Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
L
Lilly
Molecule Steward
Career Insights for Environmental Compliance Specialist
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on North Carolina data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
An Environmental Compliance Specialist performs environmental audits and advises companies on compliance with state, local and federal environmental regulations. Investigates company waste disposal, industrial hygiene and pesticide use practices and policies, advises on compliance issues and reports violations as needed.
$86,835 / year median in North Carolina
+14% projected growth
Job Description
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Responsibilities:
The mission of Technical Services/Manufacturing Sciences (TS/MS) is to provide scientific leadership and technical support for manufacturing to make medicine. The Site Molecule Steward is the subject matter expert for the Concord Site Drug Product manufacturing and will provide local technical leadership and expertise for projects involving TS/MS.Key Objectives/Deliverables:
- Assume ownership of control strategy implementation and execution at the manufacturing site.
- Interact with peers across the parenteral network, including TS/MS, QA, QC, Regulatory and Engineering, both site and central
- Share learning and ensure strategies are in line with technical, quality, and regulatory guidance, while supporting business expectations.
- Play a critical role in technical capability building and coaching at the site to ensure capabilities are in place to meet business objectives.
- Serve as technical subject matter expert for all topics related to drug product manufacturing.
- Expected to provide technical direction on deviations, production challenges, and impact assessment of change controls.
- Represent the TS/MS function in regulatory interactions, as needed.
- Be responsible and influential with respect to implementation of external/corporate trends and understanding of how these changes could impact the Concord site.
- Excellent technical writing and oral communication skills along with the ability to effectively communicate and transfer knowledge to all levels of the organization.
- Although not a supervisory role, technical leadership, and the ability to cross functionally influence are important in this role.
Basic Qualifications:
- Minimum of bachelor's degree in science or engineering field,
- Minimum of 5 years directly supporting parenteral product manufacturing.
Additional Skills/Preferences:
- Strong communication skills
- Capability to prioritize and multi-task effectively.
- Collaborate with other functions as teams as appropriate.
Additional Information:
- This position is tech ladder approved (R4+). Position final level will be based upon the level of the candidate chosen.
- This position will be required to collaborate with peers across the network (Indianapolis, France, RTP) in certain situations.
- This position is day shift, Monday-Friday, with off hours support needed, by request.