
Technician – Warehouse Quality Assurance
- Durham, NC
- Permanent
- Full-time
- Responsible for adhering to safety rules and maintaining a safe work environment for both you and others by supporting HSE corporate and site goals.
- Responsible for ensuring training is completed and remains in compliance.
- Ensures adherence and understanding of good documentation practices and compliance with applicable procedures for both Operations and Support personnel.
- Lead, mentor, and coach Operations, and support personnel on quality matters, while driving the site Quality culture.
- Ensures regular presence in warehouse and logistics areas to monitor GMP programs and quality systems.
- Reviews and approves GMP documentation in support of daily operations such as: Electronic Logs, and other documents as required
- Troubleshoot and provide QA systems support to reconcile issues in multiple systems (i.e., SAP, EWM, Darwin and other systems as required).
- Participate in self-led inspections and provide support during internal / external regulatory inspections.
- Ability to work cross functionally and work collaboratively with all levels of the organization. Work cross-functionally with the area process teams/flow team for metrics reviews, operational support, and issue / deviation management
- High School Diploma or equivalent
- Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
- Demonstrated decision making and problem-solving skills.
- Strong attention to detail.
- Proven ability to work independently or as part of a team to resolve issues.
- Ability to work overtime, as requested.
- Demonstrated strong oral and written communication and interpersonal skills.
- Demonstrated knowledge and understanding of manufacturing process and Quality Systems.
- Proficiency with inventory management systems and deviations systems, (i.e. SAP, Darwin, etc.)
- Previous work with combination products or devices with experience with US/EU regulations and notified bodies.
- Previous experience in GMP production environments.
- Previous facility or area start up experience.
- Knowledge of Validation / Qualification activities.