124 Scientific Internship jobs in the United Kingdom

Our client, a pioneering biotechnology company based in **Newcastle upon Tyne, Tyne and Wear, UK**, is seeking an experienced Senior Scientific Research Associate to contribute to their groundbreaking work in drug discovery and development. This role is crucial for advancing our client's pipeline by conducting rigorous scientific research, developing innovative assays, and troubleshooting complex experimental challenges. The ideal candidate will possess a strong background in molecular biology, biochemistry, or a related field, with hands-on experience in a research and development laboratory setting. You will be responsible for designing, executing, and analyzing experiments, meticulously documenting findings, and contributing to the interpretation of data within a broader research program. The Senior Scientific Research Associate will play a key role in optimizing existing protocols and developing novel methodologies to accelerate research timelines. This position demands excellent problem-solving skills, a keen eye for detail, and the ability to work independently while also collaborating effectively with a multidisciplinary team of scientists. Maintaining a safe and organized laboratory environment, adhering to GLP/GMP standards, and staying current with scientific literature are also integral aspects of this role. This is an exceptional opportunity to join a dynamic team at the forefront of scientific innovation and make a tangible contribution to developing life-changing therapeutics.

Responsibilities:

• Design, perform, and optimize complex experiments in molecular biology and biochemistry.
• Develop and validate new assays and experimental protocols.
• Analyze experimental data using appropriate statistical methods and software.
• Troubleshoot experimental issues and identify solutions.
• Accurately record and meticulously document all experimental procedures and results in electronic lab notebooks.
• Collaborate with project teams, present findings, and contribute to research strategy discussions.
• Maintain laboratory equipment and ensure compliance with safety regulations.
• Stay updated on relevant scientific literature and emerging technologies.
• Contribute to manuscript preparation and patent applications as needed.

Qualifications:

• MSc or PhD in Molecular Biology, Biochemistry, Biotechnology, or a related life science discipline.
• Minimum of 5 years of post-graduate research experience in an industrial or academic R&D setting.
• Proven expertise in cell-based assays, molecular cloning, protein expression and purification, or similar relevant techniques.
• Strong understanding of drug discovery and development processes.
• Proficiency in data analysis software (e.g., GraphPad Prism, R).
• Excellent laboratory technique, attention to detail, and record-keeping skills.
• Strong written and verbal communication abilities.
• Ability to work independently and as part of a collaborative team.
• Experience with high-throughput screening (HTS) is a plus.

Join our client's dedicated team and contribute to significant advancements in biotechnology.

We currently have an exciting opportunity for a Scientific Officer to join our team in our laboratory, with a starting salary of £26,000 per annum.  This is a full time role working 8am - 4pm Monday - Friday.

At Future Health Biobank we are passionate about protecting the future health of children. Our focus is in two main areas: stem cell banking and genomics.

We are the largest stem cell bank in the UK and have been established for over 20 years. 

We now have a vacancy for a Scientific Officer to join our team.

Scientific officers are responsible for performing clean room equipment calibration according to the defined schedule, confirming that equipment is operating as per specified requirements before use, which ensures the accuracy of data being generated. Scientific officers perform procedures including the aseptic processing of samples within clean room environments involving cord blood volume reduction processing, cell culture, sterility testing and flow cytometry in accordance with standard operating procedures, guaranteeing that our client’s samples are processed and stored to the highest standards.

Key Responsibilities:

Sample Processing

• Aseptic processing of cord blood samples within the clean room
• Aseptic processing of cord tissue samples within the clean room
• Aseptic processing of tooth samples within the clean room
• Donor blood serology and PCR testing
• Ensuring environmental monitoring plates are incubated as per defined procedures and recording results
• Performing flow cytometry analysis on cord blood, cord tissue and dental pulp samples
• Perform cord tissue sterility testing
• Perform cord tissue post-thaw quality control testing
• Perform dental pulp post-thaw quality control testing

Daily equipment monitoring and laboratory set-up

• Set-up of clean room equipment and environment prior to use
• Report any equipment faults immediately to the Laboratory Manager
• Replenish clean room consumables and report any low stock levels to Laboratory Manager

External Qualification Programs (EQA)

• Testing of flow cytometry samples, microbiology, serology, PCR, blood analysis and ABO for the EQA program

Periodic facility/equipment maintenance and calibration

•  Environmental monitoring of clean room areas

Quality Management System

• To recognise the regulatory requirements for procurement, processing, testing, storage and disposal of human samples by reading, understanding and acknowledging the company policies and high-level documents assigned on Qpulse
• To recognise the procedure requirements for processing, testing, storage and disposal of human samples by reading, understanding and acknowledging the standard operating procedures (SOPs) assigned on Qpulse
• Ensuring the accuracy and validity of sample data generated through completion of equipment calibration and adherence to SOPs
• Ensuring the traceability of all samples through confirmation of sample codes and adherence to SOPs
• Raising of deviations for investigation by the Laboratory Manager
• Updating SOPs as per the change control procedure to ensure completeness and accuracy.

