Home › Companies › Hcjy Fa Us2 Oraclecloud Com CX 1 › Principal Regulatory Affairs Specialist - EMEA (Cluster Partner)
Principal Regulatory Affairs Specialist - EMEA (Cluster Partner)
Hcjy Fa Us2 Oraclecloud Com CX 1 · NL-Gorinchem, Gorinchem, NL · On Site · Active · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Hcjy Fa Us2 Oraclecloud Com CX 1 |
| Title | Principal Regulatory Affairs Specialist - EMEA (Cluster Partner) |
| Normalized title | - |
| Department / team | Compliance, Risk & Legal |
| Location | Gorinchem, NL, Canada |
| Work model | On Site |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-04-14 / 2026-05-31 |
| Changed / last seen | 2026-05-31 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Hcjy Fa Us2 Oraclecloud Com CX 1. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Gorinchem. | Open |
| Department jobs | Active postings in Compliance, Risk & Legal. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Hcjy Fa Us2 Oraclecloud Com CX 1 |
| Source | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
Job title: Principal Regulatory Affairs Specialist - EMEA
Department: Regulatory Affairs
Location: Southampton, UK / Gorinchem, Netherlands or Gothenburg, Sweden
GLS: P04
Working hours: UK – 37.5 hours per week, Netherlands or Sweden – 40 hours per week
A brighter future awaits you
What to expect:
The Principal Regulatory Affairs Specialist will provide expert level regulatory support and direction across our UK&I, BeNeLux and Nordic Clusters, for products from concept to launch, and beyond into post market, as well as regulatory processes. The Principal RA Specialist articulates and executes the agreed regulatory strategy for assigned corporate projects. Leads the creation, development, and implementation of global/regional regulatory affairs procedures for marketed products and to maintain, update or remediate company’s regulatory compliance status.
Essential Functions & Accountabilities:
Registration Activity
Reviews and approves regulatory documents for the registration of current and new products in assigned markets.
Oversees the maintenance of submission documents, and agile databases in an accurate, complete and timely manner to ensure prompt and accurate access to company regulatory information.
Maintains, updates and remediates regulatory files and documents as required. This includes maintaining communication across the EMEA RA team and other departments, sites, or business units, to provide regulatory status reports.
Coaches/Mentors more junior team members with submission
Monitoring Registration Requirements within Region
Maintains up-to-date knowledge of regional and national regulations, guidelines, and advisory documents required for marketing CooperVision products in a specified region.
Communicates applicable regulatory requirements to CooperVision Regulatory Affairs management and business partners.
Analyses impact and communicate to management changes in regulations or requirements that have been identified.
Establish and leverage working relationships with government, regulatory agencies, and trade associations for the purpose of advocating CooperVision positions
Technical Documentation
Reviews compiled Technical Files for CE approval prior to submission
Supports RA Management with Notified Body requests for information.
As required, plays a significant role in technical audits in the UK, EU, ACE and MENA region, i.e. preparation, contingency planning, response, findings and close out activities.
Support to CooperVision Processes
Represents the perspective of regulatory affairs to the company.
Interprets general business objectives and effectively present information to manager and regions.
Reviews and approves product labelling. Initiates IFUs and other required product labelling in line with relevant UK, EU, ACE & MENA requirements.
Supports “Own Brand” and “Private label “customers and liaises with EU Competent Authorities and other Ministries of health as necessary
Provides input to Regulatory Affairs Impact Documents (RAIDS) from UK EU, ACE & MENA perspective.
Undertakes other administrative tasks to support CE marking and regional registrations.
Responsible for exhibiting professional behaviour with internal and external business associates that reflect positively on CooperVision, The individual conveys a trustworthy, credible, and reliable image at all times.
Act as a resource to the regions on quality issues and propose changes to minimise risks and enhance quality, reliability, safety and productivity.
Act as spokesperson, when appropriate, regarding CooperVision practices, public policy, business interests; arrange for technical explanations from internal or external experts.
