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GMP Recruitment are proud to be partnered with a highly successful and well-known manufacturing business located in Pershore. We are currently recruiting for an experienced Technical Author to join their team on a full time, permanent contract, to independently produce high-level documentation. You will work hands-on with the machinery to translate complex engineering into clear, accurate manuals and qualification packages.

This position is office based, working Monday Friday 08:00am 16:30pm offering a salary of up to £40,000 which will be pending relevant, previous experience.

Technical Author main duties:

• Producing full documentation packages (Manuals, IQ/OQ, SDS, HDS, DQ, and FDS).
• Working directly with physical machinery to ensure documentation accuracy.
• Contributing to the department to help streamline documentation processes.
• Ensuring all documentation meets required industry standards.

Technical Author required skills and experience:

• Minimum 3 years in a technical authoring role with a technical or automation background.
• Proficient in Microsoft Office; excellent written English and communication skills.
• Organised, attentive to detail, and a desire to pursue a career in engineering.
• Taking care of the company and customers as though they were your own.
• Pursuing new ideas and listening to creative suggestions.
• Encouraging initiative and adopting a well-managed environment.
• Working together with respect to achieve results without conflict.

This is a remarkable opportunity for a passionate and driven professional to contribute to the success of world-leading manufacturing business.

If this job sounds ideal for you, then do not miss out and apply NOW!

GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency.

Temporary Medical Secretary, Little Hulton Immediate start (Ongoing)

13 - 14 per hour, Mon-Fri - 27 hours per week.

Our client is looking for an experienced Medical Secretary to support their team.

Duties will be:

• Audio typing patient letters and documents
• Answering incoming calls
• Maintaining records on EMIS
• Supporting both inpatient and outpatient departments with administrative duties
• Minute taking in meetings

Previous experience with audio typing, minute taking and using EMIS is essential for this role.

Please note that this role will involve discussing and typing sensitive content that some people may find upsetting.

Due to the high volume of applications we receive, only those successfully shortlisted for the role will be personally contacted.

Follow FORREST RECRUITMENT LTD on LinkedIn and Facebook for updates, recruitment information, new vacancies and more!

Medical Secretary Ad Hoc Holiday & Sickness Cover (Bank Staff)

We are looking to build a bank of experienced Medical Secretaries who are available to provide ad hoc holiday and sickness cover for our client, based in Epsom.

• Approximately 2 hours per day, 6 days per week
• Minimum 1 day per week onsite at their Epsom clinic
• Remaining hours can be worked remotely, where appropriate

Requirements:

• Previous experience in medical administration is essential
• Excellent organisational and communication skills
• Ability to work independently and manage confidential information
• Experience within mental health services would be advantageous

Rate of Pay:

• 15 - 20 per hour, depending on experience

This is an excellent opportunity for a flexible and reliable Medical Secretary looking for additional work on an ad hoc basis.

If this could be of interest, please send your CV and a brief summary of your availability.

Refer a friend and earn a retail voucher worth up to 500!

Unfortunately, due to high numbers of applications, we are only able to respond to shortlisted applicants. If you have not heard from us within 5 days, please assume that you have not been shortlisted on this occasion.

By applying for this vacancy, you accept Lloyd Recruitment Services Privacy and GDPR Policy which can be found on our website and therefore gives us consent to contact you.

Lloyd Recruitment Services are acting as a recruitment agency in relation to this vacancy and are an equal opportunities employer

ME15710

Are you an experienced Medical Secretary with excellent medical knowledge?

Have you used ERS and able to do medical reports and insurance?

Are you immediately available?

If you can answer yes to all of the above, Lifeline has a brilliant opportunities for you!

A welcoming NHS GP surgery is looking for a Medical Secretary to work part time Monday - Wednesday.

The ideal Medical Receptionist will:
Have at least 6 months recent experience working in NHS GP surgery as a Medical Secretary
Be confident in using ERS and Emis Web
Have Your Own Smart Card
Be happy to undergo a DBS check or have a DBS certificate dated within a year
Be flexible, reliable and professional

Lifeline Recruitment Services is a specialist NHS approved health care agency, who are the preferred supplier to a variety of GP Practices and Private Clinics all over the UK.

Here at Lifeline, we pride ourselves on our dedicated service for both candidates and clients. Our friendly staff ensure that you experience a smooth registration process, are committed to finding you the right shifts and can be easily contacted.

Join us and start your new locum career today!

