Are you looking for an exciting opportunity to advance your career in the pharmaceutical industry? Pharmabharat.com is proud to feature the Associate Director, Quality Control – Microbiology position available at Lilly’s state-of-the-art facility in Alzey, Rhineland-Palatinate, Germany. As a global healthcare leader, Lilly is dedicated to improving lives through innovative solutions and is actively expanding its manufacturing footprint to meet the growing needs of patients worldwide.
About Lilly
Lilly, headquartered in Indianapolis, Indiana, has long been a pioneer in healthcare innovation. With a mission to unite caring with discovery, Lilly’s employees work tirelessly to develop life-changing medicines and contribute to community well-being. If you share Lilly’s commitment to making life better for people around the world, this position might be your next big step.
Position Overview
The Associate Director, Quality Control (QC) – Microbiology will play a vital role in Lily’s ambitious growth strategy. This leadership position is responsible for overseeing the QC operations specific to microbiological testing and environmental monitoring. You will partner with the Senior Director of Quality Control to cultivate a robust quality and safety culture within Lilly’s global organization.
Your responsibilities will include implementing the Quality Management System in the laboratory, ensuring compliance with regulatory requirements, and working cross-functionally to foster an environment of excellence and reliability.
Key Responsibilities
As an Associate Director, you will:
- Lead Laboratory Operations: Collaborate with global teams to drive comprehensive laboratory management, ensuring all methods, utilities, and equipment align with strategic goals.
- Team Development: spearhead talent acquisition for the laboratory, enhancing team diversity and capabilities necessary for effective laboratory function.
- Establish Compliance Standards: Create and maintain laboratory operations that comply with Lilly’s Global Quality Standards and regulatory guidelines—with an emphasis on continuous improvement.
- Performance Management: Monitor laboratory costs and oversee contractors to optimize operational efficiency.
- Create a Strong Quality Culture: Promote open communication and teamwork within the workgroup to enhance workforce engagement in achieving shared objectives.
- Lead Audits and Inspections: Prepare for and manage interactions with regulatory agencies, ensuring full compliance with cGMP requirements.
Basic Qualifications
To excel in this role, we are seeking candidates who meet the following criteria:
- A Bachelor of Science degree or equivalent in a scientific field; a focus on microbiology is preferred.
- At least 5 years of GMP Quality Control Laboratory experience, particularly in microbiological testing and environmental monitoring.
- A minimum of 5 years of leadership experience within Quality Control, specifically in parenteral operations.
Additional Skills
Preference will be given to candidates who possess:
- In-depth knowledge of compliance and regulatory requirements.
- Experience in regulatory inspections and audit readiness.
- Proven problem-solving abilities and excellent technical writing skills.
- Familiarity with electronic laboratory management systems like LIMS.
Why Join Lilly?
This position offers you the opportunity to work in a fast-paced environment where innovation is promoted and employees are supported in their professional journey. With a flexible working arrangement, Lilly values work-life balance, allowing for periodic remote work based on project conditions.
Important Information
- Location: Alzey, Germany
- Work Environment: On-site presence required, with the possibility of remote work (up to 4 days a month).
- Occasional travel (10-20%) may be needed for site benchmarking and training initiatives.
Lilly is committed to offering equal employment opportunities and welcomes individuals with disabilities to apply. For more information on the application process, please complete the accommodation request form.
