Manager Purchasing - US / 08-5055 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Clinical QA Assurance Auditor / 08-5062 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Dep Director Product Mgmnt Associate US / 08-5084 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Manager RA / 08-5108 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Manager - Pharmaceutical Technology / 08-5145 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Manager, Case Management / 08-5147 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Manager R&D Quality Assuance Clinical Batch Release / 08-5166 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Manager, Logisitics and Warehousing / 08-5002 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Global Head, Clinical Outsourcing / 08-5139 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Direct Hire-Regulatory Affairs Manager |
| Kelly Scientific Resources is looking to fill a Direct placement position for an experienced R... |
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RA Manager- Pharma/Biologic
| Details |
Country: USA
Location: Pennsylvania-Allentown Allentown, PA
Total applied: 0 |
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RA Manager- Pharma/Biologic
PLEASE NOTE: To properly respond, you should format your resume in MS Word or Corel WordPerfect and send it to lar3919@jobquestsite.com . Visit our website at http://www.jobquestsite.com for other career opportunities. If your qualifications are not a perfect match- send your resume anyway. Opportunities for all levels of quality and regulatory as well as engineering and operations professionals available. IMPORTANT! No resume will be sent to Client without your consent. To be considered for this job you must have: BS in a Science field Must have a comprehensive knowledge of FDA regulations At least 3 years of product development regulatory affairs and experience in early phase regulation. Must be an excellent communicator. Preparation and submission of RA health submissions.DESCRIPTION: If you are tired of being a number with NO challenge in one of those “BIG” companies, Consider this Exciting JOB-New product development in the treatment of cancer and infectious disease, cutting edge technology, great advancement opportunity with well established, growing biopharmaceutical company. KEYWORDS: regulatory affairs, compliance, quality, FDA, 510k submissions, pharmaceuticals, biologics, biotechnology, antibiotics, Compensation: High: $105,000.00 plus Great Incentives & Relocation & BenefitsLow: $90,000.00 MRINetwork is the largest and most successful search organization in the world. Each MRINetwork office is a single point of contact to over 1,100 offices in more than 37 countries, our candidates have access to the right jobs virtually anywhere in the world. LOCATION: Allentown, PA JOB CATEGORY: Legal TYPE: Full Time, Employee JOB REFCODE: LAR3919 COMPANY: Management Recruiters of Myrtle Beach, Inc. CONTACT NAME: Lori Rowe, Account Executive EMAIL: Apply by Email
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