Associate Director – Technical Services/ Manufacturing Science (TS/MS) – Validation in Indianapolis

Job Description

Join American pharmaceutical leader Eli Lilly and Company, currently hiring Associate Director – Technical Services/ Manufacturing Science (TS/MS) – Validation in Indianapolis, Apply Lilly careers in Indianapolis Indiana.


Position : Associate Director – Technical Services/ Manufacturing Science (TS/MS) – Validation

Location : Indianapolis, Indiana

Job id: R-31508


Job Details

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 35,000 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.Organization Overview: At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.Position Brand Description:Leading/mentoring a technical staff and understanding parenteral aseptic processing as it relates to drug product manufacturing.  Provide guidance on time management and priorities for direct reports.  Manage routine production support activities while balancing implementation of technical projects and process optimizations.  Key position responsibility is to address and document GMP compliance issues and development/execution of validation plans.  The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards for validation.  Influence and implement the technical agenda within a multi-discipline technical environment.  Work with peer leadership in a positive fashion to deliver on functional technical objectives, specific product business plan, and quality objectives.Key Objectives/Deliverables:Technical and defendable process support servicePerformance management and development of staffPartner within TS/MS and across functional disciplines to influence and implement the technical agenda, site business plan objectives and GMP Quality Plan objectives.Technical review and approval for site quality documents, plans, validation-related documents and studies.Minimum Requirements:Bachelors or equivalent 4 year degree in scientific disciplines of Chemistry, Biology, Pharmacy, Engineering or a related field5 years of experienceAdditional Preferences:Teamwork and interpersonal skillsTechnical leadership, administrative and organizational skillsProblem solving and independent decision making skillsMulti-tasking and communications skillsAbility to influence diverse groupsComputer and statistical analysis skillsResponsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.Additional relevant industrial experience (greater than 5 years) in any of the following associated disciplines such as Manufacturing, Quality Control, Quality Assurance, Advanced Project Management, Development, Regulatory Sciences, or Engineering.Six Sigma Green Belt or Black Belt certificationOther Information: 8 hour days –Monday through FridayOvertime will be requiredRequired to respond off shift  to operational issuesMinimal travel requiredApplicant will work in various areas within the Parenteral Plant.  Some allergens are present in the parenteral plant.  Mobility requirements and exposure to allergens should be considered when applying for this position.Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and does 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.

As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).



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