This position is expected to be between 12 to 17 weeks on a 40-hour week basis. Actual work schedule can be negotiable. However, initial involvement in April through 3rd week of May needs to be near full time.
MacroGenics, Inc., a growing biotechnology company, has an opening for a Validation Specialist in its Rockville facility. Responsibilities include: validating temperature controlled equipment, process equipment, utilities,...
The Manager, Document Control has overall responsibility for developing, implementing, managing and the Document Control Systems according to FDA GxP requirements, ICH GxP requirements, internal and typical pharmaceutical industry practices.
The Associate Director, QA Lot Disposition is responsible for directing the quality activities required to accurately complete the review and approval of the Raptor QA document and record review for drug substance and commercial and clinical drug...
BioSpace Career Fairs
BioCapital Career Fair
Hyatt Regency Bethesda
Thursday, May 6, 2014
1- 6 p.m.
Spend a day with HR reps and Hiring Managers from top biotech, pharma, medical device and diagnostics companies.
Companies recruit for roles in...
FibroGen seeks a Quality Assurance Senior Manager/Associate Director to support the manufacture of Drug Substance and Drug Product at Contract Manufacturing Organizations (CMO) and Contract Research Organizations (CRO) to ensure FibroGen products are...
Job Title: Director, Quality Assurance
Reports To: President R&D, Chief Scientific Officer
FLSA Status: Exempt
The Director, Quality Assurance has overall responsibility for Quality Systems management within...
Lab Support, A Division Of On Assignment
South San Francisco,
Perform Quality Assurance review/approval of validation documentation to ensure compliance with stated requirements, company standards, regulatory expectations and industry standards
Serve as the Business Quality representative on cross-functional...
Cubist Pharmaceuticals, Inc.
The Senior Manager/Manager plays a pivotal role in the Clinical QA and Compliance function within the Clinical Operations department by serving as a GCP compliance expert to the Cubist clinical development organization. The Senior...
Performs internal and external GMP and Quality System audits and ensures follow up on audit observations. Maintains audit schedule and ensures audits are performed when planned. Provides metrics to management regarding compliance of audited...