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Radiation Products & Services Manager (Healthcare & Medical Technology)

UK Wide / Remote

Up to £95,000 + Car Allowance + Remote + Pension + Additional Leave + Health & Wellbeing Programme

Are you a Medical Device Sales Manager, Radiology Specialist, Healthcare Technology Account Manager, Medical Physics Professional or similar looking to take the next step in your career with a growing specialist org click apply for full job details

Clinical Safety Scientist

Type: Temporary
Duration: 6 months initially
Location: London (hybrid working available
Rate: (INSIDE IR35) up to 500 per day (Umbrella)

We are seeking a Safety Scientist to support the safety evaluation and risk management of medicines, with a particular focus on HIV treatments and prevention. This is a critical role contributing to patient safety across the full product lifecycle-from late-stage development through to post-marketing.

Key Responsibilities

• Monitor and evaluate the safety profiles of assigned products across development and post-marketing phases
• Conduct signal detection and evaluation, including analysis of safety data and literature review
• Contribute to the development and maintenance of Risk Management Plans and regulatory safety documentation
• Support preparation of key regulatory deliverables (e.g., DSURs, PBRERs, EU RMPs, licence renewals)
• Collaborate with safety physicians on benefit-risk assessments and individual case safety reviews
• Ensure all safety documentation meets global regulatory and compliance standards

Skills & Experience Required

• Degree (BSc or higher) in Biomedical Sciences, Life Sciences, or related healthcare field
• Proven experience in clinical trial data review and pharmacovigilance activities
• Strong scientific writing skills with experience in regulatory safety documents
• Knowledge of signal detection, causality assessment, and safety data evaluation
• Experience in literature review, data analysis, and interpretation
• Understanding of pharmacovigilance regulations and drug development processes (HIV knowledge advantageous)

To Apply

Please click below and/or to discuss further, contact Theo Charles on (phone number removed)

PAYE also possible - please enquire for more information

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Technologist - Product Testing
Location: Kettering
Salary: Up to 29,000 per annum
Hours: 37.5 hours per week

About the Organisation
Our client is a well-established testing and certification organisation supporting manufacturers and suppliers worldwide. The business provides independent testing services across a wide range of products, helping customers demonstrate compliance with relevant national and international standards.

About the Department
The Product Testing team is responsible for evaluating a broad range of Personal Protective Equipment (PPE) and safety-related products to ensure they meet required performance and protection standards.
Products tested may include:
Protective gloves
Fall protection equipment
Motorcycle apparel
High-visibility clothing
Eye and face protection
Helmets
Hearing protection
Chainsaw protective clothing
Kneepads
Sports protection equipment
Other specialist protective products

The department operates accredited laboratory facilities equipped with advanced testing machinery and instruments. Test results are used to support product development, regulatory compliance, and certification requirements.
The team consists of skilled technicians, technologists, and support personnel who work collaboratively to deliver high-quality testing services to customers globally.

The Role
An opportunity has arisen for a Technologist to join the Product Testing team.
Key responsibilities include:
Conduct routine physical testing in accordance with recognised international and European standards.
Operate laboratory equipment and accurately record test data in both electronic and hard-copy formats.
Prepare technical reports detailing test results and findings.
Liaise with customers via email, telephone, and face-to-face meetings.
Respond to technical enquiries and advise customers on appropriate testing requirements.
Maintain accurate records and update job information using internal business systems.
Contribute to the continuous improvement of laboratory processes and testing procedures.
Support business development and industry engagement activities, including seminars, webinars, exhibitions, and customer visits.
Comprehensive training will be provided where required.

Candidate Profile
Essential Requirements
High level of accuracy and attention to detail.
Self-motivated with the ability to use initiative.
Logical and methodical approach to work.
Ability to work both independently and as part of a team.
Experience dealing with customers in a professional environment.
Adaptable and responsive to changing priorities.
Strong organisational, time management, and communication skills.
Good working knowledge of Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
Desirable Skills & Experience
Experience working within a laboratory or testing environment.
Knowledge of technical standards and compliance requirements.
Understanding of PPE manufacturing and performance requirements.
Experience using database or business management systems.
Familiarity with quality management systems (QMS).
Educational background in Physics or a related scientific discipline.
Experience travelling for work purposes.
Additional language skills.

