The Role
Support pharmaceutical quality by managing deviations, preparing validation reports, performing qualifications, and leading investigations to ensure compliance in a highly regulated environment.
Summary Generated by Built In
The candidate should poses a BS in Science, Engineering, Physics, Biology, Chemistry or related fields.
It should have experienced working in the pharmaceutical industry, quality organization supporting deviations, validation reports, qualifications, investigations, at least 5 years of experience in a highly regulated environment.
Requirements
Doctorate OR Masters + 2 years of directly related experience OR
Bachelors + 4 years of directly related experience OR
Associates + 8 years of directly related experience OR
High school/GED + 10 years of directly related experience.
Skills Required
- Doctorate OR Masters + 2 years of directly related experience
- Bachelors + 4 years of directly related experience
- Associates + 8 years of directly related experience
- High school/GED + 10 years of directly related experience
- Experience working in the pharmaceutical industry quality organization supporting deviations, validation reports, qualifications, and investigations
- At least 5 years of experience in a highly regulated environment
- BS in Science, Engineering, Physics, Biology, Chemistry or related field (implied by description)
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The Company
What We Do
ISPV Inc. is a Life Science company that leads Productivity & Validation projects for the Pharmaceutical and Food industries.
