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Regulatory Affairs Officer - Pharmaceuticals & Medical Devices - Hull

Are you a Regulatory Affairs professional with a keen eye for compliance and a passion for bringing life-changing products to market? Smart4 Sciences partnering with a well-established pharmaceutical company who are looking to add a Regulatory Affairs Officer to their growing team.

About the Role:

As the Regulatory Affairs Officer, you'll play a critical part in ensuring regulatory compliance across UK, EU, and international markets. From product registration to post-market vigilance, you'll support the full lifecycle of innovative pharmaceutical and medical device products.

Key Responsibilities:

Compile and submit regulatory dossiers (new registrations, variations, renewals, CTAs).

Maintain current knowledge of MHRA, EMA, FDA, UK MDR 2002, and EU MDR 2017/745 requirements.

Liaise with regulatory bodies to resolve queries and secure timely approvals.

Manage post-market surveillance, change controls, and regulatory impact assessments.

Approve labelling and packaging for regulatory compliance.

Maintain regulatory databases and technical documentation.

What You'll Need:

Degree in a scientific discipline, chemical engineering or similar (or equivalent experience).

2+ years of regulatory affairs experience in pharma or medical devices.

Strong understanding of GMP, GDP, and ISO 13485.

Analytical mindset with excellent communication and problem-solving skills.

Experience influencing stakeholders and working cross-functionally.

Ready to take the next step in your regulatory career?
Apply now or contact Gareth Gooley on at Smart4 Sciences for a confidential conversation.

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Technology Development Lead - Wellness & Innovation - Northampton

Sector: Fragrance, Sensory Science, Biomedical Technology

A leading global organisation is seeking a forward-thinking professional to drive the development of pioneering wellness technologies at the intersection of fragrance, bioscience, and consumer well-being.

This strategic role centres on advancing a cutting-edge platform that explores the link between scent, emotion, and physiological response. You'll be responsible for shaping and executing new technology initiatives-from concept through to commercial rollout-working with a diverse team of experts and international stakeholders.

Key Responsibilities:

Develop and lead the strategy for next-generation wellness technologies.Evaluate emerging scientific and technological trends for potential application.Manage cross-functional teams through the R&D and delivery pipeline.Oversee human studies and testing related to fragrance and wellness outcomes.Collaborate with external partners and research institutions.Translate findings into commercial opportunities and market-ready innovations.

What We're Looking For:

Background in neuroscience, biomedical engineering, sensory science or similar.Hands-on experience with biosensors or biomedical devices.Strong track record in R&D and innovation, ideally within wellness or fragrance sectors.Skilled in statistical analysis, consumer research, and data interpretation.Strong communication, leadership, and project management capabilities.An entrepreneurial mindset with attention to scientific and commercial detail.

This is a unique opportunity to shape the future of scent and science. Candidates can be based anywhere globally, provided local compliance with operational presence.

If interested in this Technology Development Manager role then please send me a word version of your CV!!

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Regulatory Technologist - Cosmetics - Cheshire

Would you like to work as a Regulatory Technologist for a global leader in cosmetics? This is a great opportunity to work for a market leader in cosmetics and personal care. As a Regulatory Technologist, you will have further career progression opportunities as the business is recording year on year growth. You will be working with a dynamic company and trendsetter in the market who have created their own brand. The successful Regulatory Technologist will have the chance to build technical knowledge and a diverse professional network.

The role:
The regulatory team focuses on ethical consumer trends.
Raw materials are reviewed for cruelty free compliance, plastic-free vegan suitability and sustainability
Ensuring that processes are followed with documentary evidence supporting the marketing of cosmetics for global markets
Working closely with the NPD and Lab teams
Communicating with testing houses, raw material suppliers and regulatory bodies.

Ideal requirements:
Previous cosmetics or relevant regulatory experience - (graduates will be considered)
Computer literate, knowledge of the MS Office suite.
Ability to work independently and as part team in a fast-paced environment
Ideal candidates would come from a BSc/MSc Cosmetic Science or a Chemistry background


If you are interested in this Cosmetics Regulatory Technologist role please send me a word version of your CV!!

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Manufacturing Engineer- Pharmaceutical/ Medical Device

I am working with a pharmaceutical/ Medical Device manufacturing site based in Liverpool specialising in Single-Use Technology (SUT) manufactured in a sterile environment. Your will be responsible for defining the manufacturing & inspection process, for single use components. Very exciting time to start as the development of the product has now moved into manufacturing.

