Associate Scientist
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 organisation, based in Zuid-Holland Netherlands.
- Accurately completion of documentation such as batch records, logbooks, etc.
- Working precisely, detecting and solving acute problems and communicate possible abnormalities.
- Actively participating in setting up documentation to ensure successful production runs.
- Responsible as area owner that the production areas are according EHSS and compliance standards.
- Internal organization of the facility, including ISL, 5S and kanban systems.
- Involvement in deviation investigation and follow up.
- Write training documentation and perform training of new operators.
- Connects with warehouse
- Interacts with stakeholders and customer at Operations and QA
- Connects with the Preparation, Downstream and support team
- 2-6 years’ experience in a biotechnology or biopharmaceutical industry environment.
- GMP experience, either in the pharma or medical device sector
- English; speaking, writing, and verbal skills are fluent (Dutch is a plus but not required)
- Able to set priorities
- Quality, efficiency, accuracy and reliability of work
- Planning, adherence to timelines
- Innovating capabilities
- Communication capabilities
- Quality of SOP's
- Personal targets
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Helene de Vries.
The Company
In the organization, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to the company.Role Description
As an Associate Scientist DSO you will be responsible for conducting research in assigned areas under direct supervision using established methodology.Responsibilities
- Taking part in activities related to the production of cGMP batches. This includes processes such as batch record review and taking escalations from cell and virus culture, purification processes, formulation & fill and in-process testing.- Accurately completion of documentation such as batch records, logbooks, etc.
- Working precisely, detecting and solving acute problems and communicate possible abnormalities.
- Actively participating in setting up documentation to ensure successful production runs.
- Responsible as area owner that the production areas are according EHSS and compliance standards.
- Internal organization of the facility, including ISL, 5S and kanban systems.
- Involvement in deviation investigation and follow up.
- Write training documentation and perform training of new operators.
- Connects with warehouse
- Interacts with stakeholders and customer at Operations and QA
- Connects with the Preparation, Downstream and support team
Requirements
- Bachelor or Master level or equivalent- 2-6 years’ experience in a biotechnology or biopharmaceutical industry environment.
- GMP experience, either in the pharma or medical device sector
- English; speaking, writing, and verbal skills are fluent (Dutch is a plus but not required)
- Able to set priorities
- Quality, efficiency, accuracy and reliability of work
- Planning, adherence to timelines
- Innovating capabilities
- Communication capabilities
- Quality of SOP's
- Personal targets
Other information
The company prefers a full time candidate but is open to discuss 32 hours. This is not a hands-on position, however you will be visiting production and support the operators.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Helene de Vries.
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