Get Our FREE Industry eNewsletter


Refine Job Search:

Clear All Selections
Selected Area of Expertise
Compliance

Clear All Selections

Your search returned 8 jobs



7/29/2014
Intertek Group PLC
San Diego, CA

The Scientific Director is responsible for activities related to the development and validation of immunoassays in accordance with relevant regulatory requirements including Good Laboratory Practices (GLPs). This individual will also interact with...

7/24/2014
Mega Aid Compounding Pharmacy
Brooklyn, NY

The ideal candidate for our growing Pharmacy will possess an extensive knowledge of drug resources and have senior level experience as a Pharmacist that has managed laboratory and/or manufacturing set up. We are looking for someone that has at least...

7/16/2014
Bavarian Nordic
Mountain View, CA

Primary Responsibilities: Manages/organizes all lab operations and supports tasks pertaining to company research and development activities. Specific responsibilities include: • Oversee facility activities to monitor compliance to regulations,...

7/14/2014
SciGenium
Cambridge, MA

Document Security Administrator Location: Cambridge MA We are currently looking for an individual who can play a key role in the configuration, implementation, and ongoing oversight and management of an electronic document management system. This...

7/11/2014
SAFC Carlsbad
Carlsbad, CA

• Compliance with safety guidelines • May perform lot file review, which will include batch records and associated documentation Identify documentation and procedural errors Communicate errors noted to operations staff Notify client of deviations...

7/11/2014
SAFC Carlsbad
Carlsbad, CA

ESSENTIAL JOB FUNCTIONS • Act as a trusted and valuable resource of technical expert in Bioassay • Oversee day-to-day operation of Molecular & Cell Biology Team •Direct and/or drive assay development/ assay transfer and/or assay validation...

7/9/2014
KARL STORZ Endoscopy-America, Inc.
El Segundo, CA

Timely handling of the increasing volume and complexity of contract-related work is unsustainable and has already placed a drag on deal execution and could constrain growth where contracts are involved. This person would report to Jenny Smyth, the...

7/1/2014
Clovis Oncology
San Francisco, CA or Cambridge, UK, CA

Roles and Responsibilities: • Manage the clinical quality assurance program, which includes the development and execution of quality plans for each study, as well as auditing of investigator sites, vendors, databases and clinical study reports. •...