Post-Doctoral Scientist at Eli Lilly and Company

Carolina, Puerto Rico, Puerto Rico

Eli Lilly and Company Logo
Not SpecifiedCompensation
Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, BiotechnologyIndustries

Requirements

  • PhD in a life science related field (Biochemistry, Chemistry, Biology, Biotechnology, Chemical Engineering, or Bioengineering)
  • Preferred background in lab-scale fermentation and filtration
  • Proven record of scientific publications
  • Expertise in protein purification, separation, characterization, material analysis, statistical data interpretation, technical writing, and project management
  • Strong interpersonal skills and ability to establish positive relationships and interact effectively with diverse teams
  • Excellent organizational and multitasking abilities to manage multiple assignments in a fast-paced environment
  • Demonstrated leadership capabilities
  • High attention to detail and ability to work under minimal supervision
  • Effective communication and training skills to share technical knowledge and lead process education sessions
  • Adaptability and resilience in a dynamic, 24/7 operational environment

Responsibilities

  • Serving as the subject matter expert on assigned manufacturing steps or equipment; communicating the scientific and operational strategy, including key process parameters and critical quality attributes
  • Maintaining essential documentation such as process flow diagrams and technical reports
  • Ensuring ongoing validation and capability through process monitoring, verification, and annual product review
  • Leading and participating in cleaning, validation, and bioburden control initiatives
  • Applying statistical analysis and process data to minimize variability and drive improvements
  • Conducting root cause analyses and investigating incidents; managing events, complaints, CAPAs, and changes
  • Training team members and operators; delivering process-related education at campaign starts or annually
  • Supporting daily manufacturing operations and new process introductions
  • Maintaining regulatory, safety, and environmental compliance
  • Collaborating with internal and external stakeholders, including production, maintenance, engineering, quality assurance, and external contractors

Skills

process validation
statistical analysis
root cause analysis
CAPA
process monitoring
bioburden control
manufacturing processes
technical documentation
process flow diagrams
regulatory compliance

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters
1876Year Founded
$1,180.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.
Potential construction delays in Indiana could affect GLP-1 drug production timelines.
Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.
Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.
FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.
Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.
Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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