Job Description

• Perform routine operational support and Investigative tasks involved in the investigation of suspect samples (e.g., sample log-in, photographs, packaging variable data verification, packaging evaluations, physical appearance, etc.).

(NOTE: This position will only perform first person analysis)

• Perform non-routine sample analyses of suspect samples utilizing screening technologies.
• Produce quality documentation for internal and external use and ensure data documentation meets ALCOA plus expectations.
• Learn and utilize basic development, manufacturing, and regulatory processes, and develop an awareness of analytical and pharmaceutical industry trends related to product authentication.
• Work collaboratively with people in AQCO and with cross-functional business partners.
• Work safely and in compliance with applicable quality, environmental, and safety expectations. Ensure compliance with applicable Lilly global standards and regulatory guidelines.
• As needed within the AQCO organization, this position will help with shipping and purchasing needs

Qualifications

BS in the field of Chemistry, Biology, or a related field

• Fundamental knowledge of cGMP/GLP compliance requirements.
• 1-3 years of pharmaceutical experience.
• Capable of evaluating safety/quality compliance and supporting efforts to perform needed activities.
• Effective oral and written communication skills, self-management, task planning, and organization.
• Must be able to work productively in an interdisciplinary team environment.
• Ability to execute well-defined protocols/procedures with minimal oversight.
• Experience with basic analytical techniques (e.g., balances, pH meter, etc.).
• Theoretical experience with more sophisticated analytical techniques (e.g., microscopy, IR, NIR, Raman, HPLC, GC-MS, LC-MS, SEM-EDS), as required.
• Experience using IT tools such as: Veeva (QDocs), SmartLab, BLUE, NuGenesis, Empower, Tableau, CIMS, Trackwise, SAP, Fiori, etc.
• Experience with handling confidential/privileged information.

Additional Information

• The position is full-time, M- F 8 am to 5 pm
• May be requested to work on weekends, overtime, and holidays based on business needs.
• 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

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.