Benefits
The successful candidate will have access to a comprehensive benefits package, which may include:
Generous annual leave entitlement, increasing with service.
Life assurance.
Pension scheme.
Income protection cover.
Free on-site parking.
Flexible working arrangements.

Application Information
Applications should be submitted by 24 July 2026.
Interviews are expected to take place on-site during August 2026.

Interested? Please click apply.

Talentmark are recruiting for an Associate Director, Drug Safety to join a company in the pharmaceutical industry on a contract basis for 12 months.

Salary:
67.96 - 75.51 per hour PAYE or 90 - 100 per hour Umbrella/Ltd.

Associate Director, Drug Safety Role:

• Provide safety oversight and input across the full study lifecycle, from early development through to post-market.
• Lead post-market safety work, including signal evaluation, benefit-risk assessment and risk management.
• Own case reporting, including aggregate reports such as DSUR and PBRER.
• Drive signal detection and contribute to the strategic review of safety reports.
• Prepare and maintain risk management documents, including CCDS, labelling documents, RMPs and REMS.

• Strong understanding of GxP, regulated processes and the clinical trial lifecycle.
• Confident communicator, able to work with remote teams across different countries.
• Skilled in data analysis and statistical methods, with the ability to present findings clearly.
• Strong presenter, able to summarise key points for different audiences.
• Able to work independently with minimal supervision.
• A postgraduate qualification in a life sciences field (PhD, MSc, medical or PharmD) is preferred but not essential.

Scientist II - Physical Testing
Location: Deeside, UK
Contract Type: Contract (12 Months)
Start Date: ASAP
Pay Rate: 142.32 per day (PAYE)

About the Role
We are seeking a Scientist II to join our Technology & Innovation team at our Global Development Centre in Deeside. This is an excellent opportunity for a scientifically minded professional to contribute to the stability testing of medical devices and skincare products, supporting product shelf-life claims, regulatory compliance, and product labelling requirements.
The successful candidate will perform physical and analytical stability testing in accordance with established study protocols, SOPs, quality standards, and regulatory requirements. Working within a GMP/GLP laboratory environment, you will play a key role in generating, analysing, and reporting stability data while contributing to continuous improvement initiatives across the laboratory.

Key Responsibilities
Stability Testing & Analysis

• Perform physical and analytical stability testing on existing and new medical devices and skincare products.
• Analyse, interpret, document, and report laboratory data to GMP/GLP standards.
• Collate stability data and support the generation of technical and stability reports.
• Assist in the preparation of shelf-life plans, stability protocols, and associated reports.
• Suggest appropriate real-time and accelerated ageing programmes for study concepts.
• Coordinate and organise stability studies from initiation through to completion.
• Support planned and ad hoc stability sample set-downs and pull requests.

Laboratory Operations

• Maintain, calibrate, and support laboratory equipment while ensuring quality records remain up to date.
• Work confidently with a broad range of analytical instrumentation, including balances, pipettes, HPLC, and ICP-MS.
• Support storage and retrieval activities for stability samples.
• Assist with maintenance, servicing, and calibration activities completed by external suppliers.
• Monitor laboratory inventory levels and request replenishment of consumables, chemicals, and reagents as required.

Quality & Compliance

• Maintain compliance with ISO 13485, ISO 9001, GMP, and GLP requirements.
• Draft and maintain stability documentation, including protocols and reports.
• Prepare quality documentation such as Change Controls, Non-Conformances, and Out of Specification (OOS) reports.
• Participate in laboratory investigations and support root cause analysis and troubleshooting activities.
• Provide timely support during internal and external audits.
• Ensure laboratory activities comply with site Health & Safety, environmental, and quality procedures.

Continuous Improvement & Team Support

• Support ongoing improvements to stability testing processes and operating procedures.
• Actively participate in Lean and 6S initiatives within the laboratory environment.
• Train and support new or less experienced team members on test methods, equipment use, and calibration procedures.
• Promote a safe working environment and raise near misses where appropriate.
• Provide technical input into stability studies under the guidance of senior scientists.

