Eyecare Sterile Formulation Lead Scientist

ABBVIE

Irvine (CA)

On-site

USD 142,000 - 269,000

Full time

9 days ago
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Job summary

AbbVie in Irvine, CA is seeking a Principal Research Scientist II/Associate Director for Eyecare to lead sterile liquid dosage-form development and associated regulatory activities. The role includes directing strategies for new products through clinical trials, regulatory submission, and commercialization with a focus on eyecare products.

The position requires strong scientific leadership, collaboration with CROs/CMOs, and the ability to coach staff while upholding GLP/GMP standards and safety

Qualifications

  • Bachelor’s Degree in Science related field with extensive related work experience.
  • Master’s Degree in Science or PharmD with extensive related work experience.
  • PhD in Science or related field with extensive related work experience.

Responsibilities

  • Provide scientific and technical leadership for sterile eyecare formulation and development.
  • Direct formulation and process-development strategies for products for clinical trials and commercialization.
  • Develop and maintain knowledge of global CMC submission requirements and GLP/GMP expectations.
  • Advance development through regulatory filings, technology transfer, and collaborations with CROs/CMOs.
  • Lead, coach, and develop direct reports while ensuring laboratory safety and quality.

Skills

Leadership
Cross-functional collaboration
Quality by Design
Statistical analysis

Education

Bachelor’s Degree in Science related field
Master’s Degree in Science or PharmD
PhD in Science or related field

Tools

JMP

Job description

AbbVie in Irvine, CA is seeking a Principal Research Scientist II/Associate Director for Eyecare to lead sterile liquid dosage-form development and associated regulatory activities. The role includes directing strategies for new products through clinical trials, regulatory submission, and commercialization with a focus on eyecare products.

The position requires strong scientific leadership, collaboration with CROs/CMOs, and the ability to coach staff while upholding GLP/GMP standards and safety

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