Regulatory Affairs Manager - Biotechnology
Monsanto - Saint Louis, MO
Title: Regulatory Affairs Manager - Biotechnology Location: North America-USA-Missouri-St. Louis Monsanto is seeking a highly motivate... individual to join The U.S. Biotechnology Regulatory Affairs Team as a Regulatory Affairs Manager. In this role, you will support the development...
Regulatory Affairs Manager - Biotechnology
Monsanto - Saint Louis, MO
Monsanto is seeking a highly motivate individual to join The U.S. Biotechnology Regulatory Affairs Team as a Regulatory Affairs Manager. In... to obtain and maintain U.S. and global regulatory approvals biotechnology-derived products across Monsanto's robust pipeline and business units...
Regulatory Affairs Manager - Biotechnology
Monsanto - Saint Louis, MO
North America-USA-Missouri-St. LouisDescriptionMonsanto is seeking a highly motivate individual to join The U.S. Biotechnology Regulatory... dossiers, agency submissions, and will lead efforts to obtain and maintain U.S. and global regulatory approvals biotechnology-derived products...
Regulatory Affairs Manager - Biotechnology
Monsanto - Saint Louis, MO
Monsanto is seeking a highly motivate individual to join The U.S. Biotechnology Regulatory Affairs Teamas a Regulatory Affairs Manager. In... to obtain and maintain U.S. and global regulatory approvals biotechnology-derived products across Monsantos robust pipeline and business units...
Regulatory Affairs Manager - Biotechnology
Monsanto - Saint Louis, MO
Monsanto is seeking a highly motivate individual to join The U.S. Biotechnology Regulatory Affairs Teamas a Regulatory Affairs Manager. In... to obtain and maintain U.S. and global regulatory approvals biotechnology-derived products across Monsantos robust pipeline and business units...
Monsanto - Saint Louis, MO
Provide key statistical support needed to demonstrate the efficacy and safety of Monsanto's biotechnology and chemical agricultural... products. 1. Provide experimental design and statistical analysis support in the area of regulatory sciences (environmental assessment , chemistry...
Monsanto - Saint Louis, MO
support in the area of regulatory sciences (environmental assessment , chemistry, and biotechnology). 2. Increase the level of statistical...Title: Statistician- Regulatory Location: North America-USA-Missouri-St. Louis Provide key statistical support needed to demonstrate the...
Sterling Life Sciences - Missouri
To apply, please use this link:http://www.mybiotechcareer.com/JD/RegulatoryAffairs-Job-Biotechnology-Missouri-10082or you can email resume... of global market clearances for multiple products4) Manage registration files, including required responses to regulatory agencies5) Provide...
Project Management Consultant, Life Sciences
Integrated Project Management - Saint Louis, MO
in the life sciences field, including pharmaceutical, biotechnology, and medical devices. The Project Management Consultant is a change agent... are a plus. Industry experience related to IPM's business offerings. 8+ years of experience in the pharmaceutical, biotechnology, and/or medical device...
Thought Leader Liaison, MS - St. Louis, MO
Genzyme Corporation - Saint Louis, MO
One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people... Accounts. Job Responsibilities: - Work within the Genzyme regulatory and legal compliance guidelines. - Act as Genzyme MS primary point...
Clinical Research Associate (CRA)
ICON Clinical Research - Saint Louis, MO
, biotechnology and medical device industries. We specialize In a highly fragmented industry, we are one of a small group of organizations with the... (i.e., identify investigators, help prepare regulatory submissions, conduct pre-study and initiation visits, etc.). Approximately 65-75% travel overall...
Aerotek - Kansas City, MO
Biotechnology company in the Kansas City area seeking qualified candidates for a QA Specialist position. Major Job duties include: -Providing support... for FDA, GMP, ISO, CE, and CSA regulatory programs. -Technical writing, process and departmental auditing, presentation of training, calling...
Project Progression Prophylactic Vaccines (Scientist/Sr
Pfizer Inc - Chesterfield, MO
candidate may also serve on project teams, assuming responsibility for delivering the analytical CMC strategy for regulatory submissions... against new technologies and evolving regulatory expectations. *Relocation assistance is available. Qualifications Educational Background: Minimum: BS...
Clinical Research Associate (CRA)
ICON Clinical Research - Kansas City, MO
, biotechnology and medical device industries. We specialize In a highly fragmented industry, we are one of a small group of organizations with the... (i.e., identify investigators, help prepare regulatory submissions, conduct pre-study and initiation visits, etc.). Approximately 65-75% travel overall...
Clinical Research Associates (CRA)
ICON Clinical Research - Kansas City, MO
, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical... regulatory submissions, conduct pre-study and initiation visits, etc.). Approximately 65-75% travel overall can be expected. In line...
Operating Procedures.Key Responsibilities:Write FDA and other country specific regulatory documents such as Clinical Protocols, Independent Review... research specific documentation that complies with GCPs and other regulatory requirements.Conduct research through various sources in order...
Project Progression Prophylactic Vaccines (Scientist/Sr
Pfizer Inc - Chesterfield, MO
candidate may also serve on project teams, assuming responsibility for delivering the analytical CMC strategy for regulatory submissions... against new technologies and evolving regulatory expectations. *Relocation assistance is available. Qualifications Educational Background: Minimum: BS...
Project Progression Prophylactic Vaccines (Scientist/Sr
Pfizer - Chesterfield, MO
, assuming responsibility for delivering the analytical CMC strategy for regulatory submissions and associated analytical aspects of vaccine... regulatory expectations. *Relocation assistance is available. Qualifications Educational Background: Minimum: BS/BA, MS, or PhD in pharmaceutical...
ICON Clinical Research - Missouri
years full time SAS programming experience in the pharmaceutical or biotechnology industry. - Familiarity with multiple software products... I through IV) and general regulatory requirements. - Demonstrated leadership skills as well as ability to work independently and on a team...
PharmaDiversity - Chesterfield, MO
also serve on project teams, assuming responsibility for delivering the analytical CMC strategy for regulatory submissions and associated analytical... and evolving regulatory expectations. *Relocation assistance is available. Qualifications Educational Background: Minimum: BS/BA, MS, or PhD in...