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United Kingdom (UK) 🛡️ UK Work Eligibility 💼 Company - Public
Mondelēz International - research scientist
Mondelēz International ✓ Verified Employer

research scientist

📍 Reading, England 🕒 2 days ago
Verified Base Compensation
£43,218 - £33,765 / year
£3,602 - £2,814 / mo Apply Now →
Official Specifications

Role Overview & Mandate

Executive Summary

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research scientist Reading, England

Job Description

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 and help us deliver real world solutions for a brighter future!

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.

The scope includes troubleshooting and optimisation of pharmacopeia methodology, verification of analytical methods for excipients, APIs and biologics and driving client drug delivery programs from the raw materials through to their finished products and stability studies.

The Senior Scientist II role 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 :

Technical

  • 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.

Communication & Influence

  • Work as part of an efficient analytical team

  • To liase with clients, business development and line management to ensure effective communication of project proposals and results.

  • Provide expert advice and lead client and stake holders meetings and audits

  • Deliver presentations to clients and stakeholders

  • Contribute to both technical and business strategy including influencing senior management

Leadership and supervision

  • Use Technical expertise to coach/ mentor a team of Scientists and Technicians

  • Plan own workload and projects for junior staff

  • Train and coach junior members of the team as required.

QEHS

  • Work to the highest standards of safety and quality by ensuring that appropriate COSHHs, risk assessments and SOPs are understood and followed.

  • To complete, review and approve assigned quality actions on a timely manner.

  • Write, approve and review SOPs and Test Methods

  • Generation and approval of Risk Assessments and COSHH

  • Understand and provide technical regulatory leadership in client audits

  • To ensure the maintenance of a clean, tidy and safe working environment for both yourself and members of the team

  • To understand and work to the requirements of GMP; including client specific quality requirements and pharmacopeia requirements.

  • Ensure training records are accurate for both yourself and members of the team.

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).

No Relocation support available

Business Unit Summary

Reading Scientific Services Ltd (RSSL) is a cutting-edge contract research organisation (CRO), providing research, analysis and consultancy to the food, consumer goods and life science sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 70 countries. Enriched by our parent company, Mondelēz International, our team are committed to transforming lives through science, innovation and collaboration.

Curious about us and want to learn more?

Please explore : Website YouTube LinkedIn Glassdoor

RSSL is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

#RSSL

Job Type

Regular

Analytical Science

Science & Engineering
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Compensation Analytics

Estimated Take-Home Pay

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Projected statutory deductions based on standard single-filer baseline tax regulations in the United Kingdom corridor.

Gross Annual Package £43,218 - £33,765
Est. Income Tax Band 20% Basic Rate Band
Statutory Insurance / FICA 8% Class 1 National Insurance (NI)
Estimated Monthly Net £2,251 - £2,809 / mo
Regional Economics

Cost of Living (Reading, England)

Bureau Data
Est. Rent (1-Bed)
£1,100 - £1,750
Monthly Utilities
£140 - £210
Cost Index
112.5
Disposable Tier
Top 15% Rank
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Compliance Standards

Work Authorization Framework

Verified Status: UK Work Eligibility
Corridor: UK Employment Corridor
🛡️ Zero Fee: Direct corporate recruitment with zero placement charges.

Candidate Selection Pipeline

Direct Corridor Track
01
Direct Apply

Submit verified credentials & CV.

02
HR Screening

2-4 day credential verification.

03
Technical Panel

In-depth domain & team interview.

04
Official Offer

Corridor contract & relocation.

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