Laboratory System Manager
- Research & Development
- Denmark - Måløv
Would you like to become the System Manager responsible for laboratory computerised instruments such as ELISA readers coupled to validated software? And would you like to further develop your expertise in validation of computerised laboratory systems? If so, you could be our new colleague in Quality & Systems Management.
About the department
Located in Måløv, Quality & Systems Management is part of Non-clinical Development and we work in a regulated area (GLP and GCP). The systems management group supports laboratory computer systems as well as data management systems with regards to system administration, system upgrades, platform upgrades, accompanying change control as well as troubleshooting of system issues.
The job
Your main focus will be split between System Manager tasks for our ELISA readers coupled to Magellan software and specialist tasks regarding implementation and validation of a wide variety of computerised laboratory systems. This will include working in accordance with Novo Nordisk procedures and external guidelines for Computer Systems Validation (e.g. GAMP).
As System Manager you will on a daily basis be working with technicians and academics related to the use and maintenance of ELISA readers and Magellan software. You will support users in Bioanalysis and Antibody Analysis departments and handle reported incidents and errors. Updates of system related procedures, user administration, vendor services, periodic reviews and planning of system corrections/updates will also be part of the System Manager tasks.
As a computer system validation specialist you will take part in small project groups, and you will be driving implementation of new computerised laboratory systems typically consisting of 1-2 computers and associated apparatus according to the V-model, i.e. determine the validation process, help define user requirements and ensure appropriate test protocols and documentation
Qualifications
You have a BSc or MSc within natural sciences or other relevant degree and experience from lab work with ELISA-related software and qualification of computerised systems in a regulated area. We are a friendly group looking for someone with an open and analytical personality, who is flexible and positive towards the challenges which this position will bring and determined not to compromise on quality.
You may have experience from GMP, QC laboratories, IT system management, LIMS or laboratory automation and are eager to apply your skills to a new area.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Applications are welcome in both Danish and English.
Contact
For further information, please contact Gitte Konradsen on +45 3075 8303.
Deadline
7 August 2013.
- Research & Development
- Denmark - Måløv
Would you like to become the System Manager responsible for laboratory computerised instruments such as ELISA readers coupled to validated software? And would you like to further develop your expertise in validation of computerised laboratory systems? If so, you could be our new colleague in Quality & Systems Management.
About the department
Located in Måløv, Quality & Systems Management is part of Non-clinical Development and we work in a regulated area (GLP and GCP). The systems management group supports laboratory computer systems as well as data management systems with regards to system administration, system upgrades, platform upgrades, accompanying change control as well as troubleshooting of system issues.
The job
Your main focus will be split between System Manager tasks for our ELISA readers coupled to Magellan software and specialist tasks regarding implementation and validation of a wide variety of computerised laboratory systems. This will include working in accordance with Novo Nordisk procedures and external guidelines for Computer Systems Validation (e.g. GAMP).
As System Manager you will on a daily basis be working with technicians and academics related to the use and maintenance of ELISA readers and Magellan software. You will support users in Bioanalysis and Antibody Analysis departments and handle reported incidents and errors. Updates of system related procedures, user administration, vendor services, periodic reviews and planning of system corrections/updates will also be part of the System Manager tasks.
As a computer system validation specialist you will take part in small project groups, and you will be driving implementation of new computerised laboratory systems typically consisting of 1-2 computers and associated apparatus according to the V-model, i.e. determine the validation process, help define user requirements and ensure appropriate test protocols and documentation
Qualifications
You have a BSc or MSc within natural sciences or other relevant degree and experience from lab work with ELISA-related software and qualification of computerised systems in a regulated area. We are a friendly group looking for someone with an open and analytical personality, who is flexible and positive towards the challenges which this position will bring and determined not to compromise on quality.
You may have experience from GMP, QC laboratories, IT system management, LIMS or laboratory automation and are eager to apply your skills to a new area.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Applications are welcome in both Danish and English.
Contact
For further information, please contact Gitte Konradsen on +45 3075 8303.
Deadline
7 August 2013.