- Expiry Date: 09 August 2021
We are seeking a skilled Project manager with experience in biopharmaceutical technical process development, technology transfer and/or regulatory submissions in Chemistry, Manufacturing and Controls (CMC) space. The person will be responsible for projects that may include process development, tech transfer from one site to another and regulatory submissions components. Previous experience (as a scientist or project manager) in one or more of these areas is a must. Experience and/or training in Project Management is a must. Responsibilities include: Project Plans Develop project plans for timelines and resources. Manage team meetings - Setting agendas, maintaining action tracker and decision logs. Reporting Preparing weekly dashboards on program status in collaboration with technical leads Resources interface with finance to provide actual and forecast HC and spend The person will work in collaboration with an MSAT Business Partner. The position is in the CMC Project Management & Tech Transfer group within Global MSAT (Manufacturing Science & Analytical Technology) in Industrial Affairs. Musts: Experience in MS Teams, MS Word, Powerpoint, Excel, MS Project (or other project planning tool). At least 3 years experience in Project Management At least one of the following: experience in biologics drug substance or drug product technology transfer, process development and/or regulatory submissions.
Strong Communication skills
Bachelors , Master or PhD in life sciences or engineering required.
Experience in MS Teams, MS Word, Powerpoint, Excel, MS Project (or other project planning tool).
Experience in biologics drug substance or drug product technology transfer, process development and/or regulatory submissions.
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