Key responsibilities for the Manufacturing Engineer- Pharmaceutical/ Medical Device

Design, implement, and validate single-use assemblies and systems for internally manufactured parts.Investigate any issues within the manufacturing process and create and implement corrective and preventive procedures.Author and review technical documentation, including protocols, SOPs, and engineering reports.Work closely with technicians in the clean room, providing technical support for the manufacturing process, this can be daily at times.Ensure compliance is met within manufacturing to ISO standards.

Requirements for the Manufacturing Engineer- Pharmaceutical/ Medical Device

Bachelor's degree in engineering (Mechanical, Chemical, Bioprocess, or related field).Good understanding of ISO programming.Strong understanding of CAD Modelling, CMM Equipment and CAM Programming.Experience in GMP, ISO, validation protocols, and cleanroom practices.Strong expertise in Single-Use Components, such as bags, tubing, filters, and connectors.

Benefits for the Manufacturing Engineer- Pharmaceutical/ Medical Device

25 holidays per year + Bank HolidaysChristmas shutdown.Cycle to work schemeIncome Protection schemeLife Assurance 4x salaryEarly finish on a Friday and flexible working hours.

To apply for the Manufacturing Engineer- Pharmaceutical/ Medical Device or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email me at

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QA Manager - Pharmaceutical Manufacturing
Northamptonshire | Competitive Salary + Benefits | Permanent, Full-Time

Are you an experienced QA professional ready to take the next step in your career? Smart4 Sciences are working with a leading pharmaceutical manufacturing company in Northamptonshire that's on the lookout for a skilled QA Manager to join their growing team.

This is a fantastic opportunity to take ownership of the Quality Assurance function on a busy GMP site, support a collaborative and quality-driven culture, and help shape the future of pharmaceutical manufacturing.

The Role:

As QA Manager, you'll lead a small but experienced QA team and take responsibility for the site's QMS, GMP compliance, and internal audit programme. You'll work closely with production, QC, and supply chain teams to ensure products meet regulatory standards and are released efficiently, working alongside the QP.

This is a hands-on leadership role in a company that values continuous improvement and employee development.

What You'll Be Doing:

Managing and mentoring the QA team

Leading GMP compliance across manufacturing and packaging operations

Owning and developing the Quality Management System

Hosting and supporting audits (MHRA, client, internal)

Overseeing deviations, CAPAs, change controls, and batch review

Working cross-functionally to drive quality improvements

What We're Looking For:

Solid QA background in pharmaceutical manufacturing

Proven experience managing or leading a QA team

Strong knowledge of EU GMP and GDP regulations

Comfortable leading audits and interfacing with regulatory bodies

A science degree (or equivalent experience) is preferred

Why Apply?

Be part of a forward-thinking and supportive company

Take ownership of quality strategy and improvements

Enjoy a stable, permanent position with real development prospects

Interested?
If you're a passionate QA professional looking for a new challenge in the Northamptonshire area, we'd love to hear from you.
Apply today or contact Gareth Gooley on for a confidential chat about the role!

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Technology Transfer Lead - Permanent - Humberside

** Lead Tech Transfer Projects for a Pharmaceutical expansion **

Are you a degree qualified chemical process engineer OR graduate in Pharmaceutical Sciences ?

Do you have expertise in ...

Pharmaceutical Formulation Development Process Development Scale up Technology Transfer

If you do & you would like the chance to join an expanding pharmaceutical organisation in the second phase of growth ...

Please apply now to Simon Fowler at NGAGE Smart4Sciences on 01925239725

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QA Manager / RP / RPi - Pharmaceuticals - Greater London Area

Are you an experienced Quality Assurance professional with RP and RPi eligibility, looking for your next challenge in a dynamic and expanding pharmaceutical company?

Our client, a rapidly growing and innovative pharmaceutical business based just outside London, is seeking a QA Manager who is also eligible to act as the Responsible Person (RP) and Responsible Person for Import (RPi) under GDP regulations. This is a hybrid role with excellent development prospects and the chance to make a significant impact in a highly collaborative team environment.