Support RA compliance activities as necessary in assigned regions
Independently manage multiple projects, department initiatives and day to day tasks
About you:
Experience:
6-8 years of medical device regulatory experience. Technical writing experience. Has experience evaluating manufacturing changes for impact on global regulatory affairs submissions. Medical device industry experiences including strong working knowledge and experience with MDD and MDR. Ability to operate in a business-driven model providing quick, salient analysis and concrete action plans emphasis on understanding and anticipating business needs and interests and devising proactive approaches/responses. Must have the ability to build relationships and influence decision makers. Comprehension of industry developments and changes in the political environment. Extensive network-building and contact experience. Capability to interact effectively and credibly at senior levels. Experience in electronic document management systems Strong IT skills, problem solving ability, analytical and communication skills.
Knowledge, Skills and Abilities:
Understanding of ISO 13485 requirements and EU medical device regulations. Ability to read and understand technical material. Excellent attention to detail Excellent organizational skills Excellent written and verbal communication skills. Excellent organizational skills. Computer literate, with intermediate skill in the use of Word, Excel and Outlook, and some knowledge of relational database systems, e.g. Agile Project Management system. Ability to work effectively either alone or as part of a team. Managing time effectively and completing tasks on time with general supervision. Experienced at reviewing and approving product labelling. Flexible and able to self-manage multiple priorities. Able to work effectively in multinational/multicultural environments. Flexibility to work across the UK sites Full, current driving license
What we offer:
You’ll receive competitive compensation and a fantastic benefits package.
We are committed to our employees’ personal and professional development and offer extensive training to support your career growth and help every individual to reach their full potential. To help us achieve our goals, we’ll give you everything you need to help you achieve yours.
We also provide access to LinkedIn Learning to help you develop in you career and grow with CooperVision.
If you like what you see, take the first step towards your Brighter Future and apply today! All suitably qualified applicants will receive equal consideration and opportunities from CooperVision.
# ONSITE
#LI-JS1
Full job record
| Job ID | ee18c6934aa8d1555c4cc3b190df6b8147062994 |
| Org ID | fd5c005d-2102-408b-80a5-9404893f9b97 |
| Source ID | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| Board ID | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| Provider | oracle_hcm |
| Provider Job Key | 10823 |
| Title | Principal Regulatory Affairs Specialist - EMEA (Cluster Partner) |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | NL-Gorinchem, Gorinchem, NL |
| Department | Compliance, Risk & Legal |
| Team | — |
| Employment Type | full_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | Canada |
| Region | NL |
| City | Gorinchem |
| Salary Raw | Description Job title: Principal Regulatory Affairs Specialist - EMEA Department: Regulatory Affairs Location: Southampton, UK / Gorinchem, Netherlands or Gothenburg, Sweden GLS: P04 Working hours: UK – 37.5 hours per week, Netherlands or Sweden – 40 hours per week A brighter future awaits you What to expect: The Principal Regulatory Affairs Specialist will provide expert level regulatory support and direction across our UK&I, BeNeLux and Nordic Clusters, for products from concept to launch, and beyond into post market, as well as regulatory processes. The Principal RA Specialist articulates and executes the agreed regulatory strategy for assigned corporate projects. Leads the creation, development, and implementation of global/regional regulatory affairs procedures for marketed products and to maintain, update or remediate company’s regulatory compliance status. Essential Functions & Accountabilities: Registration Activity Reviews and approves regulatory documents for the registration of current and new products in assigned markets. Oversees the maintenance of submission documents, and agile databases in an accurate, complete and timely manner to ensure prompt and accurate access to company regulatory information. Maintains, updates and remediates regulatory files and documents as required. This includes maintaining communication across the EMEA RA team and other departments, sites, or business units, to provide regulatory status reports. Coaches/Mentors more junior team members with submission Monitoring Registration Requirements within Region Maintains up-to-date knowledge of regional and national regulations, guidelines, and advisory documents required for marketing CooperVision products in a specified region. Communicates applicable regulatory requirements to CooperVision Regulatory Affairs management and business partners. Analyses impact and communicate to management changes in regulations or requirements that have been identified. Establish