
Advisor, Contamination Control Strategy – Lebanon API Manufacturing
- Lebanon, IN
- $76,500-181,500 per year
- Permanent
- Full-time
- Assess differences in current CCS programs across the sites (internal and external) and drive harmonization at the Lilly Lebanon API Manufacturing site.
- Work closely with site and cross-functional SMEs to drive alignment. Ensure control strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved.
- Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability. Apply process knowledge and data analysis skills to support the management of daily manufacturing operations.
- Represent TS/MS across network governance forums and ensure that CCS programs are frequently presented to network team in order to achieve alignment across sites.
- Ensure that learnings and best practices are shared across sites.
- Set-up appropriate forums in order to share learnings and present case studies to site SMEs.
- Provide CCS technical support both for the initial start-up of the manufacturing areas as well as post Process Validation support.
- Understand and support global implementation of quality standards, best practices, and appropriate tools to ensure strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved.
- Engage in providing support during regulatory interactions including on-site inspections. Support regulatory submissions and site audits to ensure holistic assessment of CCS.
- Ability to influence and communicate to diverse groups on complex regulatory, business, or technical CCS issues within the site and function.
- Provides foundational understanding of contamination control standards and strategies to support qualification of new flexible manufacturing facilities and processes.
- Understands the scientific principles required for manufacturing drug substance, including interaction of the chemistry, equipment, and contamination control strategies.
- Able to influence teams and build understanding of CCS functions across site.
- Works within cross-functional teams in a positive fashion to implement TS/MS objectives and deliver on business plan and contamination control objectives.
- Ability to author, review, and/or approve technical documents, including personnel qualification strategies for technical staff, control strategies, investigations, change controls, expert opinions, qualifications, procedures, technical studies, etc.
- Minimum BS degree required in biological science or engineering discipline (Microbiology-preferred, Biology, Chemistry, Mechanical/Chemical/Biomedical Engineering, etc.).
- 10+ years experience including 5 years GMP experience
- Deep technical understanding of contamination control strategies, including regulatory expectations pertaining to all elements of contamination control: manufacturing facilities, production practices, equipment cleaning and validation, environmental monitoring, bioburden controls and other product protection control related systems.
- Strong knowledge of pharmaceutical manufacturing processes, facility start-up procedures, and GMP regulations.
- Prefer 10+ years of progressively responsible experience directly supporting contamination controls within pharmaceutical manufacturing environment.
- Proficiency in delivering highly complex tasks and/or tasks that are highly cross-functional
- Proficiency in data analysis, ability to prioritize, attention to detail, critical decision-making skills, complex problem-solving abilities
- Strong analytical and quantitative problem-solving skills
- Experience in statistics
- Strategic thinking and ability to balance short term needs with long term business evolution
- Ability to mentor and develop scientists and engineers in contamination control principles, applications and applied pharmaceutical microbiology
- Technical writing and communication skills are used daily and the ability to effectively communicate and transfer knowledge to all levels of the organization is essential.
- Demonstrated experience influencing site and network leaders to advance technical agenda projects
- This is a fully on-site position located in Lebanon, IN
- This position could require some travel (including international), less than 10%
- This position is day shift, Monday-Friday, with off-hours support needed, by request