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Lead QA Tech - Parenteral

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 - $51.68

Full-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

Average salary estimate

$82806.5 / YEARLY (est.)
min
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$58141K
$107472K

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.

What You Should Know About Lead QA Tech - Parenteral, Lilly

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!

Frequently Asked Questions (FAQs) for Lead QA Tech - Parenteral Role at Lilly
What are the responsibilities of a Lead QA Tech - Parenteral at Lilly?

As a Lead QA Tech - Parenteral at Lilly, your key responsibilities include providing oversight on GMP operations, ensuring compliance with relevant quality systems, reviewing important GMP documentation, and monitoring adherence to Good Manufacturing Practices within the production areas. You'll actively engage with the team to support operational goals while also maintaining a commitment to safety and quality.

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What qualifications do you need to become a Lead QA Tech - Parenteral at Lilly?

To qualify as a Lead QA Tech - Parenteral at Lilly, a high school diploma is essential, alongside relevant pharmaceutical experience in aseptic manufacturing. While an associates degree in a related field is preferred, strong communication skills and meticulous attention to detail are crucial. Experience in Production QA and as a visual inspector will further enhance your suitability for this position.

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How does Lilly support the career growth of its Lead QA Tech - Parenteral professionals?

Lilly values the development of its employees, offering continuous training and support to Lead QA Tech - Parenteral professionals. This includes opportunities for hands-on training in various quality systems and compliance practices, mentorship programs, and various resources for professional advancement. By fostering a culture of growth, Lilly ensures its employees are equipped to excel in their roles.

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What is the work schedule like for a Lead QA Tech - Parenteral at Lilly?

The Lead QA Tech - Parenteral role at Lilly supports a 24/7 operation, primarily working in a rotating twelve-hour day shift schedule. Initially, during onboarding, you’ll work eight-hour shifts from Monday to Friday, transitioning to the rotating twelve-hour shifts upon approval. Flexibility and commitment to scheduled shifts, including potential mandatory overtime, are essential.

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What benefits can you expect as a Lead QA Tech - Parenteral at Lilly?

As a Lead QA Tech - Parenteral at Lilly, you'll enjoy a competitive compensation package, including eligibility for bonuses based on performance. Additional benefits encompass a comprehensive healthcare program, retirement plans, vacation benefits, and well-being initiatives designed to foster a healthy work-life balance. Lilly's commitment to its employees includes promoting an inclusive workplace and providing resources for personal and professional care.

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Common Interview Questions for Lead QA Tech - Parenteral
Can you describe your experience with Good Manufacturing Practices in the context of QA?

When answering this question, focus on specific examples from your past roles that illustrate your understanding of GMP. Discuss any experiences you have had in monitoring operations, training staff on GMP compliance, or any audits you have participated in. Highlight your commitment to maintaining high-quality standards and detail how you ensured adherence to GMP within teams.

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What steps do you take to ensure documentation accuracy in your QA processes?

To effectively answer this question, outline your methodical approach to documentation. Emphasize your attention to detail, your strategies for reviewing and approving documents, and your experience with quality systems like SAP or TrackWise. Providing specific examples where your approach resulted in improved accuracy will demonstrate your competence in this area.

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How do you handle non-conformance in quality processes?

When discussing your approach to handling non-conformance, explain how you identify potential issues, how you assess their impact on product quality, and what corrective actions you have taken in past experiences. Mention your collaboration with cross-functional teams to communicate findings and implement solutions effectively.

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What experience do you have with Aseptic Process Simulation?

In answering this question, provide insights into your experience with aseptic processes, detailing specific tasks you participated in, such as overseeing simulations or supporting documentation. Mention any challenges you’ve encountered during simulations, how you overcame them, and the importance of these processes in ensuring product quality.

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How do you prioritize your responsibilities when managing multiple quality oversight tasks?

Discuss your organizational and prioritization strategy in handling multiple responsibilities. Highlight techniques you employ, such as using task lists, prioritizing urgent issues based on impact, and collaborating with team members to distribute workloads effectively. Providing real examples of past projects will substantiate your methods.

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Describe a time you improved a QA process. What was the outcome?

When discussing improvements you’ve made to QA processes, outline the specific process that was enhanced, including initial challenges. Explain the changes you implemented, your reasoning, and the outcome, such as increased efficiency, better compliance rates, or enhanced team understanding. Use measurable results if possible to showcase your impact.

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What tools and software are you familiar with for quality assurance tracking?

In response to this question, list any relevant tools you have used in past positions, such as TrackWise, SAP, and Veeva. Discuss your proficiency with each tool and how you've effectively leveraged them to enhance workflow, documentation processes, and compliance tracking in your QA responsibilities.

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How do you stay current with regulations and compliance standards in the pharmaceutical industry?

Describe the methods you use to stay informed about industry regulations, such as attending conferences, completing training courses, subscribing to industry publications, or participating in professional organizations. Highlight your proactive commitment to staying updated and how you apply that knowledge within your QA role.

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What interpersonal skills do you consider important for success as a Lead QA Tech?

Discuss the importance of communication, teamwork, and problem-solving in QA roles. Provide examples of how you've utilized these skills to foster collaboration within your team, improve morale, or resolve conflicts. Articulating how your interpersonal skills lead to a positive work environment can strengthen your response.

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Why do you want to work for Lilly as a Lead QA Tech - Parenteral?

In your response, express genuine enthusiasm for Lilly’s mission and values. Highlight how the role of Lead QA Tech aligns with your career goals, how you admire the contributions Lilly makes to healthcare, and how you believe your skills and experience can help advance Lilly's commitment to quality and innovation.

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EMPLOYMENT TYPE
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DATE POSTED
April 20, 2025

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