and leverage working relationships with government, regulatory agencies, and trade associations for the purpose of advocating CooperVision positions Technical Documentation Reviews compiled Technical Files for CE approval prior to submission Supports RA Management with Notified Body requests for information. As required, plays a significant role in technical audits in the UK, EU, ACE and MENA region, i.e. preparation, contingency planning, response, findings and close out activities. Support to CooperVision Processes Represents the perspective of regulatory affairs to the company. Interprets general business objectives and effectively present information to manager and regions. Reviews and approves product labelling. Initiates IFUs and other required product labelling in line with relevant UK, EU, ACE & MENA requirements. Supports “Own Brand” and “Private label “customers and liaises with EU Competent Authorities and other Ministries of health as necessary Provides input to Regulatory Affairs Impact Documents (RAIDS) from UK EU, ACE & MENA perspective. Undertakes other administrative tasks to support CE marking and regional registrations. Responsible for exhibiting professional behaviour with internal and external business associates that reflect positively on CooperVision, The individual conveys a trustworthy, credible, and reliable image at all times. Act as a resource to the regions on quality issues and propose changes to minimise risks and enhance quality, reliability, safety and productivity. Act as spokesperson, when appropriate, regarding CooperVision practices, public policy, business interests; arrange for technical explanations from internal or external experts. Support RA compliance activities as necessary in assigned regions Independently manage multiple projects, department initiatives and day to day tasks About you: Experience: 6-8 years of medical device regulatory experience. Technical writing experience. Has experience evaluating manufacturing changes for impact on global regulatory affairs submissions. Medical device industry experiences including strong working knowledge and experience with MDD and MDR. Ability to operate in a business-driven model providing quick, salient analysis and concrete action plans emphasis on understanding and anticipating business needs and interests and devising proactive approaches/responses. Must have the ability to build relationships and influence decision makers. Comprehension of industry developments and changes in the political environment. Extensive network-building and contact experience. Capability to interact effectively and credibly at senior levels. Experience in electronic document management systems Strong IT skills, problem solving ability, analytical and communication skills. Knowledge, Skills and Abilities: Understanding of ISO 13485 requirements and EU medical device regulations. Ability to read and understand technical material. Excellent attention to detail Excellent organizational skills Excellent written and verbal communication skills. Excellent organizational skills. Computer literate, with intermediate skill in the use of Word, Excel and Outlook, and some knowledge of relational database systems, e.g. Agile Project Management system. Ability to work effectively either alone or as part of a team. Managing time effectively and completing tasks on time with general supervision. Experienced at reviewing and approving product labelling. Flexible and able to self-manage multiple priorities. Able to work effectively in multinational/multicultural environments. Flexibility to work across the UK sites Full, current driving license What we offer: You’ll receive competitive compensation and a fantastic benefits package. We are committed to our employees’ personal and professional development and offer extensive training to support your career growth and help every individual to reach their full potential. To help us achieve our goals, we’ll give you everything you need to help you achieve yours. We also provide access to LinkedIn Learning to help you develop in you career and grow with CooperVision. If you like what you see, take the first step towards your Brighter Future and apply today! All suitably qualified applicants will receive equal consideration and opportunities from CooperVision. # ONSITE #LI-JS1 |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | day |
| Source URL | https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/10823 |
| Apply URL | https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/10823 |
| First Seen At | 2026-05-31 17:56:25Z |
| Last Seen At | 2026-06-06 18:54:57Z |
| Last Checked At | 2026-06-06 18:54:57Z |
| Last Changed At | 2026-05-31 17:56:25Z |
| Inactive At | — |
| Source Posted At | 2026-04-14 13:29:37Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hcjy.fa.us2.oraclecloud.com|CX_1/date=2026-06-06/2026-06-06T18-54-41-336Z-a5965b54189b18264a41117402013b6b0f9a2ca665e465fc49b0f52e26911a85.json |
