At Genmab, we are dedicated to building extra not ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.Does this inspire you and feel like a fit? Then we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring integrity, consistency and adherence to standards of data and produces well-structured, high quality data summaries in tables, figures and listings for decision making.Responsibilities in leading the programming efforts of at least one study are in scope. The Programming Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by developing and writing corresponding SAS or other programs. Responsibilities/tasks - including but not limited to: Reviews CRFs for adequacy and consistency Supports the establishment and maintenance of Genmab SDTM and ADaM database standards Performs database standards consistency checks on databases delivered by the preferred DM & Statistics vendor to Genmab Produces other in-house checks of data consistencies Supports specification and pooling of data across clinical trials within the same projectSupports in-house production of analysis datasets, tables, figures and listings, by writing the corresponding programs and ensuring QC before formal release, for the following non-comprehensive list of deliverables: IB, DSUR, briefing packages for FDA, EMA etc., supplementary in-house preparations for DMC-meetings, RP2D- selection preparations, supplementary material for interim analysis and final analyses (e.g. sub-group or other analyses not pre-defined in the SAP), answers to questions posed by regulatory authorities or ethics committees, answers to in-house questions related to data quality, safety monitoring, medical questions etc. Performs sponsor oversight of programming activities on the DM & Statistics vendor Performs QC on SAS-code written by other Genmab colleagues Supports submissions by ensuring that the programming-related part of the file is consistent with current electronic submission standards and guidelines. Supports development of GenSense Dashboards by providing guidance on data structure, organization, and contents of the Genmab SDTM-databases to the Dashboard-developers and programmers. Supports resource planning and outsourcing of programming activities. Supports developing and reviewing standard processes and templates. Contributes to knowledge sharing, skill building and good collaboration with stakeholders and colleagues Contributes to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge Contributes to process improvements Maintains up-to-date knowledge and competencies within relevant therapeutic and professional areas Maintains up-to-date knowledge on relevant regulatory guidelines/requirements Maintains a good working relationship with stakeholders and colleagues Participates and represent programming in teams and meetings Requirements:Minimum BSc. or equivalent qualifications At least 2-5 years of experience within the pharmaceutical industryHas experience working in a global context Proficient in both written and spoken English Has experience with the SAS software package Additional Job DescriptionAssist with consistency checks against standards including checks on databases delivered by vendors, and provide sponsor oversight of vendor programming activitiesExecute assigned tasks for in-house production of analysis datasets, tables, figures and listings as well as specification and pooling of data across clinical trials within assigned projectsAssist with QC on SAS-code written by other Genmab colleaguesExecute activities related to development of GenSense Dashboards with some guidance on data structure, organization, and contents of the Genmab SDTM-databasesAssist with optimization of programming processes, standards, and templatesAbout YouYou are genuinely passionate about our purposeYou bring precision and excellence to all that you doYou believe in our rooted-in-science approach to problem-solvingYou are a generous collaborator who can work in teams with a broad spectrum of backgroundsYou take pride in enabling the best work of others on the teamYou can grapple with the unknown and be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and are not afraid to have a little fun while you do so!LocationsGenmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.About GenmabGenmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO ) antibody medicines.Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit and follow us on LinkedIn and X .Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice () .
At Genmab, we are dedicated to building extra not ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.Does this inspire you and feel like a fit? Then we would love to have you join us!
The RoleThe Senior Associate, Facility Operations is a hands-on role focused on keeping our Soft Services everyday operations running smoothly. You will be directly involved in managing our facilities, handling logistical needs (for events), and ensuring that our administrative processes work seamlessly for our teams. This position requires excellent organization, the ability to solve problems independently, and strong collaboration skills, as you will be working with many of our internal departments and external partners. Your practical approach and clear communication are exactly what we need in this role!
