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Expense Analyst & System Maintenance |
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3 month temporary ... |
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Application Systems Support |
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Manager, Field Support (Oncology) |
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Sales & Marketing Analyst |
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Labeling Technician |
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Senior GMP Compliance Auditor |
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Senior System Validation Assoc. |
| Celgene is a multinational biopharmaceutical company committed to improving the lives of patients ... |
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Contract Clinical Study Manger - Devices |
| Job Description:
Our client is a leading medical device company in need of additional Clinical S... |
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IT Project Manager |
| IT PROJECT MANAGER
Barr Pharmaceuticals, Inc. a holding company, is a global specialty ... |
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Director of Quality
| Details |
Country: USA
Location: New Jersey-Northern Franklin, NJ 07416
Total applied: 37 Job Category:Quality Assurance/Safety
Relevant Work Experience:10+ to 15 Years
Education Level:Bachelor's Degree
Location:Franklin, NJ 07416
Status:Full Time, Employee
Occupations:Food Safety and Inspection;General/Other: Quality Assurance/Safety;Production Quality Assurance
Career Level:Executive (SVP, VP, Department Head, etc)
Relevant Work Experience:10+ to 15 Years
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Director of Quality
Director of Quality
NutriSport Pharmacal, Inc., a growing contract manufacturer of nutritional supplements located in northwestern, NJ has an immediate opening for an experienced Director of Quality. Responsibilities will include, but are not limited to: Overseeing the quality systems in the development, testing, manufacture, and packaging of nutritional supplements, while ensuring overall compliance to internal GMP procedures and external regulations. Manage, train, & support of all QA/QC department employees. Educate all employees on GMP systems requirements, compliance expectations, and help prepare company and serve as primary contact for all regulatory and client-related audits. Develop, originate, & revise SOP's, Master Batch Records, raw material and finished product specifications Thru the development & management of long-term & short-term regulatory strategic plans, provide leadership and technical expertise to identify needed improvements to current GMP systems, procedures, and practices to achieve full compliance with FDA.
The ideal candidate should have a background in nutritional/dietary supplements preferred, knowledge of industry regulations, GMP's and laboratory procedures. The candidate should possess strong problem solving skills with the ability to analyze data, effectively summarize findings, and draw conclusions. Must have strong communication skills with the ability to positively influence change at all levels of the organization. Manufacturing/R&D/laboratory background a plus. High level of knowledge of Part 111 for dietary supplements and other FDA-related regulations a plus. Potential employee should have a Bachelor's degree in related studies, advanced degree preferred, 10+ years QA/QC experience in related field. Our company offers a competitive salary with benefits including medical, dental and a company matching IRA. Please submit your resume with salary requirements for consideration. EOE
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