Associate - QA API EM

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.

We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Organization Overview:

Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The API EM Quality Assurance for Quality Control provides support to all QC activities at Contract Manufacturing organizations (CMs). The QA for QC position is essential for ensuring that all QC testing is in accordance with the validated methods and are compliant to cGMPs and regulatory commitments.

Key Objectives/Deliverables:

* Serve as a liaison between CMs and Lilly.

* Provide quality oversight of Quality control activities at CMs including being the initial point of contact for all quality-related issues with testing.

* Provide quality oversight of CM method validation or method transfer activities

* Escalate quality issues at CMs to Lilly QA management.

* Assist in the establishment and revisions of Quality Agreements with affiliates and customers.

* Ensure compliance to Quality Agreements and Manufacturing Responsibilities Documents (MRDs).

* Coordinate and perform quality responsibilities of API shipments for stability testing. Provide quality oversight of API EM stability program.

* Participate in regulatory inspection preparations with CMs.

* Ensure that documented checks have been completed for the Certificates of Testing and Certificates of Environmental Monitoring (where applicable), and deviations, changes and batch documentation that demonstrates requirements have been met prior to batch release.

* Provide quality support of Quality Control with the focus on holistic review of key activities associated with or impacting the quality control testing including deviations, change controls and countermeasures.

* Assess the impact of analytical deviation investigations and changes and ensure that all appropriate records are documented and retrievable.

* Maintain awareness of external regulatory agency findings which individually or collectively reference the quality of the product.

* Review and approve documents including, but not limited to, analytical procedures, change control proposals, deviations, analytical equipment qualifications, analytical methods and computerized system validations.

* Participate in APR activities.

* Participate in projects to improve productivity.

* Participate in Joint Process (JPT) and Post Launch Optimization (PLOT) Teams.

Basic Requirements:

* BS in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences.

* 5+ years of GMP Quality Control Laboratory knowledge and/or experience in API or finished product manufacturing, QA or Engineering.

* Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Preferences:

* Testing experience with Small Molecule

* Thorough technical understanding of quality systems and regulatory requirements relating to quality control laboratories

* Knowledge of pharmaceutical manufacturing operations.

* Demonstrated coaching and mentoring skills.

* Experience in root cause analysis.

* Demonstrated application of statistical skills.

* Demonstrated strong written and verbal communications skills.

* Strong attention to detail.

* Proficiency with computer system applications.

* Excellent interpersonal skills and networking skills.

* Ability to organize and prioritize multiple tasks.

* Ability to influence diverse groups and manage relationships.

Other Information:

* Must complete required training for API EM Quality Assurance.

* No certifications required.

* Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE.

* Must be able to support 24 hour/day operations.

* Up to 20% travel US & OUS.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form () for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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