Project Manager | Process Technologies and Projects | Zuid-Holland
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Zuid-Holland Netherlands.
- Specify project requests, taking into account guidelines and procedures
– Group, prioritize and optimize those requests
- Take responsibility for gathering project requirements, define/document solutions and associated cost pictures
- Responsible for assembling project teams, identifying appropriate resources needed, develop and execute project plans, and assign individual responsibilities
- Function as a team builder for projects managed
- Track, schedule and manage issues to ensure NCS commitment dates and project deliverables are met
- Deliver projects within requested timeframe and budget
- Must have minimum 5 years Project Management experience (budgets, plan, schedule, issue tracking/remediation, risk analysis, etc.)
- At least 2 years experience managing and performing Technical Support Services contracts or tasks
- Must have GEP / GMP knowledge related to system modification/ introduction in a running GMP facility.
- Beneficial: Computer infrastructure operations or deployment background
- Beneficial: Technical writing skills to write the proper documentation according to internal regulations (FDA part 11, GxP, etc.)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
The Company
Their Vaccine Launch Facility is a state-of-the-art vaccines manufacturing facility which is designed to manufacture drug substance on a 1000 L scale for Phase III and commercial purposes. Currently the facility is in a start-up phase before commercial batches can be produced.Role Description
The Process Technologies and Projects team plays a key role in process implementation and production support. They ensure that new products or process changes are handed over to the operations team on-time, with the associated documentation and where needed the required hardware and software changes.Responsibilities
- Manage global, regional and local infrastructure projects with varying levels of complexity- Specify project requests, taking into account guidelines and procedures
– Group, prioritize and optimize those requests
- Take responsibility for gathering project requirements, define/document solutions and associated cost pictures
- Responsible for assembling project teams, identifying appropriate resources needed, develop and execute project plans, and assign individual responsibilities
- Function as a team builder for projects managed
- Track, schedule and manage issues to ensure NCS commitment dates and project deliverables are met
- Deliver projects within requested timeframe and budget
Requirements
- Bachelor Degree in Mathematics, Engineering, Computer Science OR equivalent through experience.- Must have minimum 5 years Project Management experience (budgets, plan, schedule, issue tracking/remediation, risk analysis, etc.)
- At least 2 years experience managing and performing Technical Support Services contracts or tasks
- Must have GEP / GMP knowledge related to system modification/ introduction in a running GMP facility.
- Beneficial: Computer infrastructure operations or deployment background
- Beneficial: Technical writing skills to write the proper documentation according to internal regulations (FDA part 11, GxP, etc.)
Other information
Submit your application before the 9th of SeptemberAre you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
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