Postdoc, Technical Services & Bioprocess Manufacturing

BioSpace

Indianapolis (IN)

On-site

USD 58,000 - 123,000

Full time

45 hours ago
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Benefits offered by this job

401(k) plan
Pension
Vacation benefits
Health benefits
Well-being program

Job summary

Lilly in Indianapolis is seeking a Post-Doctoral Scientist to support the Technical Services/Manufacturing Science (TS/MS) organization in developing and transferring commercial processes for biomolecules, including proteins, peptides, and oligonucleotides.

The role focuses on designing and executing experiments to advance process knowledge, optimize processing conditions, and enable technical transfer, with exposure to GMP and regulatory considerations in a dynamic manufacturing environment.

Qualifications

  • Ph.D. in scientific disciplines of Biochemistry, Biology, Molecular Biology, Pharmacology, Chemistry or related fields.
  • Demonstrated experience and proficiency in the areas of protein, oligonucleotide, and peptide chemistry and/or purification.
  • Requires a record of publication in peer reviewed journals and presentations / posters at scientific conferences.

Responsibilities

  • Ensuring reliability of our manufacturing systems.
  • Searching for and implementing continuous improvements.
  • Driving technical projects.
  • Maintaining our processes in a state of compliance with US and global regulations.
  • Designing and developing drug processes and delivery systems.

Skills

Protein chemistry
Oligonucleotide chemistry
Peptide chemistry
Purification

Education

Ph.D. in Biochemistry, Biology, Molecular Biology, Pharmacology, Chemistry or related fields

Job description

Lilly in Indianapolis is seeking a Post-Doctoral Scientist to support the Technical Services/Manufacturing Science (TS/MS) organization in developing and transferring commercial processes for biomolecules, including proteins, peptides, and oligonucleotides.

The role focuses on designing and executing experiments to advance process knowledge, optimize processing conditions, and enable technical transfer, with exposure to GMP and regulatory considerations in a dynamic manufacturing environment.

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