上海GSK招人的广告# Returnee - 海归
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Job Title: Principal Scientist
JOB FACTORS
Job Purpose and Key Responsibilities:
Member of an R&D China team responsible for enabling the progression of NCE
’s from proof of concept to product commercialization.
Accountability:
1. Develop and supply clinical dosage forms to support clinical studies for
drugs in R&D China pipeline.
2. Contribute to the preparation of Pharmaceutical Development related
regulatory documents.
Complexity:
1. Have led teams or been part of matrix teams which have delivered drug
product for clinical or commercial use.
2. A demonstrated ability to work and deliver through others remotely.
Specialised Knowledge:
1. Have a sound knowledge of the requirements of product development through
the development lifecycle, have contributed to PPD reviews and will have
contributed to the preparation of regulatory documents.
2. Have demonstrated ability in leading formulation development for
molecules beyond FTIH .
3. Experience in formulation and process development of small molecules and
biopharmaceuticals
4. Very good understanding of physico-chemical properties and
biopharmaceutics and their relationship to formulation development.
5. Have developed and optimized processes for the manufacture of drug
products and participated in manufacture of clinical supplies.
Basic Requirements:
1. PhD in Pharmaceutics, or other related fields with significant >5 yrs of
industrial experience in pharmaceutical development
2. Excellent oral and written communication skills.
3. Must have good knowledge of cGMP requirements for product development.
Preferred Requirements:
1. Have outstanding networking and influencing capabilities.
2. Have designed and executed scale up studies and potentially have
participated in technology transfer.
Job Title: Principal Scientist
JOB FACTORS
Job Purpose and Key Responsibilities:
Member of an R&D China team responsible for enabling the progression of NCE
’s from proof of concept to product commercialization.
Accountability:
1. Develop and supply clinical dosage forms to support clinical studies for
drugs in R&D China pipeline.
2. Contribute to the preparation of Pharmaceutical Development related
regulatory documents.
Complexity:
1. Have led teams or been part of matrix teams which have delivered drug
product for clinical or commercial use.
2. A demonstrated ability to work and deliver through others remotely.
Specialised Knowledge:
1. Have a sound knowledge of the requirements of product development through
the development lifecycle, have contributed to PPD reviews and will have
contributed to the preparation of regulatory documents.
2. Have demonstrated ability in leading formulation development for
molecules beyond FTIH .
3. Experience in formulation and process development of small molecules and
biopharmaceuticals
4. Very good understanding of physico-chemical properties and
biopharmaceutics and their relationship to formulation development.
5. Have developed and optimized processes for the manufacture of drug
products and participated in manufacture of clinical supplies.
Basic Requirements:
1. PhD in Pharmaceutics, or other related fields with significant >5 yrs of
industrial experience in pharmaceutical development
2. Excellent oral and written communication skills.
3. Must have good knowledge of cGMP requirements for product development.
Preferred Requirements:
1. Have outstanding networking and influencing capabilities.
2. Have designed and executed scale up studies and potentially have
participated in technology transfer.