Manufacturing Associates (Process Operators) to support the expansion project at Fujifilm Diosynth Biotechnologies
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Hillerød
For the Drug Substance Manufacturing Unit in Hillerød, Fujifilm Diosynth Biotechnologies is looking for Manufacturing Associates (Process Operators) to support the expansion project.
FUJIFILM Diosynth Biotechnologies is currently expanding its capacity to support the large-scale production by adding 14 x 20,000L bioreactors and three downstream processing lines in Hillerød. The additional production capacity will make the facility the largest end-to-end Contract Development and Manufacturing Organization (CDMO) in Europe, offering a total of 20 x 20,000L bioreactors for drug substance production complemented by comprehensive drug product and finished goods services.
This is an excellent opportunity to join our company at a pivotal time of growth and be part of an exciting journey.
We are currently looking for candidates to support the expansion with the Commissioning Readiness of all Systems, to support Equipment Start-up and IOQ Testing. As well as performing the PQ in close collaboration with validation, executing water batches and technical batches with engineering. This is an excellent opportunity to get extensive knowledge on the manufacturing equipment before we go into production in 2024.
When the project is finished you will automatically be offered a job opportunity in two places. To continue with the next expansion project on site and carry along your learnings or our new Drug Substance Manufacturing department covering - respectively – Upstream & Downstream. The two departments cover different steps in the biopharmaceutical production such as Media Preparation, CIP & SIP of equipment, growth of cell cultures, and purification via multiple column steps.
During the time in the project,you will work either fixed day or fixed evening, 7 days during a 14-day period, including every other weekend.Please add in your application which shift or shifts you prefer.
The work schedule is as follows:
Week 1: Monday, Tuesday, Friday, Saturday, and Sunday
Week 2: Wednesday and Thursday
The shifts are as follows:
Day: 06:00 – 17:04
Evening: 13:00 – 23:13
Tasks
Qualifications
We are looking for process operators, preferable with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their bachelor’s or master’s degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.
It is a plus if you have experience with cGMP and/or SOPs or knowledge of chromatography and filtration processes.
You will get the opportunity to customize your development plan in agreement with your manager based on your wishes and qualifications.
We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools. You are very quality-oriented and thorough. You are proactive, responsible, organized and able to take ownership of tasks. Furthermore, you are a good team player who thrives on setting a good example.
You must be keen on learning new things, and the first period will of course include thorough training.
Your application
Has the above sparked your interest? Then we look forward to receiving your CV and hearing about your motivation for the position as soon as possible. We are inviting for interviews on an ongoing basis, as the start date is as soon as possible.
FUJIFILM Diosynth Biotechnologies is currently expanding its capacity to support the large-scale production by adding 14 x 20,000L bioreactors and three downstream processing lines in Hillerød. The additional production capacity will make the facility the largest end-to-end Contract Development and Manufacturing Organization (CDMO) in Europe, offering a total of 20 x 20,000L bioreactors for drug substance production complemented by comprehensive drug product and finished goods services.
This is an excellent opportunity to join our company at a pivotal time of growth and be part of an exciting journey.
We are currently looking for candidates to support the expansion with the Commissioning Readiness of all Systems, to support Equipment Start-up and IOQ Testing. As well as performing the PQ in close collaboration with validation, executing water batches and technical batches with engineering. This is an excellent opportunity to get extensive knowledge on the manufacturing equipment before we go into production in 2024.
When the project is finished you will automatically be offered a job opportunity in two places. To continue with the next expansion project on site and carry along your learnings or our new Drug Substance Manufacturing department covering - respectively – Upstream & Downstream. The two departments cover different steps in the biopharmaceutical production such as Media Preparation, CIP & SIP of equipment, growth of cell cultures, and purification via multiple column steps.
During the time in the project,you will work either fixed day or fixed evening, 7 days during a 14-day period, including every other weekend.Please add in your application which shift or shifts you prefer.
The work schedule is as follows:
Week 1: Monday, Tuesday, Friday, Saturday, and Sunday
Week 2: Wednesday and Thursday
The shifts are as follows:
Day: 06:00 – 17:04
Evening: 13:00 – 23:13
Tasks
- Support and review design deliverables incl. drawings, data sheets, specifications and engineering lists.
- Perform field walk-downs and participate actively in daily/weekly/monthly meetings and ensure timely updates
- Equipment preparation and testing
- Reviewing Protocols and Work instructions
- Executing PQ Protocols guided by work instructions
- Trouble shooting
Qualifications
We are looking for process operators, preferable with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their bachelor’s or master’s degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.
It is a plus if you have experience with cGMP and/or SOPs or knowledge of chromatography and filtration processes.
You will get the opportunity to customize your development plan in agreement with your manager based on your wishes and qualifications.
We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools. You are very quality-oriented and thorough. You are proactive, responsible, organized and able to take ownership of tasks. Furthermore, you are a good team player who thrives on setting a good example.
You must be keen on learning new things, and the first period will of course include thorough training.
Your application
Has the above sparked your interest? Then we look forward to receiving your CV and hearing about your motivation for the position as soon as possible. We are inviting for interviews on an ongoing basis, as the start date is as soon as possible.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Hillerød.
Jobbet er oprettet på vores service den 23.3.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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