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🟢 Actively Hiring · Posted 24d ago ⏳ Closes in 67 days UK Corridor 🛡️ UK Work Eligibility 🏢 Company - Private

research scientist

Salary Range
£40,000 / yr
£3,333 / mo

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OP-VERIF-61EB0B60 ✓ Passed Inspection

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

Transatlantic Cost of Living & Purchasing Power Benchmark

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

Are you looking for a rewarding role where you can make a positive impact, working with the world's most innovative food and Life Sciences companies? Join our diverse team today!

Reading Scientific Services Ltd (RSSL) is a cutting-edge Contract Research Organisation (CRO), providing research, analysis and consultancy to the life science, healthcare and food sectors.

As a senior scientist, the role of Chromatography Expert is to provide analytical expertise across the breadth of Pharmacopoeia and client methodology required during the drug life cycle. You will play a key role in ensuring that chromatography projects within the Pharmaceutical Development laboratory are performed and supervised effectively and accurately within agreed timescales and to appropriate quality standards. The role will coach a team of scientists, providing technical direction, and will be responsible for reviewing and authorising of certificates of analysis, interpretive scientific reports, verifications and validations and authorizing competencies within the area of expertise.

Primary Accountabilities / Responsibilities :

  • Provide high quality customer service at all times by ensuring effective organisation of assigned workload, integrity of analytical data generated and timely/accurate provision of results.
  • Responsible for a portfolio of analytical projects including verification, validation and transfer of pharmaceutical chromatographic methodology.
  • Implementation of solutions to technical pharmacopoeia challenges and support creation of new business opportunities
  • Perform data checking and provide interpretation of results for routine and complex testing
  • Generate certificate analysis and external interpretive reports.
  • Expert user in the use of software packages relevant to the role, Laboratory’s LIMS system, Q-Pulse, Chemwatch, Openlab.
  • Provide training and supervise staff in routine activities, methods and interpretation.
  • Provide technical direction in area of expertise within and across departments, including maintenance and troubleshooting of laboratory equipment.
  • To understand and work to the requirements of GMP; including client specific quality requirements and pharmacopeia requirements.

Knowledge, Skills, Experience and Language Requirements :

  • Educated to Degree or PhD in a relevant scientific discipline or over 8 years of industry experience
  • Excellent understanding of pharmaceutical lab equipment, HPLC, Dissolution, Karl Fischer, Stability Cabinets, etc.
  • In-depth knowledge of both technical area of expertise & business environment including regulatory requirements
  • Good knowledge of laboratory quality and accreditation systems (GMP)
  • Strong written and spoken communication skills, with the ability to influence, network and manage internal/external relationships.
  • Excellent organisational skills including time management and priority setting. Able to lead resource allocation in order to deliver projects to tight timescales.
  • Meticulous attention to detail, well organized and strong team working ethos.
  • Experienced in managing and mentoring staff
  • Technical credibility to develop good working relationships with internal and external clients.
  • Ability to solve complex analytical problems
  • Computer literate in standard MS office applications
  • The individual in this position has extensive experience in their discipline (both technical and regulatory) and has a demonstrated track record of applying their knowledge across different business areas.
  • Proven experience in Analytical Project Management
  • Experience in pharmaceutical laboratory quality systems (GMP)
  • English fluency (written and spoken)

In return for your commitment, drive and enthusiasm, we offer an attractive benefits package within a highly successful international business that offers financial rewards and resources, including:

  • Opportunities to learn and develop
  • Flexible working
  • Performance Related Bonus scheme
  • Contributory pension (up to 11% employer contribution)
  • Life assurance
  • Private medical insurance cover (can add partner and/or family) if applicable
  • 27 days holiday allowance (possibility to buy 5 extra days) + bank holidays
  • Employee Assistance Programme (EAP)
  • A flexible benefits programme (Gym discounts, private health insurance, restaurant discounts, etc).

Job Types: Full-time, Permanent

Salary: From £40,000.00 per year

Benefits:

  • Company pension

Supplemental pay types:

  • Bonus scheme

Application question(s):

  • What is your salary expectation?

Work authorisation:

  • United Kingdom (preferred)

Work Location: In person

Reference ID: Chromo 010

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:

🇬🇧 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 (£38,700) or occupation going rate.

🏛️ 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.

⚖️ Official regulatory reference: UK Visas and Immigration (UKVI) & Home Office Sponsor Register.

Candidate Preparation Blueprint: Biotech & Pharmaceuticals

Recruitment Insights

Based on transatlantic hiring benchmarks for research scientist roles across Reading Scientific Services'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 Biotech & Pharmaceuticals.

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 £40,000 / yr bracket, including retirement vesting and health parity.

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Hiring Organization
Reading Scientific Services

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Location: Reading, England
Eligibility: UK Work Eligibility
Schedule: Company - Private
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