Associate Director – Technical Services/Manufacturing Science (TS/MS) Purification - Lebanon API

Eli Lilly and Company; Lebanon (IN); On-site; USD 80,000 - 130,000; Full time

Job summary

Join a forward-thinking company as an Associate Director in a groundbreaking manufacturing facility. This role offers a unique chance to lead a team in ensuring the quality and compliance of drug manufacturing processes. You will play a crucial part in developing technical capabilities and overseeing the manufacturing of life-saving medicines. The ideal candidate will possess strong technical leadership and problem-solving skills, along with a commitment to teamwork and collaboration. If you're passionate about making a difference in healthcare and thrive in a dynamic environment, this opportunity is for you!

Qualifications

• 5+ years in Technical Services or Pharmaceutical Manufacturing.
• 1+ year of supervisory experience in a relevant industry.

Responsibilities

• Lead TS/MS scientists on technical oversight of manufacturing processes.
• Ensure compliance with regulatory requirements and cGMPs.
• Develop technical capabilities within the team.

Skills

Technical writing

Interpersonal skills

Problem-solving

Knowledge of cGMP

Teamwork

Technical leadership

Strategic thinking

Education

Bachelor's Degree in Chemistry or related field

Job description

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.

Job Description

Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN. This facility is Lilly’s largest investment in manufacturing capacity and is intended to provide APIs for current and future products. This is a unique opportunity to be a part of the leadership team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

Job Overview

The TS/MS organization provides technical oversight to ensure robust and consistent biology and chemistry throughout all aspects of the manufacturing process. Through cross functional collaboration, TS/MS ensures the quality and safety of our products through process monitoring and knowledge to control, prevent and mitigate variability to deliver a reliable supply of medicine.

The Associate Director is primarily responsible to lead TS/MS scientists’ team on the technical oversight of the manufacturing process with the purpose of ensuring the reliable and compliant manufacturing of bulk drug substance. Additionally, this role partners with other roles within the TS/MS organization and other functional disciplines to support the functional and site objectives.

Responsibilities:

The successful candidate is responsible for:

• Ensuring that the team has a fully understanding of the protein chemistry, control strategy, and manufacturing platform related to the purification process of drug bulk substance.
• Prioritization and execution of routine process monitoring, manufacturing support and that processes remain in control and capable in accordance with regulatory requirements and cGMPs.
• Development of technical capabilities within the technical staff and performance management.
• Providing technical leadership for the preparation, review and approval of technical documents including investigations, change controls, manufacturing tickets, periodic product reviews, process validation and other technical documents.
• Acting as the primary technical representative in a cross-functional setting on Flow Team Meeting, Deviation Board, etc.
• Leading the development and execution of process validation, process changes and implementation of technical agenda projects with the collaboration of the secondary loop and other functions.

Basic Qualifications

• Bachelor's Degree in scientific disciplines of Chemistry, Biochemistry, Microbiology, Protein Chemistry, Biophysical Chemistry, Bioanalytical Chemistry, or Bio/Chemical Engineering.
• 5+ years of experience in any of the following disciplines such as Technical Services, Pharmaceutical Manufacturing, Protein Manufacturing, Quality Control, Quality Assurance, product and/or process development or Engineering.
• 1+ year of supervisory experience in a relevant industry.

Other Requirements

• Technical writing and presentation skills.
• Excellent interpersonal skills that promote engagement and teamwork within cross-functional environment.
• Knowledge of cGMP, applicable global regulatory manufacturing guidance, and the process/cleaning validation in drug substance pharmaceutical manufacturing are a plus. Flexibility is required to support site needs in a 24/7 environment.
• Teamwork oriented.
• Demonstrated ability to learn and apply technical/scientific knowledge Ability to communicate and effectively influence across functional groups and stakeholders.
• Technical leadership, administrative and organization skills.
• Strong problem-solving skills.
• Proficiency in delivering highly complex tasks and/or tasks that are highly cross-functional. Strategic thinking and ability to balance short term needs with long term business goals.