Food Scientist Job at Cargill (London)

Senior Food and Drink Scientist

Supporting food manufacturers and retailers with product innovation including: r...

Location

United Kingdom , Chipping Campden

Salary:

42000.00 - 55000.00 GBP / Year

Campden BRI

Expiration Date

Until further notice

Requirements

Extensive experience in an R&D, or similar, role for a food or ingredients manufacturer
A degree in food science/ technology or similar.
A PhD in food science/chemical engineering/similar with a focus on development of analytical methods, experimental design, execution, statistical analysis, scientific writing, project management, and presenting at conferences.
Significant knowledge of food science and technology and analysis of physical properties such as rheology, texture, structure and thermal properties is essential
Extensive knowledge of, and experience with, functionality of emulsifiers, proteins, starches and hydrocolloids
Experience in using instrumental techniques to investigate raw materials or product properties.
Experience in data analysis from the above and familiarity with statistical analysis techniques required.
Project management skills.

Job Responsibility

Manage and undertake work on behalf of clients
Write reports for contract and research projects
Provide advice to clients
Identify new business opportunities
Contribute to idea generation for food and beverage science and research
Generate proposals for client work
Participate in conducting training both scheduled and tailor made

What we offer

Reward platform with employee discounts and rewards
25 days holiday + 8 bank holidays
Buy and sell holiday scheme
A generous work save pension scheme, with employee contributions matched by the company up to 10%
Culture focus around work/life balance (early finish Fridays)
Subsidised onsite restaurant

Fulltime

Group Leader – Microbiome Modelling and Host–Microbe Interactions

We’re looking for an ambitious and collaborative Group Leader or Career Track Gr...

Location

United Kingdom , Norwich

Salary:

Not provided

Quadram Institute

Expiration Date

February 15, 2026

Requirements

Excellent publication record
Evidence of establishing and supporting a productive research group
Supported by national research council grants (e.g., UKRI or equivalent) at a level commensurate for career stage
Clear vision for collaborative research
Diverse disciplinary backgrounds including microbiology, biochemistry, bioinformatics, computational biology, nutrition science, immunology, gastroenterology, analytical chemistry, and bioengineering
Vision for advancing microbiome science through innovative methodological approaches
Enthusiasm for collaborative, translational research

Job Responsibility

Build an independent research program focused on developing innovative microbiome models, assays, or analytical approaches
Advance mechanistic understanding of diet-microbiome-host interactions
Bridge technological innovation with biological insight
Align research with strategic priorities in nutrition science, sustainable food systems, and translational health research
Deliver on Institute core research objectives
Develop a broad research grant portfolio including collaborative projects with other scientists and stakeholders in industry and government

What we offer

Significant support package with an equivalent value up to £500,000 including a Postdoctoral Research Assistant, start-up package, budget for consumables and other research expenses
Access to core services including next generation sequencing and bioinformatics, advanced bioimaging, and Human Studies
Exciting, innovative and supportive research environment
Competitive salaries (depending on qualifications and experience)
Relocation package available
Range of family, faith and diversity friendly working arrangements

Fulltime

!

R&D Co-Op

Rich's, also known as Rich Products Corporation, is a renowned family-owned food...

Location

United States , Buffalo

Salary:

24.00 - 32.00 USD / Hour

OysterLink

Expiration Date

Until further notice

Requirements

Currently enrolled in a bachelor's or master’s degree program in food science or food engineering
available for a 12-month co-op starting spring 2026
ability to work in a laboratory and pilot wet lab environment
ability to lift and carry up to 50 lbs
ability to stand for extended time
ability to safely handle chemicals and cleaning agents with provided personal protective equipment
excellent communication skills
ability to follow safety protocols
willing to work in varying temperature environments
experience with baked goods, dairy and emulsion type food products preferred

Job Responsibility

Develop, document and validate product and process interactions in collaboration with global scientists and engineers
work in the pilot lab and operate equipment to make various product samples
conduct routine analytical and performance evaluations accurately and efficiently
maintain a lab notebook by recording results and completing data analysis
organize and prioritize tasks related to project work
summarize results in technical reports and assist in the interpretation of data from experiments and analysis

What we offer

competitive compensation
Health Insurance
financial benefits
Paid Time Off
Parental leave
family planning support
flexible work policy

Fulltime

Quality Control Analyst

Quality Control Analyst (East Windsor, NJ) (Multiple Openings)

Location

United States , East Windsor

Salary:

Not provided

Novitium Pharma

Expiration Date

Until further notice

Requirements

Must have bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related besides 1 year exp. as Quality Control Analyst / Chemist / Analyst / Scientist / Research Associate / Microbiologist / Related

Job Responsibility

Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies
conduct testing and analysis of pharmaceutical raw materials like drug substance, excipients and packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry
Conduct testing and analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions. The dosage forms include food supplements like vitamin capsules, mineral tablets, and multivitamin syrups

Packaging Technician

We offer commercial analytical lab chemistry testing for food and drink, includi...