Registering with Lifeline guarantees you:
Excellent pay rates
Suitable locations
Quick and easy registration
Weekly email job alerts

If you are interested please apply for the role now,

Medical Secretary Ad Hoc Holiday & Sickness Cover (Bank Staff)We are looking to build a bank of experienced Medical Secretaries who are available to provide ad hoc holiday and sickness cover for our client, based in Epsom.

• Approximately 2 hours per day, 6 days per week
• Minimum 1 day per week onsite at their Epsom clinic
• Remaining hours can be worked remotely, where appropriate

Requirements:

• Previous experience in medical administration is essential
• Excellent organisational and communication skills
• Ability to work independently and manage confidential information
• Experience within mental health services would be advantageous

Rate of Pay:

• £15 - £20 per hour, depending on experience

This is an excellent opportunity for a flexible and reliable Medical Secretary looking for additional work on an ad hoc basis.If this could be of interest, please send your CV and a brief summary of your availability.Refer a friend and earn a retail voucher worth up to £500!Unfortunately, due to high numbers of applications, we are only able to respond to shortlisted applicants. If you have not heard from us within 5 days, please assume that you have not been shortlisted on this occasion.By applying for this vacancy, you accept Lloyd Recruitment Services Privacy and GDPR Policy which can be found on our website and therefore gives us consent to contact you.Lloyd Recruitment Services are acting as a recruitment agency in relation to this vacancy and are an equal opportunities employerME15710

Are you a chemical regulatory professional within the cleaning / hygiene chemical sector?

Looking for a remote role with just the occasional trip to head office in Scotland?

Or are you looking for an onsite or hybrid role?

This may be for you

A growing manufacturer using a unique and sustainable approach to cleaning and personal care products are looking for a seasoned regulatory professional to join their team.

Reporting into the technical director, you'll have experience within the cleaning / hygiene / personal care sector, you'll be experienced with biocidal, cosmetic and REAH regulations and you'll have a problem solver mentality, with the ability to question problems and come up with solutions.

What you will do:

• Advise on and, enforce, the company's compliance with all relevant National and International Regulations, with respect to product claims and marketing text, for all of the company's products and their respective market sectors.
• Assist in the creation of product labels, online and offline marketing material and, responses to customer enquiries relating to compliant product claims.
• Communicate, on behalf of the company, with any and all relevant statutory and regulatory authorities, both Nationally and Internationally, for the purpose of establishing compliance and, where required, achieving registration, approval and/or certification etc.
• Oversee the compliance of Safety Data Sheet text.
• Support where appropriate, the sales and marketing activities of the company.
• Attend such meetings as required.

What you will need:

• Highly desirable Previous experience with the UK and EU Biocide, Detergent, Cosmetic and CLP Regulations.
• Competent verbal and written communicator.
• Proven ability in extracting important information from regulatory waffle.
• Quick learner, able to gather and assimilate information quickly and effectively.
• Desirable - Experience with Canadian and USA regulations.
• Probably educated to degree level or equivalent, but this is not a prerequisit.
• Organised.
• Happy to work alone or as a team member.

Talentmark are recruiting for a Regulatory Labelling Specialist to join a leading pharmaceutical company on a 12-month contract.

Salary:
21.10 per hour PAYE, or 27.63 per hour Umbrella.

Regulatory Labelling Specialist Role:

• Prepare and update labelling documents for assigned markets.
• Produce regulatory submission documents and complete QC checks.
• Support responses to health authority and inspection queries.
• Contribute to digital and automation improvement projects.

• A degree in life sciences, pharmacy or a related field, or equivalent experience.
• Knowledge of pharmaceutical labelling and regulatory requirements.
• Confident with Excel, SharePoint or similar tools.
• Strong attention to detail and clear written communication.
• Fluent in English. German or French is a bonus.

Regulatory Affairs Coordinator

Hertford

Hybrid/Part-Time Working Available

Up to 40,000

An established manufacturer of regulated products is seeking a Regulatory Affairs Coordinator to support the ongoing maintenance of compliance and technical documentation across an established portfolio of products.

This is a hands-on role suited to someone who enjoys practical regulatory work within an SME environment and can efficiently manage documentation and compliance activities without unnecessary complexity.

• Maintain UK and EU product registrations.
• Review and maintain Technical Files and supporting documentation.
• Prepare and maintain PMS, PSUR and Clinical Evaluation documentation.
• Review and update IFUs and product labelling.
• Monitor regulatory updates and ensure ongoing compliance.
• Prepare technical justifications, gap analyses and briefing notes.
• Support customer regulatory queries and external audits.
• Maintain electronic and physical document control systems.

• Previous experience within medical devices, regulatory affairs or quality assurance.
• Knowledge of ISO13485 and medical device regulations including MDR, MDD and UKCA.
• Experience with Technical Files and technical documentation.
• Strong organisational skills and attention to detail.
• Comfortable working independently within an SME environment.