Please note that this is a full-time, onsite role where you will be at the heart of our day-to-day operations driving essential improvements that directly support our mission to develop knock-your-socks-off medicines for cancer patients!ResponsibilitiesServe as the main contact for office and site-related needs, including coworking/flex-office spaces.Lead space planning efforts, optimize layouts, and maintain accurate records.Oversee local reception services by improving service levels, enhancing amenities, and training new team members.Coordinate governance, departmental, and project meetings by scheduling, managing logistics (in-person and virtual), drafting agendas, taking minutes, and tracking action items.Work with global colleagues to support international meeting coordination and on-site event organization, including engagement activities and space setup.Streamline administrative processes by managing MS SharePoint, Teams, Smartsheets, and other electronic databases; track deadlines and follow-ups.Update and maintain organizational data such as site lists, org charts, and headcount trackers.Coordinate domestic and international travel logistics for Facilities leadership, including visa, lodging, transportation, and itineraries.Manage purchase requisitions, orders through SAP, expense reports via Concur, and support financial processes with the global Facilities Management team.Collaborate with Legal, Finance, and Procurement on contracts, approvals, and document archiving.Train new Facilities team members and lead onboarding; participate in ad-hoc local and global projects.RequirementsBachelor's degree (HBO level) or equivalent experience.At least 3 years of experience in facility operations or a related field, preferably in biotech/pharma environment. Strong communication skills in both Dutch and English.Excellent organizational, time management, and multi-priority handling skills.Strong problem-solving and decision-making abilities.Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel, Teams, SharePoint) and IT systems such as Smartsheet; experience with SAP and Concur is a plus.Effective communication and collaboration skills for working with global teams.Prior experience in biotech/pharma or a related industry is preferred.Willingness to travel 10-15% as required. About YouYou are genuinely passionate about our purposeYou bring precision and excellence to all that you doYou believe in our rooted-in-science approach to problem-solvingYou are a generous collaborator who can work in teams with a broad spectrum of backgroundsYou take pride in enabling the best work of others on the teamYou can grapple with the unknown and be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and are not afraid to have a little fun while you do so!LocationsGenmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.About GenmabGenmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO ) antibody medicines.Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit and follow us on LinkedIn and X .Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice () .Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract.
At Genmab, we are dedicated to building extra not ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.Does this inspire you and feel like a fit? Then we would love to have you join us!
The Role
We are seeking a dedicated Lab Safety Manager to join our QM & Lab Compliance department, where you will play a key role in overseeing and enhancing the safety culture in our Utrecht laboratories. In this role, you are responsible for developing and enforcing Occupational Health & Safety (OHS) policies, ensuring compliance with all applicable Dutch laws and regulations, and integrating chemical safety best practices into our internal procedures. Are you a proactive leader, do you foster a safe working environment through risk assessments, education, training, inspections, and regulatory compliance? Then we want to hear from you!In addition to the Lab Safety Manager responsibilities, this role also includes serving as the Chemical Safety Officer (CSO). As CSO, the individual will be responsible for coordinating chemical safety policies, conducting internal inspections, supporting external inspections, and ensuring compliance with chemical hygiene and hazardous materials regulations.This position is a critical part of the QM & Lab Compliance department, ensuring alignment between safety policies, compliance standards, and operational excellence at Genmab, Netherlands.
ResponsibilitiesLab Safety ManagementDevelop, ensure implementation, and maintain OHS policies and programs specific to laboratory environments.Advise and educate staff on various safety-related topics, including safe equipment use, and chemical handling.Conduct risk assessments and ensure preventive measures are taken for laboratory operations.Initiate and organize OHS training programs for laboratory employees to promote safety awareness.Inspect laboratory premises and monitor personnel activities to identify safety issues or non-conformities.
Chemical Safety Officer (CSO) ResponsibilitiesOversee and coordinate the laboratory Chemical Safety Policy, including chemical hygiene, internal inspections, and chemical inventory management.Investigate and analyze chemical-related accidents and incidents, implementing corrective actions.Provide expertise and guidance for hazardous materials clean-up and chemical safety training.Ensure compliance with chemical safety regulations, including the proper storage, handling, and disposal of hazardous substances.
