Stability Reference Standard Specialist

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 Qualifications: Qualifications 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 Additional Information 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

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Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. Compensation: $24-$24 #J-18808-Ljbffr Eurofins USA PSS Insourcing Solutions