Bioprocess Purification Scientist — Development & Transfer

Initial Therapeutics, Inc.

Indianapolis (IN)

On-site

USD 80,000 - 117,000

Full time

14 days+

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Job summary

Lilly, headquartered in Indianapolis, Indiana, is seeking a scientist to advance downstream purification development for bioproducts. The role involves defining purification processes, transferring methods to pilot plants and manufacturing sites, and drafting regulatorydocumentation.

Collaboration with Bioprocess/Bioproduct Development and Manufacturing teams is essential. The candidate will contribute to process robustness studies, technology transfer, and regulatory submissions, while

Qualifications

  • BS or MS degree in Chemical Engineering, Biochemistry, Chemistry or related field with 5+ years (BS) or 2+ years (MS) of direct related industry experience.
  • PhD will not be considered at this job level.
  • Biochemistry experience with some knowledge of protein chemistry and protein purification.

Responsibilities

  • Design, execute and interpret appropriate purification development experiments for generation of bioproduct active pharmaceutical ingredient.
  • Participate in cross-functional process development teams and effectively collaborate with other groups in Bioprocess and Bioproduct Development, Discovery, Technical services for Manufacturing and Manufacturing.
  • Support transfer of purification processes to pilot plant and manufacturing sites.
  • Author technical reports and regulatory documents.
  • Work effectively with external parties on development projects, research collaborations and outsourcing efforts.
  • Support organizational initiatives, as appropriate
  • Keep abreast of relevant scientific literature, new technologies/capabilities and regulatory initiatives/requirements and support their implementation, as appropriate.
  • Supervision of personnel and coaching, training and administration of performance management to personnel, where assigned.
  • Ensure work is aligned with all relevant Development Quality, Regulatory, HSE, GLP and GMP requirements.

Skills

Bioprocess development
Purification development
Regulatory documentation
Team collaboration
DOE experience

Education

BS/MS in Chemical Engineering, Biochemistry, Chemistry or related
MS/BS with required experience

Job description

Lilly, headquartered in Indianapolis, Indiana, is seeking a scientist to advance downstream purification development for bioproducts. The role involves defining purification processes, transferring methods to pilot plants and manufacturing sites, and drafting regulatorydocumentation.

Collaboration with Bioprocess/Bioproduct Development and Manufacturing teams is essential. The candidate will contribute to process robustness studies, technology transfer, and regulatory submissions, while

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