Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of...
AstraZeneca Pharmaceuticals LP
Job Description The role holder is responsible for ongoing management of quality performance, product disposition, regulatory compliance and oversight of quality issue resolution for commercial contract manufacturing organizations. Also responsible...
The Senior Manager/Associate Director, Clinical QA establishes and manages processes to control the quality of clinical studies conducted by Samumed. Responsibilities include ensuring adherence to the agency regulations, GxP, Industry Guidelines,...
Novo Nordisk, Inc.
Provide feedback to CRAs and their managers based on findings during on-site visits. Discuss visit outcome trends and findings with CRA Manager/Senior Director of Field Management and/or Director for CTM Quality to identify individual and department...
We are looking for a self-motivated looking for a Software and Configuration Management Engineer to design, build and maintain our global development infrastructure.
The right candidate for this position will be an experienced engineer who has...
Responsible for the management, implementation, and continuous improvement of the supplier quality management systems in compliance with CFR 820 and ISO13485 quality requirements and all other applicable standards.
This role provides...
Ultragenyx Pharmaceutical Inc.
Why Join Us?
Ultragenyx is a clinical stage biotechnology company committed to bringing to market novel products for the treatment of rare and ultra-rare diseases with an initial focus on serious debilitating metabolic genetic diseases. Founded in...
Strategic leadership role in ensuring establishment and maintenance of compliant, efficient internal GMP quality systems. Quality systems include, but are not limited to: Annual Product Review, Product Complaints, Vendor Management, Quality Metrics,...
Bulletproof Documentation, Inc.
The GMP Quality System Compliance Consultant will work with global quality system teams to restructure content of the corporate standards/policies and global procedures. validation documentation. The Consultant will provide global cGMP compliance...
This role will actively participate in product development and transfer activities, ensuring product and process conformance to FDA and ISO 13485 standards. This position will review validation methods and protocols, test methods, statistical...