Lead Scientist, Formulation & Process Development

Bora Pharmaceuticals

Maple Grove (MN)

Hybrid

USD 142,000 - 185,000

Full time

14 days+

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Benefits offered by this job

Competitive salary
Health coverage
Retirement plan
Paid time off
Professional development opportunities
Wellness programs
Employee assistance program

Job summary

Bora Pharmaceuticals is a premier CDMO providing formulation development, clinical and commercial manufacturing, and packaging across complex dosage forms. This Principal Scientist will lead early-stage formulation and process development, oversee technology transfer, and support on-site client visits, tours, and quotes.

The role emphasizes process understanding, CCPs, and continuous improvement within a cGMP environment, with leadership responsibilities for junior team members and collaboration

Qualifications

  • Minimum bachelor's degree in a scientific or technical field with at least 10 years of relevant experience in pharmaceutical product development, manufacturing, and/or process development.
  • Master's degree with a minimum of 5 years of the above experience, or PhD with at least 3 years of the above experience.
  • Minimum 5 years' experience with oral solid dosage forms including formulation and process development, scale-up, tech transfer, or ongoing commercial support.

Responsibilities

  • Lead formulation and process development, scale-up, and technology transfer through commercialization and product lifecycle.
  • Directly involved in R&D/DOE, scale-up, and registration batches across development.
  • Develop and maintain process understanding by identifying CQAs, CPPs, and process control strategies.

Skills

QbD approach
Process development
Scale-up
Technology transfer
Problem solving
Leadership
Training

Education

Bachelor's degree in pharmaceutical science/chemistry/chemical engineering
Master's degree in the above field
PhD in a related field

Tools

DOE
Pilot-scale equipment

Job description

Bora Pharmaceuticals is a premier CDMO providing formulation development, clinical and commercial manufacturing, and packaging across complex dosage forms. This Principal Scientist will lead early-stage formulation and process development, oversee technology transfer, and support on-site client visits, tours, and quotes.

The role emphasizes process understanding, CCPs, and continuous improvement within a cGMP environment, with leadership responsibilities for junior team members and collaboration

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