Regulatory ComplianceTranslate all applicable Dutch laws and regulations into internal safety procedures and processes applied in the labs.Ensure continuous alignment of laboratory safety policies with national and international regulatory standards.Maintain documentation and reporting mechanisms to demonstrate compliance with legal and corporate safety requirements.
Requirements
Background in Occupational Health & Safety, Chemical Engineering, Environmental Science, or a related field. P reference of being certified as "Arbeidshygienist".Prior experience in a supervisory role and team management.Experience in lab safety management, chemical safety, or a related safety leadership role.Strong knowledge of OHS regulations, chemical safety standards, and hazardous materials management.Experience in risk assessments, accident investigations, and safety audits.Ability to develop and deliver safety training programs for laboratory personnel.Strong problem-solving and decision-making skills with a proactive approach to safety improvements.Excellent communication skills and ability to engage with diverse stakeholders across R&D.Ability to be proactive, enthusiastic, and goal orientated.A team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders (e.g. Scientists, Trial Managers, Data Managers, Clinicians, vendors labs). About YouYou are genuinely passionate about our purposeYou bring precision and excellence to all that you doYou believe in our rooted-in-science approach to problem-solvingYou are a generous collaborator who can work in teams with a broad spectrum of backgroundsYou take pride in enabling the best work of others on the teamYou can grapple with the unknown and be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and are not afraid to have a little fun while you do so!LocationsGenmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.About GenmabGenmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO ) antibody medicines.Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit and follow us on LinkedIn and X .Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice () .Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract.
At Genmab, we are dedicated to building extra not ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.Does this inspire you and feel like a fit? Then we would love to have you join us!
The RoleThe Senior Associate, Facility Operations is a hands-on role focused on keeping our Soft Services everyday operations running smoothly. You will be directly involved in managing our facilities, handling logistical needs (for events), and ensuring that our administrative processes work seamlessly for our teams. This position requires excellent organization, the ability to solve problems independently, and strong collaboration skills, as you will be working with many of our internal departments and external partners. Your practical approach and clear communication are exactly what we need in this role!
Please note that this is a full-time, onsite role where you will be at the heart of our day-to-day operations driving essential improvements that directly support our mission to develop knock-your-socks-off medicines for cancer patients!ResponsibilitiesServe as the main contact for office and site-related needs, including coworking/flex-office spaces.Lead space planning efforts, optimize layouts, and maintain accurate records.Oversee local reception services by improving service levels, enhancing amenities, and training new team members.Coordinate governance, departmental, and project meetings by scheduling, managing logistics (in-person and virtual), drafting agendas, taking minutes, and tracking action items.Work with global colleagues to support international meeting coordination and on-site event organization, including engagement activities and space setup.Streamline administrative processes by managing MS SharePoint, Teams, Smartsheets, and other electronic databases; track deadlines and follow-ups.Update and maintain organizational data such as site lists, org charts, and headcount trackers.Coordinate domestic and international travel logistics for Facilities leadership, including visa, lodging, transportation, and itineraries.Manage purchase requisitions, orders through SAP, expense reports via Concur, and support financial processes with the global Facilities Management team.Collaborate with Legal, Finance, and Procurement on contracts, approvals, and document archiving.Train new Facilities team members and lead onboarding; participate in ad-hoc local and global projects.RequirementsBachelor's degree (HBO level) or equivalent experience.At least 3 years of experience in facility operations or a related field, preferably in biotech/pharma environment. Strong communication skills in both Dutch and English.Excellent organizational, time management, and multi-priority handling skills.Strong problem-solving and decision-making abilities.Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel, Teams, SharePoint) and IT systems such as Smartsheet; experience with SAP and Concur is a plus.Effective communication and collaboration skills for working with global teams.Prior experience in biotech/pharma or a related industry is preferred.Willingness to travel 10-15% as required. About YouYou are genuinely passionate about our purposeYou bring precision and excellence to all that you doYou believe in our rooted-in-science approach to problem-solvingYou are a generous collaborator who can work in teams with a broad spectrum of backgroundsYou take pride in enabling the best work of others on the teamYou can grapple with the unknown and be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and are not afraid to have a little fun while you do so!LocationsGenmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.About GenmabGenmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO ) antibody medicines.Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit and follow us on LinkedIn and X .Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice () .Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract.
