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🟒 Actively Hiring Β· Posted 24d ago ⏳ Closes in 67 days UK Corridor πŸ›‘οΈ UK Work Eligibility 🏒 Company - Private

Scientist

Salary Range
Salary Disclosed on Application
Full Benefits Package

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This vacancy has been independently reviewed by the OppaJob Transatlantic Career Intelligence Desk to confirm authentic direct employer recruiting, verify compensation transparency, and eliminate applicant processing fees.

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Corporate Registration Verified UK Companies House registration standing active
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Prevailing Wage Benchmark UK National Minimum Wage & Equality Act 2010 aligned
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Zero-Intermediary Direct Pipeline Direct candidate ATS submission. 100% free with zero recruitment charges.
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Corridor Right-to-Work Match UK Work Eligibility

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Verified Analytics
Location Base
United Kingdom
Tier-1 UK Economic Zone
Est. Take-Home Pay
68% - 74% (After PAYE & NI)
Single tax filer baseline
Transatlantic Parity
1.0 GBP β‰ˆ $1.28 USD Living Standard
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Position Overview & Specifications

Medical Devices

Surrey

(Β£) Competitive

permanent

Job Ref: 7718

Description

A medical device company has an exciting opportunity for a Scientist | to join their team.

You will be responsible for the laboratory work, primarily in medical device development. You will also be providing scientific and technical support to the team and reporting on progress on projects, along with monitoring risks to make sure deadlines are met.

You will require a scientific or engineering degree, and experience with product development projects within an ISO, IVD, GMP, or GLP environment.

The Role

  • Hands-on laboratory bench work, primarily in the area of medical device development.
  • Provide scientific and technical support to programs and projects.
  • Responsible for on-time and on-budget delivery of work packages within a project, including timely reporting of progress on projects and on metrics to monitor and mitigate risk and to ensure production deadlines are met.
  • Responsible for quality and regulatory compliance of work undertaken.
  • Independently keep a current knowledge base in relevant areas of scientific and technical research.
  • Manage the day-to-day running of assigned development projects within the Quality Management System and work to operating procedures.

Undertake additional ad-hoc tasks as required.

Experience Required

  • Degree in either Life Sciences or Engineering.
  • Basic laboratory skills including but not limited to, pipetting and reagent preparation.
  • Experience working to strict quality standards such as Medical Device regulations and standards including, but not limited to, CFR, EEC, IVD, EC, ISO, GMP, GLP, and QSR.
  • A strong understanding of the importance of accurate record-keeping within a strictly controlled quality system is essential.
  • Manage and deliver product development projects to agreed performance specifications, on time, and within budget.
  • An eye for detail and commitment to high-quality data.
  • A flexible, can-do approach to the requirements of the job.
  • Organisational skills and the ability to rapidly prioritize tasks in response to unexpected opportunities or risks.
  • Excellent accuracy and attention to detail in practical and written work.
  • Strong team player with excellent analytical and interpersonal skills.
  • Good report writing skills, with the ability to communicate results to technical and non-technical staff.
  • Ability to work independently with minimal supervision.
  • Continuous learner with a keen appetite for cross-disciplinary work.
  • Entrepreneurial thinking and work ethic.


Competitive Salary – Private Medical Care Plans – Bonus – Additional Benefits

Job Ref: 7718

Candidate Selection & Onboarding Process

1

Application & Resume Screening

Submit your tailored CV/Resume directly to the talent acquisition portal.

2

Technical & Competency Interviews

Virtual interviews with the hiring manager and multidisciplinary team.

3

Formal Offer & Benefits Negotiation

Written agreement outlining compensation, equity, retirement vesting, and relocation allowances.

4

Onboarding & Corporate Integration

Equipment provisioning, team orientation, and commencement of duties.

United Kingdom Right to Work & Skilled Worker Visa Guide

Corridor Intelligence

Employment in the United Kingdom requires legal Right to Work verified under the Home Office Points-Based Immigration System:

πŸ‡¬πŸ‡§ Skilled Worker Visa (Tier 2)

Sponsoring employers must hold an active Home Office A-rated Sponsor License and assign a valid Certificate of Sponsorship (CoS). Role must meet the general minimum salary threshold (Β£38,700) or occupation going rate.

πŸ›οΈ Settlement (ILR) Pathway

Continuous employment under Skilled Worker status establishes eligibility for Indefinite Leave to Remain (ILR) after 5 continuous years, leading to British Citizenship.

βš–οΈ Official regulatory reference: UK Visas and Immigration (UKVI) & Home Office Sponsor Register.

Candidate Preparation Blueprint: General

Recruitment Insights

Based on transatlantic hiring benchmarks for Scientist roles across Cranleigh Recruitment's corporate sector, successful applicants typically excel across three core dimensions:

1. Domain Competency

Demonstrated portfolio evidence, architecture/system design case studies, or validated professional certifications directly applicable to General.

2. Behavioral & Leadership

STAR method competency responses highlighting cross-functional leadership, conflict resolution, and delivering measurable enterprise ROI under tight timelines.

3. Compensation Alignment

Total compensation expectation aligned within the benchmarked Salary Disclosed on Application bracket, including retirement vesting and health parity.

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Hiring Organization
Cranleigh Recruitment

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Eligibility: UK Work Eligibility
Schedule: Company - Private
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