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- Tasks: Lead a team in auditing and ensuring compliance in pharmaceutical manufacturing.
- Company: Join Lilly, a global healthcare leader dedicated to improving lives through innovative medicines.
- Benefits: Enjoy a supportive work culture with opportunities for personal development and travel.
- Why this job: Be part of a mission-driven team that values quality and compliance in healthcare.
- Qualifications: Requires a Bachelor's degree and 10 years of relevant industry experience.
- Other info: Must be open to international travel and work in a manufacturing environment.
The predicted salary is between 43200 - 72000 £ per year.
Associate Director – GQAAC GMP Pharmaceutical page is loaded
Associate Director – GQAAC GMP Pharmaceutical
Apply locations UK, Basingstoke Germany, Bad Homburg FR: Paris Spain, Albacete Italy, Trieste time type Full time posted on Posted Yesterday time left to apply End Date: August 10, 2025 (9 days left to apply) job requisition id R-88455
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.
Position Brand Description:
The Assoc. Director – GQAAC GMP Pharmaceutical role is part of the Global Quality Auditing and Compliance (GQAAC) division and represents the Global Quality Auditing interface for the commercial manufacturing organization.The position assures that an effective audit program is maintained that monitors global Lilly operations and Contract Manufacturers. It ensures that operations are performed in accordance with company standards, policies, practices and procedures and are compliant with current regulations and guidelines.This position involves supervision of an auditing staff that audits Lilly operations, both internally and externally (contracted), in support of the GQA Audit Strategy and in performance of Quality Due Diligence.
GQAAC is a valued business partner and takes a proactive approach to further enhancing the quality of business operations and regulatory compliance. The Assoc. Director – GQAAC GMP Pharmaceutical plays a key part in contributing to the implementation of this strategic approach to quality auditing and oversight within Lilly.
Key Objectives/Deliverables:
1. Team Management
- Provide leadership and supervision to auditing team
- Ensure that staff receives appropriate training and is aligned at appropriate staffing level
- Ensure development of employee skills and knowledge to allow proficient execution of responsibilities.
- Work with management team to set departmental strategy and objectives.
- Ensure all direct reporting employees have a performance management and development plan in place and carry out their objectives and responsibilities.
2. Business/Strategic Leadership/Auditing
- Work with management team to develop audit plan for auditable units within area of responsibility that aligns with the overall departmental audit plan for the corporation
- Ensure audit processes are robust and ensure qualified personnel are assigned to product/project support and audit teams; direct resources in the execution of audit plan
- Ensure consistency between audits
- Review and approve audit and assessment reports and summaries in alignment with expectations
- Perform site audits
- Develop with management team, communications on audit findings to senior management
- Escalate any significant compliance issues to relevant site, development and quality management
3. Standards
- Review and provide input to departmental corporate standards, policies and procedures
- Ensure consistency of content of standards with requirements
4. Personal Development and Shared Learning
- Attend training courses, conferences or association meetings to continue to gain knowledge; share such information with other members of the team or company to increase awareness and to train others in the implementation of these practices
- Be continually aware of current industry trends and regulatory agency interpretation of GMP and other relevant requirements
- Continue to gain knowledge necessary to provide a greater understanding of GMP requirements
5. Divisional/Global Quality Organization Support
- Participate in projects as directed by Sr. Director, Global Quality Auditing & Compliance that support or enhance GMP compliance of larger quality organization’s ability to carry out mission and meet objectives
- Participate in global projects/work groups as representative of GQAAC
Minimum Requirements:
- Minimum Bachelor’s Degree in Pharmacy, Chemistry, Biology, Engineering, Microbiology, or other technical areas of study
- Minimum of 10 years relevant industry experience in areas that must include: quality assurance or quality control
Additional Preferences:
- Experience in development operations, manufacturing operations or technical services in addition to quality is preferred
- Demonstrated ability to communicate and deliver constructive feedback to customers, including excellent oral and written communication and oral presentation skills
- Demonstrated ability to interpret and apply standards to different situations by understanding customer needs and applying good problem-solving skills
- Ability to work independently and as part of a team with minimal supervision
- Travel
- Previous auditing experience
Other Information:
- Must be able to work in a manufacturing environment
- Individual must not be sensitive to penicillin/cephalosporin
- Must be able to travel 25-35% including international travel
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.
Lillydoes not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLillyUKandIreland
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At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world.How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!
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Associate Director - GQAAC GMP Pharmaceutical employer: Eli Lilly and Company
Contact Detail:
Eli Lilly and Company Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director - GQAAC GMP Pharmaceutical
✨Tip Number 1
Familiarise yourself with the latest GMP regulations and guidelines. Understanding these will not only help you in interviews but also demonstrate your commitment to quality assurance and compliance, which is crucial for the Associate Director role.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those involved in quality auditing and compliance. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the field.
✨Tip Number 3
Prepare to discuss your leadership experience in managing teams and projects. The role requires strong team management skills, so be ready to share specific examples of how you've successfully led teams in previous positions.
✨Tip Number 4
Research Lilly's corporate culture and values. Understanding their mission to improve lives through healthcare will help you align your responses during interviews and show that you're a good fit for their team.
We think you need these skills to ace Associate Director - GQAAC GMP Pharmaceutical
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality assurance or quality control, as well as any leadership roles you've held. Use keywords from the job description to demonstrate that you meet the specific requirements for the Associate Director position.
Craft a Compelling Cover Letter: In your cover letter, express your passion for improving healthcare and how your background aligns with Lilly's mission. Mention specific experiences that showcase your ability to lead auditing teams and manage compliance effectively.
Highlight Relevant Skills: Emphasise your communication skills, problem-solving abilities, and experience in developing audit plans. Provide examples of how you've successfully navigated compliance issues in previous roles to show your capability in this area.
Proofread and Edit: Before submitting your application, carefully proofread your documents for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role in quality auditing.
How to prepare for a job interview at Eli Lilly and Company
✨Understand the Role
Make sure you have a solid grasp of the Associate Director - GQAAC GMP Pharmaceutical role. Familiarise yourself with the key responsibilities, such as team management and audit processes, so you can discuss how your experience aligns with these requirements.
✨Showcase Leadership Skills
Since this position involves leading an auditing team, be prepared to share examples of your leadership experience. Discuss how you've developed team members and managed performance, as well as any strategies you've implemented to enhance team effectiveness.
✨Prepare for Technical Questions
Expect questions related to quality assurance and compliance standards. Brush up on your knowledge of GMP regulations and be ready to discuss how you've applied these in previous roles, especially in auditing or quality control contexts.
✨Demonstrate Communication Skills
Effective communication is crucial for this role. Be ready to provide examples of how you've communicated audit findings to senior management or collaborated with cross-functional teams. Highlight your ability to give constructive feedback and present complex information clearly.
