Technical support associate Work, Jobs in Southampton, Ham (with Salaries)

Principal Regulatory Affairs Specialist - EMEA (Cluster Partner)
CooperVision —Southampton
- Full-time
- Microsoft Outlook
- Computer literacy
- Analysis skills
Clinical Territory Associate
Intuitive Surgical —Southampton
- Day shift
- Up to 50% travel
- Sales
- English
3d
Graduate Construction Project Manager - Southampton or Basingstoke
AECOM —Southampton
- Full-time
- Hybrid work
- Engineering
- Master's degree
- Project management
Laboratory Analyst
Ecolab Inc. —Andover
- Full-time
- Engineering
- Laboratory experience
- Microsoft Office
- Employee stock purchase plan
Complex Injury Large Loss Lawyer - Senior Associate
Keoghs —Southampton
- Full-time
- Hybrid work
- Communication skills
- Employee discount
Quick apply
12d
JUNIOR SALES ADVISOR
Verisure Services (UK) Limited —Southampton
- £3,800 a month
- Full-time
- Sales
Quick apply
LEGAL ASSISTANT – PRIVATE CLIENT TEAM (Administration)
Scott Bailey LLP —Lymington
- Up to £27,000 a year
- Full-time
- Microsoft Office
- Administrative experience
- Organisational skills
- Free parking
- Annual leave
Quick apply
4d
Quality Assurance Technician - Weekend Nights
Rich Products Corporation —Andover
- 12 hour shift
- Bakery
- Annual leave
Complex Injury Assistant Lawyer - Associate
Keoghs —Southampton
- Full-time
- Hybrid work
- Analysis skills
- IT
- Communication skills
- Employee discount
Quick apply
13d
JUNIOR SALES CONSULTANT
Verisure Services (UK) Limited —Southampton
- £3,800 a month
- Full-time
- Sales
- Driving
Quick apply
Knowledge Base Manager
University of Southampton —Southampton
- £36,636 - £44,746 a year
- Full-time
- Hybrid work
- Analysis skills
- Driving
- Communication skills
10d
Tax Regulatory Change Associate
JPMorganChase —Bournemouth
- Full-time
- Accounting
- Financial services
- Communication skills
Associate Lecturer in English - Sessional
City of Portsmouth College —Portsmouth
- £30,248.30 - £44,298.68 a year
- Part-time
- English
- Education
- Construction experience
- Free parking
- Annual leave
Quick apply
11d
Associate Lecturer in Electrical Installation
City of Portsmouth College —Portsmouth
- £30,248.30 - £44,298.68 a year
- Part-time
- Computer literacy
- Teaching
- Free parking
- Annual leave
Quick apply
10d
Associate Project Manager
AECOM —Southampton
- Full-time
- Hybrid work
- Organisational skills
- Contracts
- Communication skills
Associate Lecturer in Maths - Sessional
City of Portsmouth College —Portsmouth
- £30,248.30 - £44,298.68 a year
- Part-time
- Maths
- Education
- Communication skills
- Free parking
- Annual leave
Quick apply
11d
Associate Surveyor - Valuation
Vail Williams —Southampton
- Full-time
- Hybrid work
- Analysis skills
- Leadership
- Communication skills
- Flexible schedule
Quick apply
Senior/Principal/Associate Civil/Structural Engineer
Ramboll —Southampton
- Full-time
- Civil engineering
- Engineering
- Master's degree
Quick apply
Core Real Estate Associate, Southampton
Bryan Cave Leighton Paisner LLP —Southampton
- Sales
- Analysis skills
Quality Assurance Technician - Weekend Days
Rich Products Corporation —Andover
- Weekend availability
- Bakery
- Annual leave

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technical support associate jobs near southampton, ham

Principal Regulatory Affairs Specialist - EMEA (Cluster Partner)

CooperVision -
Southampton

Apply Now

Job details

Full-time

Qualifications

Driving Licence
Microsoft Outlook
Relational databases
Computer literacy
Analysis skills
Organisational skills
Technical writing
Agile
IT
Document management systems
Communication skills

Full job 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

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

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.

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Refine Your Search

technical support associate jobs in southampton, ham

Principal Regulatory Affairs Specialist - EMEA (Cluster Partner)

Clinical Territory Associate

Graduate Construction Project Manager - Southampton or Basingstoke

Laboratory Analyst

Complex Injury Large Loss Lawyer - Senior Associate

JUNIOR SALES ADVISOR

LEGAL ASSISTANT – PRIVATE CLIENT TEAM (Administration)

Quality Assurance Technician - Weekend Nights

Complex Injury Assistant Lawyer - Associate

JUNIOR SALES CONSULTANT

Knowledge Base Manager

Tax Regulatory Change Associate

Associate Lecturer in English - Sessional

Associate Lecturer in Electrical Installation

Associate Project Manager

Associate Lecturer in Maths - Sessional

Associate Surveyor - Valuation

Senior/Principal/Associate Civil/Structural Engineer

Core Real Estate Associate, Southampton

Quality Assurance Technician - Weekend Days

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