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Online Resumes with "cGMP "
Regulatory Pharmaceutical Document Specialist and Technical Writer
Brenda is a Technical Writer and Quality Assurance Regulatory Document Specialist with over ten years of experience in the pharmaceutical industry. She has extensive experience with all types of document project work, including writing, editing, formatting. She has experience as a team member for non-conformance investigations (NCs) and Corrective Action and Preventative Actions (CAPAs). Her analytical and research skil...
Sterile production Supervisor with extensive cGMP knowledge of Vaccines
Searching for a position that will allow me to show everyone the amount of drive I have to succeed and the patience I have dealing with people and troubleshooting. Honestly any position, but in theory one that I can remain in forever and advance.
Director, Chemical Process Development
Directed the groups responsible for development of safe, highest quality, and economical APIs under cGMP for pharmaceutical industry.
Tags for this Online Resume: Research & Development , Organic Chemistry in Pharmaceuticals , Scale-up, Piloting & Production, API, cGMP
Regulatory Affairs/cGMP Quality Assurance, Clinical Research industry & academic setting
Director Regulatory Affairs/QA cGMP academic setting or industry
Looking for a Project Manager, Project Engineer, Validation Engineer or Instrument/Control Engineer position.
* BS degree in Electrical Engineering & Computer Science with over 30 years of Controls Engineering experience * Over (10) years of SCADA Technology (coordinate SCADA project activities which include conceptual planning, design, development, installation, testing, and commissioning of SCADA related hardware and software systems; parties involved include vendors as well as internal customers, define requirements betw...
Tags for this Online Resume: Electrical Engineering, Project Engineer, Instruments & Control, Project Manager, IT Project Manager, Comissioning
QA Engineer, Columbus, OH
Engineering Professional with extensive experience in the medical device manufacturing industry. Expertise in managing and supporting Quality Assurance areas including design control, equipment qualification, process validation, process development, regulatory compliance and R&D activities. Proven abilities applied to Lean manufacturing, Six Sigma, cGMP, budget management, safety and ISO/FDA audits. Known for ability to ...
Tags for this Online Resume: engineer, lean manufacturing, quality
Quality Assurance Specialist - 10 years experience - FDA - cGMP
To partner with an established yet growing company where I can share my cGMP, FDA CFR Parts 210, 211 & 111 experience. Also my strong Quality Management Systems background and contribute to mutual growth.
