Employee Responsibilities:
- Complete data integrity review of analytical data reporting records for the client’s portfolio, which includes Synthetic molecules, Peptides, and Bioproducts
- Support development stability studies which include handling, storing, delivering samples, and documenting per relevant procedures
- Assist domestic and international shipping of material, such as development samples or consumables
- Must be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements
The Ideal Candidate would possess:
- Strong computer and organizational skills
- Excellent communication (oral and written) and attention to detail
- Ability to work independently and as part of a team, and have self-motivation, adaptability, and a positive attitude
- Ability to learn complex processes and procedures, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies
Minimum Qualifications:
- Bachelor's degree in Science or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
- Authorization to work in the United States indefinitely without restriction or sponsorship
- 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
- #LI-EB1
- Authorization to work in the United States indefinitely without restriction or sponsorship
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
