptic filling operations), systems, and suppliers supporting the CDMO site comply with applica ...

We are seeking a detail-oriented Quality Assurance Specialist to join our team. · ...