Unfortunately, sponsorship is not available for this position, so applicants must already hold full and unrestricted right to work in the UK.

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business continues to invest heavily in next-generation technologies and regulatory excellence.

We have an opportunity for a Regulatory Affairs Manager to lead the EU Regulatory Strategy for a brand new Class III medical device. This is a strategically significant role within a highly experienced global regulatory function.

As the Regulatory Affairs Manager, you will define and drive the EU regulatory pathway under MDR 2017/745 for a new product programme. You will lead regulatory strategy development from early-stage development through to submission and approval, ensuring alignment with global regulatory, clinical and R&D teams.

This position is centred on regulatory project leadership rather than line management. While there is no direct people management initially, the scope and visibility of the programme offers long-term progression potential.

To be successful as the new Regulatory Affairs Manager, you will bring proven experience leading EU regulatory strategy for Class III medical devices, ideally within a structured global organisation. You will be confident defining approval pathways under MDR 2017/745, comfortable operating at project leadership level across R&D, Clinical and global Regulatory teams, and experienced in managing Notified Body interactions. You will combine technical depth with the ability to influence stakeholders, manage complex timelines and take ownership of a high-visibility regulatory programme from concept through to approval.

Key Responsibilities

• Define and own the EU regulatory strategy for a new Class III device under MDR.
• Lead regulatory project management activities, integrating with global RA, Clinical Affairs and R&D teams.
• Develop and maintain regulatory plans aligned to product development milestones.
• Lead Notified Body strategy and manage regulatory interactions.
• Provide regulatory input into design, risk management, clinical strategy and technical documentation.
• Support audits and ensure ongoing compliance with ISO 13485 and applicable regulations.

Experience and Skills Required

• Proven experience within Regulatory Affairs in medical devices.
• Direct experience with Class III devices is essential.
• Demonstrated leadership of regulatory strategy for new product development programmes is essential.
• Strong working knowledge of EU MDR 2017/745 and associated regulatory frameworks.
• Experience interacting with Notified Bodies and Competent Authorities.
• Experience across additional regions such as US or other international markets is highly desirable but not essential.
• Degree in a relevant scientific or engineering discipline.

This is a high-impact opportunity within a globally recognised organisation where regulatory strategy sits at the heart of product success. It will suit a regulatory professional who enjoys ownership, structured project delivery and operating within a large, well-resourced international environment.

If you would like to discuss this opportunity in confidence, we would welcome a conversation.

QHSE & Compliance Manager - Chemical Manufacturing

Reporting to the Head of Technical, you will lead all Quality, Health, Safety, Environmental, and Chemical Compliance activities on site. This role is focused on ensuring full regulatory compliance while promoting a strong safety-first culture, supported by an existing team.

Key Responsibilities

Quality & Compliance

• Manage and maintain the ISO 9001 Quality Management System
• Ensure product quality, traceability, and documentation control
• Lead audits (customer, supplier, certification)
• Investigate non-conformances and implement CAPA
• Support change management processes (MOC)

Health & Safety / Process Safety

• Ensure compliance with UK legislation (HSE Act, COSHH, DSEAR, COMAH)
• Lead risk assessments, hazard identification, and safe systems of work
• Oversee Permit-to-Work systems and contractor safety
• Lead incident and near-miss investigations using root cause analysis
• Deliver training, inductions, and toolbox talks
• Act as site lead for emergency response and business continuity

Environmental & Regulatory

• Maintain the Environmental Management System
• Ensure compliance with permits, waste, and emissions controls
• Monitor environmental performance and drive improvements
• Ensure compliance with REACH, CLP, and COSHH regulations
• Maintain SDS and ensure correct classification, labelling, and storage
• Liaise with regulators (HSE, Environment Agency) and support inspections
• Support new product introduction from a compliance perspective

Essential Requirements

• Experience in a QHSE role within chemical manufacturing
• Strong knowledge of UK H&S and chemical regulations
• Experience with ISO systems and audits
• Proven ability in risk assessment, incident investigation, and safety leadership
• Strong communication skills and ability to influence stakeholders
• Detail-oriented with a practical, safety-first approach
• Candidates must have the right to work in the UK indefinitely (Sponsorship is not available for this role)

Qualifications (Desirable)

• NEBOSH Certificate or Diploma
• Degree in Chemistry, Chemical Engineering, Environmental Science or similar

To apply for this QHSE & Compliance Manager position, please submit your CV and cover letter detailing your relevant experience and why you are interested in this position