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"ExternalDescriptionStr": "<p style=\"margin-bottom:0cm;\"><strong>Job title:</strong> Principal Regulatory Affairs Specialist - EMEA</p><p style=\"margin-bottom:0cm;\"><strong>Department:</strong> Regulatory Affairs <span> </span></p><p style=\"margin-bottom:0cm;\"><strong>Location: </strong>Southampton, UK / Gorinchem, Netherlands or Gothenburg, Sweden <span> </span></p><p style=\"margin-bottom:0cm;\"><strong>GLS:</strong> P04</p><p style=\"margin-bottom:0cm;\"><strong>Working hours:</strong> UK – 37.5 hours per week, Netherlands or Sweden – 40 hours per week <span> </span></p><p> </p><p><span style=\"color:black;\"><strong>A brighter future awaits you</strong></span></p><p> </p><p><strong>What to expect: </strong></p><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"color:black;\"><span lang=\"EN-US\">The Principal Regulatory Affairs Specialist will provide expert level regulatory support and direction across our UK&I, BeNeLux and Nordic Clusters, for products from concept to launch, and beyond into post market, as well as regulatory processes. The Principal RA Specialist articulates and executes the agreed regulatory strategy for assigned corporate projects. Leads the creation, development, and implementation of global/regional regulatory affairs procedures for marketed products and to maintain, update or remediate company’s regulatory compliance status.</span></span></p><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"color:black;\"><span lang=\"EN-US\"><u>Essential Functions & Accountabilities:</u></span></span></p><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"color:black;\"><span lang=\"EN-US\">Registration Activity</span></span></p><ul style=\"list-style-type:disc;padding-left:72px;\"><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Reviews and approves regulatory documents for the registration of current and new products in assigned markets.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Oversees the maintenance of submission documents, and agile databases in an accurate, complete and timely manner to ensure prompt and accurate access to company regulatory information.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Maintains, updates and remediates regulatory files and documents as required. This includes maintaining communication across the EMEA RA team and other departments, sites, or business units, to provide regulatory status reports.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Coaches/Mentors more junior team members with submission </span></span></p></li></ul><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"color:black;\"><span lang=\"EN-US\">Monitoring Registration Requirements within Region</span></span></p><ul style=\"list-style-type:disc;padding-left:72px;\"><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Maintains up-to-date knowledge of regional and national regulations, guidelines, and advisory documents required for marketing CooperVision products in a specified region.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Communicates applicable regulatory requirements to CooperVision Regulatory Affairs management and business partners.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Analyses impact and communicate to management changes in regulations or requirements that have been identified.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Establish and leverage working relationships with government, regulatory agencies, and trade associations for the purpose of advocating CooperVision positions</span></span></p></li></ul><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"color:black;\"><span lang=\"EN-US\">Technical Documentation</span></span></p><ul style=\"list-style-type:disc;padding-left:72px;\"><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Reviews compiled Technical Files for CE approval prior to submission </span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Supports RA Management with Notified Body requests for information.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">As required, plays a significant role in technical audits in the UK, EU, ACE and MENA region, i.e. preparation, contingency planning, response, findings and close out activities.</span></span></p></li></ul><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"color:black;\"><span lang=\"EN-US\">Support to CooperVision Processes</span></span></p><ul style=\"list-style-type:disc;padding-left:72px;\"><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Represents the perspective of regulatory affairs to the company.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Interprets general business objectives and effectively present information to manager and regions.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Reviews and approves product labelling. Initiates IFUs and other required product labelling in line with relevant UK, EU, ACE & MENA requirements.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Supports “Own Brand” and “Private label “customers and liaises with EU Competent Authorities and other Ministries of health as necessary</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Provides input to Regulatory Affairs Impact Documents (RAIDS) from UK EU, ACE & MENA perspective.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Undertakes other administrative tasks to support CE marking and regional registrations.