MAIN PURPOSE OF POSITION: Perform a wide variety of activities to ensure compliance with DURECT’s SOPs and applicable regulatory requirements MAIN DUTIES AND RESPONSIBILITIES: · Review manufacturing batch re...

To support the Nonclinical study activities by performing various aspects of nonclinical study and document management and GLP compliance. MAIN DUTIES AND RESPONSIBILITIES: · Assist with the placing, monitoring ...

Compliance Specialist Department: Legal Position Title: Compliance Specialist Reports to Manager’s Title: Associate General Counsel Location: Exton, PA FLSA Status: Exempt Full Time / Part Time: F...

The Head, Regulatory Affairs & Global Safety will oversee the strategic development of regulatory and global safety strategy and all supporting activities. These activities include management of all regulatory submissions to the FDA, oversight of staf...

Requires a Bachelors degree with a minimum of 8 years experience in the biotech/pharmaceutical industry. CPA and/or CFE certification strongly preferred. The qualified candidate must have 2 years of pharmaceutical fraud and abuse experience along...

The Quality Assurance Associate’s primary responsibility will be to support Isis’ quality systems as they relate to the manufacturing and testing of Drug Substance (DS) and Drug Products (DP). Principal duties include, but are not limited to: ...

Job Reference Code: AFF-801 Job Title: DIRECTOR OF QUALITY ASSURANCE Location: Upper Midwest Salary: $150K + Bonus We are seeking a seasoned QA executive with managerial skills to lead a large quality organization for a leading parenteral drug ...

Job Title: Quality Assurance Manager Location: Southeastern US Salary: $120K + Bonus Broad-based QA position that will oversee a variety of compliance-related activities for a very large pharmaceutical company. This division operates as a virtual ...

Job Title: SENIOR DIRECTOR QUALITY ASSURANCE Location: West Coast Salary: $250,000 + Bonus/Stock Major Pharma company headquarted in California seeks their top manufacturing QA executive who will oversee all aspects of compliance to include docume...

Will manage the entire QA/compliance effort for a growing pharmaceutical firm located in an attractive Florida city. Duties will include oversite of compliance, documentation, FDA interface, change controls, validation, etc. Visible position with signif...

Seeking a Quality Assurance Associate to perform QA Packaging and Process Improvement activities. Duties and Responsibilities Perform QA Packaging Activities a. Perform batch record review b. Perform deviation in...

OSI Pharmaceuticals is committed to “shaping medicines and changing lives” by discovering, developing and commercializing high-quality and novel pharmaceutical products that extend life or improve the quality of life for patients with cancer, ...

OSI Pharmaceuticals is committed to “shaping medicines and changing lives” by discovering, developing and commercializing high-quality and novel pharmaceutical products that extend life or improve the quality of life for patients with cancer, ...

OSI Pharmaceuticals is committed to “shaping medicines and changing lives” by discovering, developing and commercializing high-quality and novel pharmaceutical products that extend life or improve the quality of life for patients with cancer, ...

OSI Pharmaceuticals is committed to “shaping medicines and changing lives” by discovering, developing and commercializing high-quality and novel pharmaceutical products that extend life or improve the quality of life for patients with cancer, ...