About You
To be successful in this role, you will be a detail-oriented scientist with experience working within a regulated laboratory environment. You will possess strong analytical skills, a commitment to quality, and the ability to effectively manage multiple priorities in a fast-paced setting.
Essential Skills & Experience

• BSc degree (or equivalent) in a scientific discipline such as Chemistry, Biology, or a related field.
• 1-2 years of experience within the Medical Device, Pharmaceutical, or related Life Sciences industry, ideally in an R&D or product development environment.
• Experience following laboratory procedures, protocols, SOPs, and technical documentation.
• Knowledge of GMP, GLP, and quality management systems.
• Understanding of FDA, ICH, and European regulatory requirements.
• Experience using laboratory analytical equipment and instrumentation.
• Strong written and verbal communication skills.
• Proficiency in Microsoft Office, particularly Word and Excel.
• Experience using computerised systems for data management and record keeping.
• Excellent organisational skills with the ability to prioritise changing workloads.
• Positive, proactive attitude with a continuous improvement mindset.

Desirable Experience

• Experience working with HPLC and ICP-MS instrumentation.
• Exposure to stability testing programmes within medical device or pharmaceutical development.
• Experience participating in audits and laboratory investigations.

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Title: CDM & Health & Safety Lead

London Hybrid Working

Salary: Up to £65,000 + £5,000 Car Allowance + Bonus + Comprehensive Benefits

Lead. Influence. Grow.

Are you an experienced CDM and Health & Safety professional looking for a role where you can genuinely shape a regional service, influence business strategy and progress into senior leadership?

Carriera has been exclusively retained by one of the click apply for full job details

Adecco Worcester are recruiting on behalf of a client for an opportunity to join a growing design, import, and distribution business supplying consumer products across the UK and Europe. This role takes full ownership of product compliance, safety, and testing across a varied product range sold through retail and online channels, including Amazon.

Key Responsibilities

• Lead and manage all product compliance and regulatory activities
• Ensure products meet UK & EU legislation (GPSR, CE/UKCA, REACH, RoHS, etc.)
• Develop and oversee testing and certification programmes
• Liaise with external test houses (e.g. SGS, Intertek, T V)
• Review test reports and maintain technical documentation
• Support product development and advise suppliers on compliance requirements
• Manage Amazon and marketplace compliance, including documentation requests
• Conduct risk assessments and support product safety investigations or recalls
• Maintain audit-ready records including Declarations of Conformity and technical files

Skills & Experience

• 5+ years in product compliance, testing, or product safety
• Strong knowledge of UK/EU regulations and standards
• Experience managing testing programmes and reviewing reports
• Background working with overseas suppliers
• Highly organised with strong attention to detail

Desirable

• Experience with testing bodies or marketplace compliance (e.g. Amazon)
• Background in consumer goods

What Success Looks Like

• Compliant product launches with no delays
• Strong testing and certification processes
• Reduced compliance risk across retail and online channels

Please contact Gemma at Adecco today if you would like to know more!

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

You ll be testing the integrity of critical component parts of aircraft

Using digital x-ray devices to ensure there are no cracks, flaws or fractures, this naturally requires your absolute attention to detail

Other tasks include undertaking helium gas leak detection and penetrating dye inspection of machined components

You need Level 1, Level 2 or Level 3 NAS410 or EN 4179 or equivalent, experience in NDT quality control and inspection, preferably in the aerospace, automotive, nuclear, rail or medical device engineering sector including the analysis of film or digital x-ray images.

This is a daytime shift working 8.00am to 4.45pm Monday to Thursday and 8.00am to 12.00 midday Friday. Flexible hours and overtime available

In return you ll be part of a quality team dedicated to the production of rocket propelled aircraft equipment systems used in a very unusual application You ll easily be the most interesting person down at the pub

CV not ready? No problem, just email, text, WhatsApp or call me I ll always get back to you

Our Client is looking to recruit a Drug Safety Administrator to join their team

This is a Technical Role for persons with a life science degree, degree in pharmacy and nursing qualifications. For this title, the Drug Safety Administrator desirable to have at least 1 year of experience as a Drug Safety Administrator or can be a recent graduate. The Drug Safety Administrator shows an understanding of the Quality Management Process with a good knowledge and understanding of applicable company policies, procedures and working practice documents.

