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.
The Quality Assurance Floor Support Team assures patients worldwide of safe and efficacious drug products, through effective quality oversight of Indianapolis Parenteral Operations activities.
The QA Floor Lead Tech is responsible for providing daily support and oversight to GMP operations in Raleigh-Durham North Carolina. The QA Floor Support Lead Tech works as a team member supporting multiple production functions (formulation, filling, and visual inspection), from operations to maintenance, to achieve site goals while providing Quality oversight and guidance.
Responsibilities:
Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals
Provides daily presence in operational areas to:
monitor GMP programs and quality systems and ensure adherence and understanding of good documentation practices and compliance with applicable procedures for both Operations and Support personnel.
monitors for, retrieves, and completes review of all paperwork in need of quality review in each area supported and coordinates delivery to the associated area when complete.
Supports visual inspection AQL inspection.
Review and approve GMP documentation in support of daily operations such as:
Cycle Summary Reports for equipment
Electronic batch record initiation
Daily documentation of quality on the floor oversight
Maintenance action plans
Return to Service and Release of equipment, product, and area HOLDs
Work Order assessments and issue resolution
Other documents as required
Provide guidance and assistance in identifying potential product quality impact and assessing if Observations are required
Performs observational requirements for Aseptic Process Simulation 14-Day Reads and supporting observation during formulation and fill related aseptic activities.
Provide QA systems support to reconcile issues in multiple systems such as:
SAP (inventory management)
PMX (electronic batch record)
TrackWise (compliance
Veeva (controlled document repository)
GMARS (calibration and maintenance system)
And other systems as required
Work within team to ensure all manufacturing areas receive QA support needed to maintain daily operations
Reviews GMP documents (e.g., Procedures, Protocols, and Production Record Instructions)
Basic Requirements:
High school diploma or equivalent
Demonstrated relevant pharmaceutical experience in aseptic manufacturing
Additional Preferences:
Associates degree in a science, engineering, computer, or pharmaceutical related field of study, preferred
Strong oral and written communication and interpersonal skills
Strong attention to detail
Experience in Production QA, QC is desirable
Experience in Visual Inspection is desirable
Experience with TrackWise Deviation and Change Management processes
Additional Information:
This position will support a 24/7 operation, working a rotating twelve (12) hour day shift schedule. During the project and onboarding phase, role will work eight (8) hours Monday-Friday day shift, then transition to the rotating twelve (12) hour day shift stated above upon approval from Supervision/Management.
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.
Completion of Post Offer Exam or Completion of Work Simulation if applicable
Maintain qualifications and certifications for access to all supported areas required of the position.
Mandatory overtime may be required, planned and unplanned.
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 (https://careers.lilly.com/us/en/workplace-accommodation) 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.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$28.12 - $51.68Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.
At Lilly, we’re on a mission to enhance lives through discovery and patient care, and we’re thrilled to announce that we’re looking for a Lead QA Tech - Parenteral to join our Quality Assurance Floor Support Team in Research Triangle Park, NC. In this vital role, you’ll provide critical oversight of GMP operations in the vibrant Raleigh-Durham area. As a Lead QA Tech at Lilly, your day will be filled with engaging responsibilities, from actively monitoring Good Manufacturing Practices to ensuring our quality systems are in top shape. You’ll work closely with multi-functional teams supporting production functions like formulation, filling, and visual inspection. Your keen attention to detail will shine as you review and approve essential GMP documentation, ensuring that all operations comply with the highest standards of safety and quality. Plus, your role in guiding and assisting teams will help maintain the integrity of our products. We’re looking for candidates who take pride in their work, have demonstrated experience in aseptic manufacturing, and possess a strong ability to communicate effectively. Join us at Lilly, where we not only make medications but also make a difference, and be part of our commitment to improving the health of people worldwide. If you’re ready to take the next step in your career with a respected leader in healthcare, this role is your chance to shine!
As the Associate Director – Launch Leader at Lilly, you'll spearhead manufacturing strategies and product launches within a collaborative healthcare environment.
Join Lilly as a Lead Engineering Technician, where you'll contribute to the maintenance and reliability of critical utility systems in a global healthcare environment.
Suffolk is on the lookout for a Construction QA/QC Assistant Manager with data center expertise to uphold our commitment to quality in project execution.
SQA Services is looking for a detail-oriented Data Migration Specialist to join their quality assurance team in Miami, delivering top-notch service across various industries.
Join AHS as a Design Execution Quality Assurance Officer to oversee and enhance quality standards in luxury real estate projects.
Seeking a detail-oriented Quality Engineer to lead quality assurance efforts and ensure product excellence in our operations.
Join LogiSense as a Software Tester and play a key role in shaping the future of usage-based billing for leading enterprises.
Join Octopus by RTG as a Senior QC & QA Specialist and help shape the future of AI in a rapidly expanding digital hub.
Join Mission Healthcare as a Quality Care Manager to ensure exceptional and compliant care for patients in a supportive environment.
Join the American Express team as an Analyst I-Quality, where you'll lead testing strategies and enhance transaction processes for millions of users.
Subscribe to Rise newsletter