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MS&T Scientist
Employer undisclosedRole managed by a recruiter
Support drug substance manufacturing, validation & process improvement in a €1B biopharma project.
To identify and implement process improvements, e.g. yield, cycle time reduction through evaluation of process performance using data analytics tools.
Authoring of technical documents, including protocols, reports and SOPs supporting the validation of the manufacturing process.
Can effectively partner with and influence stakeholders without direct solid line authority. Drives technical decisions balancing product quality and operational requirements
To generate documentation protocols and lead the execution of plant supporting studies and technical studies on the manufacturing floor at commercial scale
What you bring
cgmp
bsc
drug manufacturing
interpersonal
upstream
downstream
You have demonstrated awareness of cGMP compliance and regulatory agency requirements as well as strong oral communication and technical writing skills.
Minimum BSc or equivalent with extensive experience in drug substance manufacturing technical support in the biopharmaceutical industry.
Good interpersonal skills coupled with demonstrated ability to effectively work in a cross-functional global environment matrix organisation, and in local group settings.
Have a thorough knowledge of the science behind the molecule and associated drug substance manufacturing processes with fundamental knowledge of upstream and downstream processes
Ability to develop, build, present and defend technical and scientific approaches in both written and verbal form.
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