At Genmab, we are dedicated to building extra not ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.Does this inspire you and feel like a fit? Then we would love to have you join us!
The Role
We are seeking a dedicated Lab Safety Manager to join our QM & Lab Compliance department, where you will play a key role in overseeing and enhancing the safety culture in our Utrecht laboratories. In this role, you are responsible for developing and enforcing Occupational Health & Safety (OHS) policies, ensuring compliance with all applicable Dutch laws and regulations, and integrating chemical safety best practices into our internal procedures. Are you a proactive leader, do you foster a safe working environment through risk assessments, education, training, inspections, and regulatory compliance? Then we want to hear from you!In addition to the Lab Safety Manager responsibilities, this role also includes serving as the Chemical Safety Officer (CSO). As CSO, the individual will be responsible for coordinating chemical safety policies, conducting internal inspections, supporting external inspections, and ensuring compliance with chemical hygiene and hazardous materials regulations.This position is a critical part of the QM & Lab Compliance department, ensuring alignment between safety policies, compliance standards, and operational excellence at Genmab, Netherlands.
ResponsibilitiesLab Safety ManagementDevelop, ensure implementation, and maintain OHS policies and programs specific to laboratory environments.Advise and educate staff on various safety-related topics, including safe equipment use, and chemical handling.Conduct risk assessments and ensure preventive measures are taken for laboratory operations.Initiate and organize OHS training programs for laboratory employees to promote safety awareness.Inspect laboratory premises and monitor personnel activities to identify safety issues or non-conformities.
Chemical Safety Officer (CSO) ResponsibilitiesOversee and coordinate the laboratory Chemical Safety Policy, including chemical hygiene, internal inspections, and chemical inventory management.Investigate and analyze chemical-related accidents and incidents, implementing corrective actions.Provide expertise and guidance for hazardous materials clean-up and chemical safety training.Ensure compliance with chemical safety regulations, including the proper storage, handling, and disposal of hazardous substances.
Regulatory ComplianceTranslate all applicable Dutch laws and regulations into internal safety procedures and processes applied in the labs.Ensure continuous alignment of laboratory safety policies with national and international regulatory standards.Maintain documentation and reporting mechanisms to demonstrate compliance with legal and corporate safety requirements.
Requirements
Background in Occupational Health & Safety, Chemical Engineering, Environmental Science, or a related field. P reference of being certified as "Arbeidshygienist".Prior experience in a supervisory role and team management.Experience in lab safety management, chemical safety, or a related safety leadership role.Strong knowledge of OHS regulations, chemical safety standards, and hazardous materials management.Experience in risk assessments, accident investigations, and safety audits.Ability to develop and deliver safety training programs for laboratory personnel.Strong problem-solving and decision-making skills with a proactive approach to safety improvements.Excellent communication skills and ability to engage with diverse stakeholders across R&D.Ability to be proactive, enthusiastic, and goal orientated.A team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders (e.g. Scientists, Trial Managers, Data Managers, Clinicians, vendors labs). About YouYou are genuinely passionate about our purposeYou bring precision and excellence to all that you doYou believe in our rooted-in-science approach to problem-solvingYou are a generous collaborator who can work in teams with a broad spectrum of backgroundsYou take pride in enabling the best work of others on the teamYou can grapple with the unknown and be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and are not afraid to have a little fun while you do so!LocationsGenmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you're in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.About GenmabGenmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO ) antibody medicines.Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit and follow us on LinkedIn and X .Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice () .Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract.
