Batch updating translate

Seek continuous improvement of the quality of group’s deliverables and effective use of applicable technologies within the group and the Company.We are seeking a Quality Assurance Associate to be responsible for the Product Disposition function, encompassing the review of production batch records and associated documentation required to release a production lot.We are seeking a Quality Assurance Associate to be responsible for all QA-related aspects of material handling, storage, shipping and control, and associated documentation.This position may also be cross-trained on product disposition and regulated document/training functions.This position is the Head of Quality, with oversight for ensuring compliance with US and global regulatory requirements (e.g., FDA and EMA) and for site decisions affecting product quality and sustainable c GMP compliance and keeping Senior Management aware of critical issues within areas of purview.

We are seeking a Senior Pharmaceutical Manufacturing Technologist to be responsible for the manufacturing of clinical products in compliance with current Good Manufacturing Practice (c GMP) and Standard Operating Procedures (SOPs).

United States work visa sponsorship is not available for this position.

We can only consider your candidacy if you have authorization to work in the United States for any employer.

Salary will be commensurate with experience, plus a comprehensive benefit program United States work visa sponsorship is not available for this position. is not an E-Verify employer and cannot assist EAD holders in extending their OPT authorization.

We are seeking a Senior Biostatistician to provide statistical expertise and technical support as it relates to the design and statistical analysis of clinical oncology and autoimmune disease studies.

We are seeking a Director, Clinical Safety to be responsible for management and oversight of the clinical drug safety function associated with Company-sponsored and Investigator-sponsored clinical trials.

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