CV, Curriculum Vitae and Online Resumes Search
Recruiters - Try Postings!
Postings.com™ is a must-have for recruiters who want to:
- Find Qualified Candidates
- Find Job orders and Post Splits
- Be Found in Search Engines
- Implement a Social Sourcing Strategy
Job Seekers - Look Here!
Hitting a wall with your job search? Try Climber Premium.
- Top the Search Engines
- Unsurpassed Candidate Marketing
- Power Career Networking
- Fresh Jobs from the Net
Were you looking for Quality-Assurance-Regulatory job results?
Click Here to search for Quality-Assurance-Regulatory in our 2.4M jobs.
Online Resumes with "Quality Assurance Regulatory"
Biotech Quality Control Chemist Supervisor, Los Angeles County
A highly motivated, goal oriented professional with proven quality control/quality assurance/regulatory/research experience. Supervisory skills coupled with the ability to manage multiple projects and meet tight deadlines. Excellent technical abilities and a strong work ethic combined with excellent communication, organization, presentation and interpersonal skills.
Quality Control Laboratory Experience in Diagnostic, Pharmaceutical and Medical Devices Labs
I have worked consistently in QC for many years. As a result of my extensive background, my roles have increasingly crossed over into Quality Assurance and Regulatory Affairs. I want to advance into the realm of Compliance and Regulations.I feel I could be a valuable asset to any company that is regulated by GMP practices.
Tags for this Online Resume: CAPA, Quality Control, Documentation, Quality Assurance, Regulatory Affairs, Technical Writing
QA/Manufacturing Pharmaceutical Field
I have wide range of experience in the following - QA (in- process, finished products, raw materials, and documentation), large scale up & manufacturing process. Extensive experiences oversee activities and personnel in QA and Manufacturing. I am interested in any open position for supervision or above in Manufacturing, Quality Assurance, and Regulatory Affairs. I am willing to relocate for the right opportunity.
Tags for this Online Resume: QA/Pharmaceutical, Production/Pharmaceutical
Clincal Research Director; Medical Liason;Clinical Research Associate; Scientist
Hello, My Career goals and objectives are to find a good position within Pharmaceutical, Biotech, Medical Devices, Cosmetics, Government or private business that utilizes the wide array of skills, education and experience that I currently have to offer a company. Thank you! Annette M. Hormann
Tags for this Online Resume: Clinical Research Director, Clinical Research Associate, Medical Liasion, Scientist, Science Public Relations, Quality Assurance/Regulatory Affairs
Quality Assurance and Regulatory Affairs director
Tags for this Online Resume: Director Regulatory Affairs, Quality director
Admissions Director
quality assurance, regulatory officer
Quality Assurance/Regulatory Affairs/Compliance officer
Transform and maintain organizational performance in meeting FDA, CMS and Federal compliance.
Experienced Quality Professional, Medical Device - Northern NJ
Seeking an opportunity in Quality Assurance or Regulatory Compliance. Small and mid-sized companies offering variety and challenge are preferred, but will consider all full-time or consulting positions in the northern NJ/southern NY area that fit my experience.
Tags for this Online Resume: Quality System Documentation, Technical Writing, Regulatroy Compliance, Complaints MDR, Audit, Gap Analysis, Mentoring, Microsoft Office
Pharmaceutical, Clinical Research Quality Assurance and Regulatory Affairs
Transition more to clinical trial research than pharmaceutical operations. Challenging, fast paced, innovative company.
Quality, Regulatory Affairs, and Product Development Professional, Troy Ohio
Quality, R&D, and manufacturing executive with extensive experience in the coating and printing industries. Proven strengths in quality assurance, regulatory, business turnarounds, product innovation, strategic planning, and business development.
Tags for this Online Resume: quality manager, regulatory affairs, product development, ISO, audits, CAPA, FMEA, root cause
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...