Lilly Consultant Scientist, Parental Pilot Plant in Indiana

32705BR

Title Consultant Scientist, Parental Pilot Plant

State / Province Indiana

Country USA

Workplace Arrangement Local

Company Overview 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 39,000 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.

Lilly currently has openings at its Greenfield, Indiana location for the following position:

Responsibilities Req ID 32705BR - Consultant Scientist, Parental Pilot Plant: Support a wide range of activities to enable the parenteral manufacturing network in the efficient manufacturing of high quality medicines to provide successful patient outcomes. These activities include process development, scale-up, and technical transfer of new and existing products; evaluation of new materials and equipment technologies; and studies to support process improvements and improved control strategies. Provide technical leadership within a cross-functional team environment to advance the different technical initiatives through utilizing the technical capabilities and human resources of the pilot plant in collaboration with global manufacturing and development teams. Lead and support sterile, manufacturing improvement related projects. Support the manufacturing site’s process investigations, identify root causes, and develop corrective and preventive action plans. Drive pilot plant facility improvements to maintain capabilities commensurate with manufacturing needs. Confirm the required equipment and resources are in place for the pilot facility to be effective in meeting customer needs. Design and execute the necessary pilot plant studies, including writing protocols and reports. Conduct design of experiments and interpret data. Perform process capability assessments and investigate out of control signals. Support the manufacturing site’s process validation during the different lifecycle phases and sterilization qualifications. Maintain and enforce the highest safety standards and create a safe work environment in the facility. Ensure environmental impact concerns are considered during project planning discussions.

Basic Qualifications Employer requires a Master of Science degree in Biochemistry, Chemistry, Chemical Engineering, Pharmaceutical Science, or a related field, and at least 8 years experience in the pharmaceutical/biotech industry. Employer will also accept a Bachelor of Science degree in Biochemistry, Chemistry, Chemical Engineering, Pharmaceutical Science, or a related field, and at least 10 years experience in the pharmaceutical/biotech industry.Work or academic experience must have included the following:Parenteral pharmaceutical manufacturing equipment and processes; Developing and implementing manufacturing process improvements; Manufacturing of protein-based pharmaceutical products; Freeze drying; Project management; Product formulation and parenteral aseptic processing; cGMP, experimental design, statistical analysis, or development of control strategies for parenteral products; and Developing sterilization procedure, environmental monitoring risk based strategies and sampling plans.

Additional Information Please submit resume via www.lilly.com/careers and cite the relevant job title and req I.D. number in your submission.

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.

Removal Date 19-May-2017