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Responsible for exhibiting professional behaviour with internal and external business associates that reflect positively on CooperVision, The individual conveys a trustworthy, credible, and reliable image at all times.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Act as a resource to the regions on quality issues and propose changes to minimise risks and enhance quality, reliability, safety and productivity.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Act as spokesperson, when appropriate, regarding CooperVision practices, public policy, business interests; arrange for technical explanations from internal or external experts.</span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Support RA compliance activities as necessary in assigned regions </span></span></p></li><li><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;margin-right:0cm;margin-top:0cm;\"><span style=\"color:black;\"><span lang=\"EN-US\">Independently manage multiple projects, department initiatives and day to day tasks</span></span></p></li></ul><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"> </p><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"background-color:white;color:black;\"><strong><u>About you:</u></strong></span></p><p><span lang=\"EN-US\">Experience:</span></p><ul style=\"list-style-type:disc;padding-left:33.4px;\"><li><span lang=\"EN-US\">6-8 years of medical device regulatory experience.</span></li><li><span lang=\"EN-US\">Technical writing experience. Has experience evaluating manufacturing changes for impact on global regulatory affairs submissions.</span></li><li><span lang=\"EN-US\">Medical device industry experiences including strong working knowledge and experience with MDD and MDR. </span></li><li><span lang=\"EN-US\">Ability to operate in a business-driven model providing quick, salient analysis and concrete action plans emphasis on understanding and anticipating business needs and interests and devising proactive approaches/responses.</span></li><li><span lang=\"EN-US\">Must have the ability to build relationships and influence decision makers.</span></li><li><span lang=\"EN-US\">Comprehension of industry developments and changes in the political environment.</span></li><li><span lang=\"EN-US\">Extensive network-building and contact experience.</span></li><li><span lang=\"EN-US\">Capability to interact effectively and credibly at senior levels.</span></li><li><span lang=\"EN-US\">Experience in electronic document management systems</span></li><li><span lang=\"EN-US\">Strong IT skills, problem solving ability, analytical and communication skills.</span></li></ul><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"> </p><p><span lang=\"EN-US\">Knowledge, Skills and Abilities:</span></p><ul style=\"list-style-type:disc;padding-left:33.4px;\"><li><span lang=\"EN-US\">Understanding of ISO 13485 requirements and EU medical device regulations.</span></li><li><span lang=\"EN-US\">Ability to read and understand technical material.</span></li><li><span lang=\"EN-US\">Excellent attention to detail</span></li><li><span lang=\"EN-US\">Excellent organizational skills</span></li><li><span lang=\"EN-US\">Excellent written and verbal communication skills.</span></li><li><span lang=\"EN-US\">Excellent organizational skills.</span></li><li><span lang=\"EN-US\">Computer literate, with intermediate skill in the use of Word, Excel and Outlook, and some knowledge of relational database systems, e.g. Agile Project Management system.</span></li><li><span lang=\"EN-US\">Ability to work effectively either alone or as part of a team. Managing time effectively and completing tasks on time with general supervision.</span></li><li><span lang=\"EN-US\">Experienced at reviewing and approving product labelling.</span></li><li><span lang=\"EN-US\">Flexible and able to self-manage multiple priorities.</span></li><li><span lang=\"EN-US\">Able to work effectively in multinational/multicultural environments.</span></li><li><span lang=\"EN-US\">Flexibility to work across the UK sites</span></li><li><span lang=\"EN-US\">Full, current driving license</span></li></ul><p> </p><p> </p><p> </p><p><strong>What we offer:</strong></p><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"background-color:white;color:black;\">You’ll receive competitive compensation and a fantastic benefits package.</span></p><p><span>We are committed to our employees’ personal and professional development and offer extensive training to support your career growth and help every individual to reach their full potential. To help us achieve our goals, we’ll give you everything you need to help you achieve yours. </span></p><p style=\"background-color:white;line-height:normal;margin-bottom:9.0pt;\"><span style=\"color:black;\">We also provide access to LinkedIn Learning to help you develop in you career and grow with CooperVision.</span></p><p> </p><p><span><strong>If you like what you see, take the first step towards your Brighter Future and apply today! All suitably qualified applicants will receive equal consideration and opportunities from CooperVision.</strong></span></p><p> </p><p>#<span style=\"color:black;\"><span class=\"normaltextrun\" style=\"border:none windowtext 1.0pt;padding:0cm;\">ONSITE</span></span></p><p>#LI-JS1</p>",
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