Qualifications & Experience:

• Bachelor’s degree in a scientific subject or a minimum of two years equivalent experience
• Good written and verbal communication skills
• Good computer literacy
• Attention to detail
• Ability to work as part of a team and independently
• Ability to follow and adhere to written standard operating procedures

Terms & Benefits:

• 37.5 hours per week,
• Salary of £26,000 per annum,
• 25 days holiday 

We currently have an exciting opportunity for a Scientific Officer to join our team in our laboratory, with a starting salary of £26,000 per annum.  This is a full time role working 8am - 4pm Monday - Friday.

At Future Health Biobank we are passionate about protecting the future health of children. Our focus is in two main areas: stem cell banking and genomics.

We are the largest stem cell bank in the UK and have been established for over 20 years. 

We now have a vacancy for a Scientific Officer to join our team.

Scientific officers are responsible for performing clean room equipment calibration according to the defined schedule, confirming that equipment is operating as per specified requirements before use, which ensures the accuracy of data being generated. Scientific officers perform procedures including the aseptic processing of samples within clean room environments involving cord blood volume reduction processing, cell culture, sterility testing and flow cytometry in accordance with standard operating procedures, guaranteeing that our client’s samples are processed and stored to the highest standards.

Key Responsibilities:

Sample Processing

• Aseptic processing of cord blood samples within the clean room
• Aseptic processing of cord tissue samples within the clean room
• Aseptic processing of tooth samples within the clean room
• Donor blood serology and PCR testing
• Ensuring environmental monitoring plates are incubated as per defined procedures and recording results
• Performing flow cytometry analysis on cord blood, cord tissue and dental pulp samples
• Perform cord tissue sterility testing
• Perform cord tissue post-thaw quality control testing
• Perform dental pulp post-thaw quality control testing

Daily equipment monitoring and laboratory set-up

• Set-up of clean room equipment and environment prior to use
• Report any equipment faults immediately to the Laboratory Manager
• Replenish clean room consumables and report any low stock levels to Laboratory Manager

External Qualification Programs (EQA)

• Testing of flow cytometry samples, microbiology, serology, PCR, blood analysis and ABO for the EQA program

Periodic facility/equipment maintenance and calibration

•  Environmental monitoring of clean room areas

Quality Management System

• To recognise the regulatory requirements for procurement, processing, testing, storage and disposal of human samples by reading, understanding and acknowledging the company policies and high-level documents assigned on Qpulse
• To recognise the procedure requirements for processing, testing, storage and disposal of human samples by reading, understanding and acknowledging the standard operating procedures (SOPs) assigned on Qpulse
• Ensuring the accuracy and validity of sample data generated through completion of equipment calibration and adherence to SOPs
• Ensuring the traceability of all samples through confirmation of sample codes and adherence to SOPs
• Raising of deviations for investigation by the Laboratory Manager
• Updating SOPs as per the change control procedure to ensure completeness and accuracy.

Qualifications & Experience:

• Bachelor’s degree in a scientific subject or a minimum of two years equivalent experience
• Good written and verbal communication skills
• Good computer literacy
• Attention to detail
• Ability to work as part of a team and independently
• Ability to follow and adhere to written standard operating procedures

Terms & Benefits:

• 37.5 hours per week,
• Salary of £26,000 per annum,
• 25 days holiday 

**Job Description**
**Are You Ready to Make an Impact at RSSL?**
**Join Our Mission to Transform Lives Through Science, Innovation and Collaboration**
At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research, consultancy, and training. We provide services to the food, pharmaceutical, and consumer goods industries, as well as our parent company, Mondelez International.
We are not just dedicated to delivering world-class scientific solutions and outstanding customer service, we are recognised for it. We were named Best Performing Professional Services Company of the Year (2025) at the One Nucleus Awards and CRO of the Year at the 2023 OBN awards. We were also finalists for multiple recent awards recognising our commitment to skills and rising talent.
**Purpose:**
In RSSL we are customer focused, science led and results driven. The RSSL Stability laboratory performs a wide range of ICH storage and stability studies for a variety of pharmaceutical and healthcare companies and supports Mondelez research and innovation.
In this role you will take responsibility for the administration of the stability programme, you will also contribute by performing a range of administrative and housekeeping tasks and performing a range of simple routine activities to support effective completion of projects and meet the customer's contractual agreements.
**Primary Accountabilities / Responsibilities:**
**Technical**
+ Provide high quality customer service at all times by ensuring effective organisation of assigned workload, integrity of data generated and timely/accurate provision of results.
+ To administer stability trials in a GMP-compliant manner by carrying out the initial stability trial setup and scheduling subsequent pulls on time and overseeing the daily maintenance of the stability cabinets.
+ To assist in the sub aliquoting samples for both internal and external customers and with sample receipt into the laboratory as required.
+ Assist with rountine checks/calibrations as required .Be competent in the use of generic and specific software packages required for the role including LIMS system and Q-PulsePerform Lab admin and housekeeping duties as directedWill be expected to work in different laboratories if the demand is required
**Communication & Influence**
+ Liaise with both internal and external clients as required to represent RSSL in a professional manner at all times.
**QEHS**
+ Work to the highest standards of safety and quality by ensuring that appropriate COSHHs, risk assessments and SOPs are understood and followed.
+ Assist in the control of all client documentation as required, ensuring that only the most current versions are supplied to analysts.
+ Prepare storage only protocols and external CoAs for review
+ To complete assigned quality actions on a timely manner
+ To maintain a clean, tidy and safe working environment.
+ To understand and work to the requirements of GMP.
+ Ensure training records are accurate.
**Knowledge, Skills, Experience and Language Requirements:**
+ Educated to A / HNC level in a relevant scientific discipline
+ Accountable, honest, hardworking and able to work efficiently in a team
+ Flexible and adaptable to meet customer/business requirements.
+ Meticulous attention to detail and an ability to follow written instructions.
+ Good written and verbal communication skills.
+ Self motivated, enthusiastic and quick to learn.
+ Well organized and capable of working on multiple activities concurrently.
+ Computer literate in standard MS office applications
+ Scientific understanding of stability chambers and the laboratory whilst working in a regulated environment
+ English fluency (written and spoken)
**More about this role**
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
+ Performance Related Bonus scheme
+ Contributory pension (between 8% to 11% employer contribution)
+ Life assurance
+ 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
Scientific Administration
Science & Engineering
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about.
We have a rich portfolio of strong brands - both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum
Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast.
Join us and Make It An Opportunity!
Mondelez Global LLC is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants who require accommodation to participate in the job application process may contact for assistance.

An exciting opportunity to join a small, collaborative pharmaceutical company as a Medical Affairs Scientist or Scientific Advisor. This role sits within a close-knit team of three and is responsible for providing internal and external scientific support — including medical education and scientific communications — to ensure that customer and patient needs are met. The Company This is a small but dynamic organisation offering a wonderfully broad remit and the chance to be involved in a wide range of medical affairs activities. Because of the company’s size, you will gain excellent visibility, have the chance to make a real impact, and develop a diverse skill set across multiple areas of medical affairs. The team is proactive, supportive, and fast-paced, working closely together to achieve results. The company operates a hybrid model, with office-based working in Hemel Hempstead three days per week. Salary range: £35,000 – £42,000 (depending on experience) plus package – a discussion is encouraged. Key Responsibilities Identify and engage HCPs using company resources such as social media, third-party data, and Veeva. Design and deliver medical education and training programmes. Develop scientific and medical materials for use at medical conferences and meetings. Maintain up-to-date product and competitor knowledge, acting as a regional expert. Actively contribute to brand team planning and the development of materials. Lead the development of medical resources and activities, ensuring they are fair, balanced, and compliant. Ensure all generated materials meet governance and compliance requirements, including maintaining training records and delivering compliance training/updates. Build and nurture strong cross-functional relationships (MSLs, Medical Information, Regulatory Affairs, Regional & Global teams, Brand, and Commercial). Required Qualifications & Experience BSc (or higher) with experience in the pharmaceutical industry or a related agency (medical communications/medical education). Strong project management skills with the ability to simplify complex medical messages. Proactive, solutions-oriented, and an excellent communicator with a collaborative mindset. Solid understanding of ABPI/PMCPA Code of Practice and medical governance. This role offers a fantastic opportunity to grow your career within a highly visible position, work closely with senior stakeholders, and gain hands-on experience across the breadth of medical affairs. For more information, please contact Julia Day at or

