Qualifications
** Minimum Qualifications:**
- Bachelor’s Degree in a science discipline (chemistry, biology, biochemistry, or related scientific discipline).
- Three to five years in research and development or formulation role focused on large molecule/biologics drug substance/product development.
- Pharmaceutical industry experience in CMC technical drug development (drug substance and/or drug product experience in analytical development or formulation).
Preferred but Optional:
- Three or more years of direct global regulatory CMC experience, or equivalent experience supporting CMC functions contributing to clinical trial phases of development in various regions, including US, EU, and Asia.
Additional Information
- Position is full-time, working Monday-Friday 8:00 a.m.-5:00 p.m, overtime as needed
- Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply.
- Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
- Authorization to work in the United States indefinitely without restriction or sponsorship
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Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.