QC Specialist
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Søborg
Ferrosan Medical Devices A/S, Søborg is looking for highly professional, committed and motivated QC Specialist, who can contribute to ensure the quality of our hemostatic products.
Your role
The QC laboratory is responsible for analysis of raw materials, components, intermediates and finished products. Most of the analyses performed are microbiological and physical tests. The analytical results form basis for the final release of our medical devices and combination products to the market. Consequently we work according to GMP and ISO 13485. QC also holds the responsibility for external sterilization processes (γ- and e-beam-irradiation and ethylene oxide), environmental monitoring of production areas and stability studies.
As a QC specialist you will together with your QC colleagues be responsible for analytical methods used in QC, have regular contact to our external partners and support our on-site production in quality and microbiological issues. Further you will participate in projects optimizing manufacturing processes and developing new products.
Among versatile tasks you are responsible for:
Your profile
We are looking for a committed, motivated, positive and highly quality minded person. In order to succeed in the job it is required that you are flexible, pragmatic, structured, able to prioritize and manage multiple task within deadlines. You are responsible and work independent in a dynamic and challenging environment. You are able to make fast decisions, communicate clearly and have good interpersonal skills. You thrive on working with a combination of projects and routine tasks related to manufacturing of medical devices.
Qualifications
Working at Ferrosan Medical Devices
Ferrosan Medical Devices A/S is driven by a dedicated energetic organization with impressive growth. Our company has 200 employees covering all aspects of tasks related to development and production of medical devices and combination products. In daily work you will collaborate with colleagues throughout the company involved in production flow from receipt of raw materials to release of finished products. LEAN principles are implemented in the way we work. We offer an interesting and challenging job in a growing company. The position is new and will have reference to the QC Manager. You will join a QC team of 3 specialists and 5 technicians.
Deadline
Please submit your application including CV no later than 4th of February via link. Submit in Danish or English no preference. Review of applications will be conducted on an on-going basis. If you have any questions regarding the position, please do not hesitate to contact QC Manager Lise Moesby (2544 8307).
Ferrosan Medical Devices A/S Biomaterials develops and manufactures absorbable gelatin products and combination products for haemostatic use during surgery. The products are marketed and distributed in more than 100 countries by our partner Ethicon Biosurgery, a part of Johnson&Johnson. We are 200 employees located in Søborg. www.ferrosanmedicaldevices.com
Your role
The QC laboratory is responsible for analysis of raw materials, components, intermediates and finished products. Most of the analyses performed are microbiological and physical tests. The analytical results form basis for the final release of our medical devices and combination products to the market. Consequently we work according to GMP and ISO 13485. QC also holds the responsibility for external sterilization processes (γ- and e-beam-irradiation and ethylene oxide), environmental monitoring of production areas and stability studies.
As a QC specialist you will together with your QC colleagues be responsible for analytical methods used in QC, have regular contact to our external partners and support our on-site production in quality and microbiological issues. Further you will participate in projects optimizing manufacturing processes and developing new products.
Among versatile tasks you are responsible for:
- Validation of analytical methods and implementing of new methods in QC
- Analytical methods and equipment in QC
- Prepare qualification and validation documents for analytical equipment and methods
- Contact to external collaborators and participate in audits
- Guidance and support of QC technicians
- Handling deviations and CAPAs
- Prepare and maintain documents and instructions in the quality management system
Your profile
We are looking for a committed, motivated, positive and highly quality minded person. In order to succeed in the job it is required that you are flexible, pragmatic, structured, able to prioritize and manage multiple task within deadlines. You are responsible and work independent in a dynamic and challenging environment. You are able to make fast decisions, communicate clearly and have good interpersonal skills. You thrive on working with a combination of projects and routine tasks related to manufacturing of medical devices.
Qualifications
- Relevant academic background (Master degree or PhD) within life sciences (pharmacy, chemistry, human biology)
- At least 3 years practical experience from QC laboratory
- Solid experience with microbial test methods and other testing of sterile medical devices
- Strong knowledge of microbiological challenges and issues related to production of sterile products
- Experience with stability studies
- Flair for IT. Knowledge of SAP is an advantage
- Proficiency in Danish and English
Working at Ferrosan Medical Devices
Ferrosan Medical Devices A/S is driven by a dedicated energetic organization with impressive growth. Our company has 200 employees covering all aspects of tasks related to development and production of medical devices and combination products. In daily work you will collaborate with colleagues throughout the company involved in production flow from receipt of raw materials to release of finished products. LEAN principles are implemented in the way we work. We offer an interesting and challenging job in a growing company. The position is new and will have reference to the QC Manager. You will join a QC team of 3 specialists and 5 technicians.
Deadline
Please submit your application including CV no later than 4th of February via link. Submit in Danish or English no preference. Review of applications will be conducted on an on-going basis. If you have any questions regarding the position, please do not hesitate to contact QC Manager Lise Moesby (2544 8307).
Ferrosan Medical Devices A/S Biomaterials develops and manufactures absorbable gelatin products and combination products for haemostatic use during surgery. The products are marketed and distributed in more than 100 countries by our partner Ethicon Biosurgery, a part of Johnson&Johnson. We are 200 employees located in Søborg. www.ferrosanmedicaldevices.com
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 15.1.2020, 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.
- Øvrige
- Søborg
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