Role: (Senior) Scientific Director Location: UK (Hybrid – Manchester/Macclesfield/London) About Us Established in 2005, Bioscript Group has developed an outstanding reputation as a high-quality strategic partner to its pharmaceutical clients, providing support with regulatory submissions, market access strategy, clinical publications, medical education and commercialisation. We work collaboratively across functions and capabilities, sharing ideas and outputs to inform each other’s work and to learn from each other’s experience; providing many opportunities for personal and professional development. The Opportunity We are currently looking for a Scientific Director to be at the forefront of leading and implementing our scientific and strategic vision within our medical communications division. You will be required to provide strategic leadership (technical and scientific) of editorial teams with shared responsibility for driving the success and growth of key accounts. As a senior member of the team, our Scientific Director will also provide internal leadership and strategic planning for account growth. Key Responsibilities Collaborating proactively with cross-functional teams to evaluate and leverage scientific advances that drive new business opportunities Overall accountability and leadership across key accounts to deliver exceptional scientific quality through clear, concise, compliant and accessible content Ensuring adherence to industry guidelines and regulatory standards Working closely with the med comms leadership team to implement company objectives Management of designated line reports as required About You Established Scientific Director looking for a new challenge with increased responsibilities and senior leadership Flair for business development and an appetite for driving growth Confident presentation skills and evident leadership skills with a passion for communicating complex ideas backed up with strong customer focus Meticulous attention to detail and the ability to distil complex information for diverse audiences A proactive approach to learning and staying informed about industry trends Enthusiasm for working in a collaborative and dynamic environment Please note, this role may require domestic and international travel. Our people are at the heart of our business We are focused not just on delivering the exceptional for our clients, but for our teams too. We understand that everyone is different, and we believe in treating everyone as an individual with opportunities to develop your skills and career around our disciplines. Our benefits include: Salary which aligns with your experience and skillset 25 days holiday bank holidays winter shutdown holiday purchase scheme Enhanced sick and compassionate leave Enhanced maternity, paternity & adoption leave Birthday charity donation to a charity of your choice Bonus Day off to be spent giving back to the community Life Insurance and Critical Illness cover Private Medical (Vitality for UK-based colleagues) Health cash plan or wellbeing allowance International Employee Assistance Program We are committed to creating an inclusive and diverse workplace. We encourage applications from all individuals who meet the minimum requirements of the role. If you require any reasonable adjustments during the application or interview process, please contact us via or by calling .

An exciting opportunity to join a small, collaborative pharmaceutical company as a Medical Affairs Scientist or Scientific Advisor. This role sits within a close-knit team of three and is responsible for providing internal and external scientific support — including medical education and scientific communications — to ensure that customer and patient needs are met.

The Company

This is a small but dynamic organisation offering a wonderfully broad remit and the chance to be involved in a wide range of medical affairs activities. Because of the company’s size, you will gain excellent visibility, have the chance to make a real impact, and develop a diverse skill set across multiple areas of medical affairs. The team is proactive, supportive, and fast-paced, working closely together to achieve results. The company operates a hybrid model, with office-based working in Hemel Hempstead three days per week.

Salary range: £35,000 – £42,000 (depending on experience) plus package – a discussion is encouraged.

Key Responsibilities

• Identify and engage HCPs using company resources such as social media, third-party data, and Veeva.
• Design and deliver medical education and training programmes.
• Develop scientific and medical materials for use at medical conferences and meetings.
• Maintain up-to-date product and competitor knowledge, acting as a regional expert.
• Actively contribute to brand team planning and the development of materials.
• Lead the development of medical resources and activities, ensuring they are fair, balanced, and compliant.
• Ensure all generated materials meet governance and compliance requirements, including maintaining training records and delivering compliance training/updates.
• Build and nurture strong cross-functional relationships (MSLs, Medical Information, Regulatory Affairs, Regional & Global teams, Brand, and Commercial).

Required Qualifications & Experience

• BSc (or higher) with experience in the pharmaceutical industry or a related agency (medical communications/medical education).
• Strong project management skills with the ability to simplify complex medical messages.
• Proactive, solutions-oriented, and an excellent communicator with a collaborative mindset.
• Solid understanding of ABPI/PMCPA Code of Practice and medical governance.

This role offers a fantastic opportunity to grow your career within a highly visible position, work closely with senior stakeholders, and gain hands-on experience across the breadth of medical affairs.

For more information, please contact Julia Day at or

Role: (Senior) Scientific Director

Location: UK (Hybrid – Manchester/Macclesfield/London)

About Us

Established in 2005, Bioscript Group has developed an outstanding reputation as a high-quality strategic partner to its pharmaceutical clients, providing support with regulatory submissions, market access strategy, clinical publications, medical education and commercialisation. We work collaboratively across functions and capabilities, sharing ideas and outputs to inform each other’s work and to learn from each other’s experience; providing many opportunities for personal and professional development.