Location

United Kingdom , Chipping Campden

Salary:

Not provided

Campden BRI

Expiration Date

Until further notice

Requirements

A-levels (or equivalent) in Science, Food Technology, or a related subject or relevant practical/lab experience
Basic IT skills (e.g. Microsoft Word, Excel, Outlook)
Good communication skills and a willingness to work as part of a team
The ability to organise your own work and follow procedures carefully
Hold a full UK driving license and have own vehicle
Right to work in the UK by the start of employment

Job Responsibility

Preparing samples and carrying out packaging tests following written methods
Supporting contract testing projects and research work
Maintaining laboratory and pilot plant equipment
Keeping accurate records and logs of work carried out
Supporting good housekeeping, hygiene and safety in the lab
Working closely with scientists and technicians in a small, friendly team

What we offer

Reward platform with employee discounts and rewards
25 days holiday + 8 bank holidays
Buy and sell holiday scheme
A generous work save pension scheme, with employee contributions matched by the company up to 10%
Culture focus around work/life balance (early finish Fridays)
Subsidised onsite restaurant

Fulltime

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Process Development Senior Scientist - Attribute Sciences

Join Amgen’s Mission of Serving Patients. This is an exciting opportunity to joi...

Location

United States , Cambridge

Salary:

136692.00 - 164965.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 5 years of Scientific experience
Master’s degree and 3 years of Scientific experience
Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable]
Strong written and verbal communication skills, ability to support data-driven decision making with diverse internal and external stakeholders
5+ years of experience in industrial analytical laboratories supporting characterization of protein therapeutics, including partnering with QC and/or CMOs on method execution
Deep LC/MS expertise in bottom‑up peptide mapping (including disulfide mapping) and intact mass analysis for biologics, with strong fundamentals in sample preparation, artifact control, and MS/MS data interpretation
Hands-on experience with Thermo Orbitrap platforms (e.g., Q-Exactive, Exploris, Tribrids), including routine maintenance, calibration, and independent troubleshooting of common failure modes (sensitivity loss, spray instability, mass accuracy drift, carryover/contamination)
Strong RP‑UHPLC expertise (reversed‑phase method development and troubleshooting) to support peptide mapping/intact workflows (gradient optimization, column selection, carryover mitigation, pressure/peak‑shape troubleshooting)
Hands-on experience with laboratory automation including liquid handlers, pipetting robots, and automation software
Familiarity with United States Pharmacopeia (USP), International Conference on Harmonization (ICH), and Food & Drug Administration (FDA) guidance documents related to analytical method transfer and validation

Job Responsibility

Lead late-stage protein structural elucidation and forced degradation studies using LC/MS workflows including reduced peptide mapping, disulfide mapping, and intact mass analysis
effectively communicate results to support regulatory filings
Maintain, troubleshoot, and optimize high-resolution mass spectrometry methods
partner with instrument vendors and application specialists as needed to ensure reliable performance, consistent data quality, and high instrument uptime
Develop, optimize, and qualify LC/MS and complementary LC-UV protein characterization methods to identify and monitor critical quality attributes
coordinate with program leads to identify and implement control strategies
Lead training, qualification, and method transfer from our process development labs to our global quality network
Interpret analytical results, author and review technical protocols/reports, and contribute to analytical CMC sections in regulatory filing documents including IND and BLAs
Design automation-ready MS workflows including sample preparation, instrument integration, data processing, and report generation to reduce hands-on time and increase lab efficiency
Build robust, inspection-ready LC/MS data analysis and reporting workflows (templates, QC checks, method trending) and ensure traceability and data integrity for CMC deliverables

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans

Fulltime

New

Technical Product Owner

Technical Product Owner - up to £55,000 Per Annum DOE. Are you ready to transfor...

Location

United Kingdom , Newcastle

Salary:

55000.00 GBP / Year

Parking Network B.V.

Expiration Date

February 24, 2026

Requirements

3+ years in technical product ownership, ideally in consumer facing solutions
Proven ability to prioritise tasks based on business value, customer impact and technical feasibility
Strong technical knowledge to work with development teams and understand the architecture of transactional systems (API, databases, integrations)
Experience with technical documentation, system design and workflows to ensure clear communication with both technical and non-technical stakeholders
Ability to identify blockers and obstacles, work to resolve them and ensure project delivery on time
Experience with Agile Frameworks and tools

Job Responsibility

Manage and prioritise the product backlog, creating actionable user stories and acceptance criteria to guide the development team
Over see the execution of key features like mobile app updates, booking engines and parking space sensors to meet user and business needs
Act as a liaison between business stakeholders and our technical team, ensuring clear communication and alignment on goals
Work closely with Developers to ensure technical feasibility, system performance and compliance with security and industry standards
Address and resolve technical issues in a timely manner, minimising disruptions to system functionality
Analyse data to recommend improvements

What we offer

Annual leave: A fantastic 25 days annual leave + 8 Bank Holidays
Pension: Comprehensive pension plan to secure your future
Private Healthcare: Private healthcare for peace of mind
Discretionary bonus: Recognition for your contribution

Fulltime

Food Scientist

Cargill

Location:
Canada , London

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 23, 2025

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