KEY RESPONSIBILITIES & TASKS

• For scenarios or projects that fall outside the scope of their technical, clinical or medical expertise should be escalated or in certain circumstances pre-checked by a senior or more technically qualified colleague before final release.
• Keeping the Pharmacovigilance Manager fully informed of problems and issues that may arise related to the product, adverse events, the patients, prescribers or the marketing authorisation holder.
• In the absence of Drug Safety Associate, the Drug Safety Administrator escalates these issues to a senior or more technically qualified staff member for their clinical input and guidance, as required.
• Upload ProQuest alerts for assigned active ingredients into the Literature Monitoring System (LMS). Identifying case reports and important safety information/published studies in the LMS database.
• Processing selected case reports in the ICSR database.
• Checking all literature case reports have the appropriate AE terms assigned for MedDRA coding. Notifying the QPPV of cases where the appropriate MedDRA term cannot be identified independently.
• Reconciliation both with clients and/or with PV partners on behalf of clients (as required).

Screening of Published Literature & the MLM Service

Individual Case Safety Reports

• Processing ICSR reports from any source in the drug safety database.
• Attaching source documents with each case on the drug safety database.
• Exchanging a PV case reference from the ICSR database and exchanging these with PV partners.
• Conducting follow up investigation for direct reports from either patients or healthcare professionals. Exchanging a PV case reference from the ICSR database and exchanging these with PV partners.
• Conducting follow up investigation for direct reports from either patients or healthcare professionals.

Qualifications

The ideal person will must have a Life Science Degree either a recent graduate looking to secure their second job, or has a nursing degree or experience

Please note only CV s with these qualifications or experience will be considered.

Has a life science degree and is either a recent graduate or looking to secure their second job.

Candidates must be located within commuting distance of either Bedfordshire, Buckinghamshire, or Northamptonshire.

Role Overview

We are seeking a highly motivated Senior Technologist to support the development and optimisation of e-liquid products within our laboratory and pilot plant environments. This role plays a key part in driving continuous improvement in product quality, safety, and innovation as part of our next-generation vaping product strategy.

You will contribute to formulation development, support product development processes, and collaborate with cross-functional teams to ensure high-quality outcomes. This role combines hands-on laboratory work with data analysis, reporting, and stakeholder engagement.

• Develop and prepare e-liquid formulations to address technical challenges and support continuous product improvement.
• Conduct routine laboratory testing using standard analytical techniques (e.g., pH, density, viscosity, NIR, UV-Vis, flash point).
• Produce, review, and summarise experimental and production data to support decision-making.
• Plan and manage short- and long-term formulation requests, using structured project management approaches where needed.
• Collaborate with internal teams including Product Development, Sensory, Analytical Science, Quality, and Compliance.
• Maintain laboratory equipment, including calibration and routine maintenance.
• Ensure all work complies with safety, environmental, and quality standards, including appropriate use of PPE.
• Support quality systems, including ISO standards and audit readiness.
• Follow and promote best practices in laboratory operations, data management, and reporting.

• Proven laboratory experience, including sample preparation and analytical testing.
• Strong planning and organisational skills, with the ability to prioritise effectively.
• A curious mindset with strong problem-solving capabilities.
• Excellent communication and interpersonal skills.
• Ability to collaborate effectively across multidisciplinary teams.
• Detail-oriented with a structured and methodical approach to work.
• Comfortable working independently and under pressure in a fast-paced environment.

• Bachelor's degree (BSc or equivalent) in Chemistry, Biochemistry, or a related scientific discipline.

• Experience in e-liquid formulation or similar product development.
• Knowledge of product quality testing and analytical techniques.
• Experience handling hazardous materials and preparing small-batch samples.

This is a temporary position initially until the end of 2026 but with a strong likelihood of extension.

Pay: 17.89 - 18.51 per hour (PAYE)