The Opportunity

We are currently looking for a Scientific Director to be at the forefront of leading and implementing our scientific and strategic vision within our medical communications division. You will be required to provide strategic leadership (technical and scientific) of editorial teams with shared responsibility for driving the success and growth of key accounts. As a senior member of the team, our Scientific Director will also provide internal leadership and strategic planning for account growth.

Key Responsibilities

• Collaborating proactively with cross-functional teams to evaluate and leverage scientific advances that drive new business opportunities
• Overall accountability and leadership across key accounts to deliver exceptional scientific quality through clear, concise, compliant and accessible content
• Ensuring adherence to industry guidelines and regulatory standards
• Working closely with the med comms leadership team to implement company objectives
• Management of designated line reports as required

About You

• Established Scientific Director looking for a new challenge with increased responsibilities and senior leadership
• Flair for business development and an appetite for driving growth
• Confident presentation skills and evident leadership skills with a passion for communicating complex ideas backed up with strong customer focus
• Meticulous attention to detail and the ability to distil complex information for diverse audiences
• A proactive approach to learning and staying informed about industry trends
• Enthusiasm for working in a collaborative and dynamic environment

Please note, this role may require domestic and international travel.

Our people are at the heart of our business

We are focused not just on delivering the exceptional for our clients, but for our teams too. We understand that everyone is different, and we believe in treating everyone as an individual with opportunities to develop your skills and career around our disciplines.

Our benefits include:

• Salary which aligns with your experience and skillset
• 25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
• Enhanced sick and compassionate leave
• Enhanced maternity, paternity & adoption leave
• Birthday charity donation to a charity of your choice
• Bonus Day off to be spent giving back to the community
• Life Insurance and Critical Illness cover
• Private Medical (Vitality for UK-based colleagues)
• Health cash plan or wellbeing allowance
• International Employee Assistance Program

We are committed to creating an inclusive and diverse workplace. We encourage applications from all individuals who meet the minimum requirements of the role. If you require any reasonable adjustments during the application or interview process, please contact us via or by calling .

Accelerating Life-Changing Solutions to Global Healthcare Challenges is the vision that unites us through a shared sense of purpose, whatever the role.

It speaks to the significant challenges that exist within global healthcare, and how we, as one team, can help to deliver better solutions and outcomes for our partners and for patients everywhere, sooner. Your job description outlines the important role and responsibilities that you own in achieving this vision.

Importantly too is how we go about living our vision.  This is defined by the Prime mission:

Through a pioneering fusion of the finest expertise in science, strategy, evidence, technology and creativity we deliver the world-class outcomes that our global partners trust to achieve their goals.

It speaks to collaboration and to everyone’s responsibility to bring together the diverse expertise that exist across our team to deliver world-class outcomes.

On this foundation, we have defined four core values, these represent the shared principles that guide our behaviours every day, whatever your role:

Be Brave, Be Human, Be Passionate, Be Exceptional. 

At Prime these values are integral to who we are.  They are there to guide you in your role and support you on your personal journey to success.  They shape our culture and support us in achieving our vision together, as one global team.  

The role

The Scientific Director at Prime plays a strategic leadership role, overseeing scientific teams to ensure the highest standards of content delivery, project execution, and client engagement within a medical communications setting. This role involves leading and mentoring scientific and editorial staff, maintaining quality and compliance with agency SOPs, and contributing to the development of strategic communication materials across therapeutic areas. The Scientific Director is responsible for fostering client relationships, supporting financial and resource planning, driving organic growth, and identifying new business opportunities. A strong scientific background (PhD, PharmD, or MD), extensive medical communications experience, and proven leadership, project management, and commercial skills are essential for success in this position.

Requirements

• PhD, PharmD, or MD
• At least 6 years’ med comms experience with a proven track record in leading scientific teams within a medical communications agency or pharma company
• Extensive medical writing experience from a medical communications or pharma environment across a broad range of projects and therapeutic areas
• Involvement in a large range of different types of projects, including  onsite and client meeting experience
• Understanding of strategic planning process
• Comfortable presenting to clients, with good presentation skills
• Some experience in developing and presenting new business proposals/pitches preferred
• Excellent communication skills
• Line management/mentoring and reviewing experience in a medical communications agency
• Strong leadership and motivational skills
• Commercial awareness relating to the financial management of a medical communications business
• Maintain a good working knowledge of the computer software required, e.g. Word and PowerPoint

Benefits

• 33 days annual leave
• Birthday day off
• 5% pension contribution
• Private medical health insurance
• WORKsmart - allows employees to have flexibility around their start and finish time
• Hybrid working