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| Job #03500 |
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| About our client |
| Our client is a small start up company. They are partnered with a pharmaceutical firm and are venture backed. They have money for the next two years. Great situation for someone who is entrepreneurial and wants to have a sense of accomplishment. |
| Position |
Location |
| Director Quality and Regulatory Affairs |
New Jersey |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Will write ANDA submissions for FDA approval. 2) Will implement a Quality Assurance System. |
| Requirements |
1) Must have strong understanding of Regulatory Affairs, especially ANDA or generic. 2) Must have implemented a Quality Assurance System.GMP. |

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