Stability / Reference Standard Specialist at Eurofins — Indianapolis, IN
Full-timeIndianapolis, INPosted 2026-07-22Apply on SmartRecruiters
Full job description
- Build and maintain stability studies in Lab Information Management System (LIMS)
- Manage label request program
- Manage inventory system
- Receive, store, forecast, submit, and deliver stability and analytical samples
- Understands and follows all relevant policies relating to this job including business, compliance, quality, environmental and safety expectations
- Supports the development, registration and launch of new pharmaceutical products
- Support the client's work requests as needed
- Support domestic and international shipping of material
- Additional duties as needed
The Ideal Candidate would possess:
- Fundamental knowledge of cGMP compliance requirements
- Excellent communication (oral and written) and attention to detail
- Strong computer and organizational skills and experience with Microsoft Office
- Ability to work independently and as part of a team, have self-motivation, adaptability, and a positive attitude
- Ability to learn new techniques, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies
- Must be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements
Minimum Qualifications:
- Bachelor's degree
- 2 years professional experience
- Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.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