Company Overview

Lilly, a leading innovation-driven corporation is developing a growing portfolio of pharmaceutical products by applying the latest research from its own worldwide laboratories and from collaborations with eminent scientific organizations.u00A0 Headquartered in Indianapolis, Indiana, Lilly makes life better u2013 through medicines and information u2013 for some of the worldu2019s most urgent medical needs.u00A0 Founded over 145 years ago, the company has sustained a culture that values excellence, integrity and respect for people. This has resulted in Lilly frequently being ranked as one of the best companies in the world at which to work.u00A0 Lilly knows its business has prospered because of its employees u2013 people with a talent for innovation and a passion for making a difference by finding treatments for the most stubborn diseases people whose talent is matched by their generosity, and people with strong values and a determination to prevail, regardless of the challenges.u00A0 Join our team u2013 and make a difference in improving health for people all over the world!

Manufacturing and Quality Technical Hub Hyderabad

Lilly has made a strategic investment of more than $1B dollars to establish a Manufacturing and Quality technical hub. This hub will oversee the significant investment in contract manufacturing of starting materials and intermediates for API manufacturing in India and the technical services responsible for managing the scientific agenda for manufacturing and quality. The hub will be recruiting top talent in the areas of process engineering, chemistry, analytical and data sciences to build a cutting-edge scientific organization supporting the exciting manufacturing portfolio of Lilly.

Job Description

Role Overview and Key Responsibilities:

The employee leads technical aspects of drug substance process optimization, technicalu00A0transfersu00A0and development of the technical agenda.u202F This position requires comprehensive knowledge of the pharmaceutical industry, Good Manufacturing Practices (GMP), regulatory requirements, and the essential role scientists play in making medicine and creating real-world solutions. The successful candidate should have a provenu00A0track recordu00A0of driving technical agendas and influence externally in theu00A0small moleculeu00A0space.u00A0

Provides technical support and performs analytical development work for peptide synthesis/Process development lab process development through design and execution of experiments and development of analytical methods.

This role expects to work in lab along with fellow scientists.

Key Responsibilities:

Safety culture lab management:

To ensure that appropriate personal protective equipment in the laboratory premises are available and follows the safety precautions.
Ensure the good administration and housekeeping of the PRD department work area.

Scientific & Technical Leadership

Work in the ab along with the team, provide analytical supportu00A0to commercial process optimization team, in peptides down and up streams. Leverage internal and externalu00A0expertiseu00A0to improve existing production processesu00A0 Establish a world classu00A0methodologyu00A0to ensure analytical methods and techniques are robust, cost effective and can be transitioned safely and rapidly into production environment.u00A0 Lead the successful transfer ofu00A0new/developed analytical methods across the globeu00A0 Maintain a thorough understanding of the state of the art of analytical and regulatory requirements and build these into our processesu00A0 Develop strong working relationships with both R&D and plant sites to ensure successu00A0 Serves as a member of multidisciplinary product development teams responsible for the analytical method for commercial scale processes. He/she typically directs the laboratory activities and development of one or more junior staff membersu00A0 Participateu00A0in theu00A0Science Lead Teamu2013 part of scientific governance/oversight as neededu00A0 Provide technical stewardship on all products they are accountable for.u00A0 Define andu00A0lead assignedu00A0technical projects (experimental,u00A0modelling,u00A0and/or production data analysis) to improve process control, yield,u00A0purity,u00A0and/or productivity.u00A0u00A0u00A0 Theu00A0Advisor/Senioru00A0advisoru00A0should also have a provenu00A0track recordu00A0in the following areas.u00A0

Demonstrated ability to commercialize and solve analytical problems.u00A0

Hands on experience supporting method development and transfer activities

Provenu00A0track recordu00A0of working with diverse groups across the value chain and in multiple locationsu00A0u00A0

Significant experienceu00A0with registration, includingu00A0authoringu00A0technical reports, Development History Report, regulatory responses, or direct interactions with regulatory agencies.u00A0

Understanding the scientific principles(analytical front) required for manufacturing intermediates and drug substances, including the interaction of chemistry and equipment.u00A0

Understand the chemistry and stability of peptides from a first principles perspective.u00A0

Proven record of embracing advanced digitization efforts by deploying digital tools to enableu00A0advanced modellingu00A0and seamless digital technology transferu00A0

Exhibit coaching and mentoring of peers and other scientists.u00A0

Understand instrumentation including LC, GC, titration, and mass spectrometryu00A0and expertise in PAT tools
Provide technical support to process development areas if neededu00A0
Participate in technology transfer of analytical methodsu00A0
Document all work in an appropriate manneru00A0

In carrying out his/her responsibilities, theu00A0individualu00A0is expected to work very closely with fellow scientists across the various disciplines and build up a network of contacts across the corporation and the broader scientific community. He/she must have the interpersonal skillsu00A0requiredu00A0to work effectively with a broad spectrum of people.u00A0

Education Requirement:

Ph.D. in scientific disciplines of Chemistry and Analytical chemistry /Ph.D + Post Doc in Analytical Chemistry (focusing more process chemistry) with 5-12 years

Other Information:

Some travel (domestic and international) less than 5% may be required.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form () for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lillyu00A0does 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.

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