Scientist - Drug Product Process Development
Scientist - Drug Product Process Development
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Scientist,Drug Product Process Development - Berkshire, England - 12 Months Contract
We are looking for an experienced Scientist - Drug Product Process Development for a fantastic 12 months contract based in Berkshire.
You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease.
This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first.
Responsibilities
* Technical expert in the establishment of robust, fit for purpose injectable drug product manufacturing processes from toxicology studies or first in human until BLA approval.
* Define and select drug product manufacturing processes and parameters for clinical manufacture.
* Cooperate with a wide range of internal and external stakeholders, including contract manufacturing organisations, as part of a project team.
* Design and execution of lab studies in relation to drug product development activities, capture and analyze data and author related documentation (write-ups, protocols, reports (eg filter selection and sizing, target fill volume assessment, compatibility assessments, clinical blinding, etc)
* Capture and analyse critical manufacturing process data for process understanding and process characterisation
* Perform process risk assessments
* Design DP processes for sterile injectable drug products in liquid or lyophilized powder form, in vials, pre-filled syringes or as combination products),
* Define the investigational medicine product preparation process in clinical trials.
Requirements:
* Extensive experience in liquid drug product development and/or manufacturing within the pharmaceutical industry is required.
* Experience within the bio pharmaceutical industry is an advantage.
* Knowledge and technical experience in liquid drug product development and cGMP manufacturing under aseptic conditions (such as vial, cartridge and pre-filled syringe filling) Is an advantage.
* Technical knowledge of sterile DP development covering DP components, process transfer, scale-up and optimisation is an advantage.
If this role is of interest to you, please apply now!
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Job function
Research, Analyst, and Information Technology
* Industries
Staffing and Recruiting
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