Key Responsibilities:

Oversee and continuously improve the company's Quality Management System (QMS)

Act as the Responsible Person (RP) and RPi, ensuring full compliance with GDP and MHRA expectations

Maintain and manage supplier and customer qualification processes

Lead audits (internal and external) and host regulatory inspections

Provide QA leadership across all GxP activities related to the import, storage, and distribution of medicinal products

Train, mentor, and develop QA staff

Support strategic projects including new product launches and licensing expansions

Requirements:

Eligibility to act as RP and RPi (MHRA named or ready to be named)

Strong background in pharmaceutical QA within a GDP/GMP environment

Excellent knowledge of EU GDP and UK regulatory expectations

Importation experience highly desirable

Personable, pragmatic, and proactive approach with great attention to detail

Prior experience working with a WDA(H) and MIA(IMP) license is a strong plus

What's On Offer:

A competitive salary and benfits package

Hybrid flexibility with a site located just outside London

Opportunity to grow with the business as it scales operations

🔍 Interested in learning more?
Apply now to take the next step in your QA career, or reach out confidentially to Gareth on for more information

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Contract Analyst - Method Validation - Bristol - 4-6 Month Contract

*** Urgent Vacancy to support method validation for a new generic tablet formulation ****

Do you have experience in method validation for HPLC methods for products registered under MHRA/GMP ?

Are you skilled in report writing & protocol generation for HPLC & dissolution testing methods ?

Are you immediately available for a new contract ?

Please apply now or contact Simon Fowler at NGAGE Smart4Sciences on 01925239725 or to process your application

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QA Officer - Pharmaceutical Manufacturing - HULL

Join a Growing Pharmaceutical Company with a Passion for Quality and Innovation!

We are partnering with an ambitious and rapidly expanding pharmaceutical manufacturing company based in Hull to recruit a QA Officer. This is an exciting opportunity to be part of a company making significant investments in their facilities, people, and future.

As a QA Officer, you'll play a vital role in ensuring that quality standards are upheld across all stages of manufacturing and supply. Whether you're an experienced QA Associate looking to take the next step, or already operating as a QA Officer, this role offers the chance to grow in a supportive and collaborative environment.

Key Responsibilities:

Support the implementation and maintenance of the Quality Management System (QMS) in line with GMP and regulatory requirements.

Conduct batch record review and assist in product release activities.

Handle deviations, CAPAs, change controls, and customer complaints.

Assist with internal audits and regulatory inspections.

Support document control processes and SOP management.

Collaborate with manufacturing, QC, and supply chain teams to promote a culture of continuous improvement.

Ideal Candidate Profile:

Prior experience in a GMP-compliant pharmaceutical environment, ideally within a CDMO.

Strong understanding of pharmaceutical quality systems and regulatory guidelines.

Excellent attention to detail and communication skills.

Ability to work both independently and as part of a team.

Science degree or relevant qualification preferred.

Why Join?

Be part of a growing business with exciting expansion plans.

Modern facilities and a forward-thinking team.

Genuine opportunities for progression and development.

Competitive salary and benefits package.

Positive, quality-driven culture.

Ready to take your QA career to the next level in a company that's going places?
Apply now or contact Gareth Gooley on for more info

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Qualified Person (QP) - Sterile Manufacturing

Are you a Qualified Person with experience in sterile pharmaceutical manufacturing? Looking to make an impact in a forward-thinking company where quality and patient safety come first?

Smart4 Sciences are working with a pharmaceutical manufacturer in Essex specialising in the production of sterile and non-sterile products. As part of their continued expansion, they're seeking an experienced and proactive Qualified Person to join their quality team.

The Role:

As a QP, you'll be responsible for ensuring that products released to market meet the highest standards of GMP compliance and patient safety. Working in a modern GMP facility, you will:

Act as a QP for the certification and release of sterile pharmaceutical products

Ensure full compliance with MHRA and EU GMP guidelines

Liaise closely with QA, Production, and Regulatory Affairs teams

Contribute to audits, inspections, and continuous improvement projects

Support the development of junior QA staff and provide QP oversight where needed

About You:

Eligible to act as a Qualified Person under Directive 2001/83/EC

Prior experience working with sterile manufacturing (aseptic/terminally sterilised products) is desirable

Strong working knowledge of EU GMP and UK pharmaceutical regulations

If you're a QP ready for your next challenge in a state-of-the-art sterile manufacturing environment, we'd love to hear from you!

Apply today or contact Gareth Gooley on for a confidential discussion.

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