12 jobs in The IVF Guide

The IVF Guide in South Wales is seeking a senior IVF nurse to join a busy clinic delivering around IVF cycles across two sites and providing outstanding patient care.

You will bring registered nurse expertise in IVF/ART, perform scanning, support prescribing where appropriate, and work with a dedicated team in a fast-paced environment in Swansea. This role offers opportunities to contribute to patient journeys with strong clinical support.

Nurse Manager (Fertility) – North East England, UK

Permanent | Full-time

Our client is one of the UK's most established and respected private fertility providers, renowned for combining clinical excellence with compassionate, personalised care. The clinic supports NHS and self-funded patients from a wide range of backgrounds, including solo parents, couples, and LGBTQIA+ families.

With a strong reputation for innovation and inclusivity, the organisation is committed to delivering outstanding patient care while fostering a collaborative and supportive working environment for its clinical teams.

We are recruiting an experienced Nurse Manager to lead the nursing team within a busy, high-performing fertility clinic based in a prestigious clinic in North East England. This is an excellent opportunity for a confident clinical leader who is passionate about delivering outstanding patient care while supporting and developing a multidisciplinary nursing team.

The successful candidate will oversee the day-to-day management of the nursing department, ensuring the highest standards of clinical practice, patient experience, and operational efficiency.

The ideal candidate will be a proactive leader with strong fertility experience, excellent communication skills, commercial awareness, and the ability to inspire and motivate others in a fast-paced environment.

• Must be UK-based.
• Registered Nurse (NMC).
• Previous experience within fertility/IVF services.
• Qualified and experienced in ultrasound monitoring.
• Previous leadership or management experience within a clinical setting.
• Excellent communication and interpersonal skills.
• Strong commercial awareness and understanding of clinic performance.
• Strong organisational and time management abilities.
• Ability to lead, mentor and support a multidisciplinary nursing team.
• High attention to detail with excellent clinical governance awareness.
• Strong IT and administrative skills.
• Ability to work effectively in a busy, patient-focused environment.

• Independent Prescriber qualification (not essential but would be an advantage).

• Opportunity to join one of the UK's leading fertility providers.
• Supportive and collaborative clinical environment.
• Ongoing professional development and career progression opportunities.
• Competitive salary and benefits package.
• The opportunity to make a meaningful difference in the lives of patients and families every day.

If you are an experienced fertility nurse leader looking for your next career opportunity in a prestigious clinic in North East England, we would love to hear from you.

Fixed term contract. 6-9 months.

We are recruiting for a fertility diagnostics company developing PCR-based testing solutions. With a focus on precision and regulatory rigour, the business is building the validation infrastructure needed to bring its diagnostics platform to market under UK regulatory frameworks.

We are seeking a Validation Engineer on a fixed-term contract (6–9 months) to lead the writing and formalisation of the validation documentation suite. This is a primarily office-based, documentation-focused role: the scientific lead will run the experiments, and the successful candidate will translate those results into fully compliant validation protocols and reports.

The ideal candidate will have a strong grasp of PCR-based diagnostic workflows, ideally with experience in DDP, and a track record of producing validation documentation to ISO 15189, ISO 13485, MHRA (IVDD/IVDR), and UKAS standards. At the end of the contract, deliverables and knowledge will be handed over to the incoming Quality Manager.

1. Validation Protocol Writing
   Author comprehensive validation protocols and reports aligned to ISO 15189, ISO 13485, MHRA (IVDD/IVDR), and UKAS requirements.
   Work directly with the scientific lead to understand experimental design and translate results into formal documentation.
   Produce validation reports that may run to several hundred pages — accuracy and regulatory alignment are paramount.
2. Regulatory Compliance
   Ensure all validation documentation meets applicable MHRA (IVDD/IVDR) regulations.
   Maintain awareness of evolving UK IVD regulatory requirements and apply them to documentation deliverables.
   Support preparation for UKAS accreditation activities as required.
3. PCR Workflow Understanding
   Apply working knowledge of PCR-based diagnostic workflows to contextualise and validate experimental data.
   Engage with DDP (Droplet Digital PCR) workflows where relevant to the validation programme.
   Liaise with laboratory scientists to ensure technical accuracy of all written outputs.
4. Handover & Knowledge Transfer
   Structure validation documentation for long-term maintainability and ease of handover.
   Deliver a clean, complete handover package to the incoming Quality Manager at contract end.
   Document processes and decisions to support continuity of the quality function.

• Background in molecular biology or a closely related life science discipline.
• Hands‑on experience in a diagnostic laboratory environment.
• Proven track record writing validation protocols and reports for IVD products.
• Strong working knowledge of ISO 15189, ISO 13485, MHRA IVDD/IVDR, and UKAS standards.
• Experience with PCR-based diagnostic workflows; DDP experience is advantageous.
• Excellent written communication skills — this is primarily a documentation role.
• Ability to work independently and manage workload across a hybrid schedule.
• Available for a fixed-term engagement of 6–9 months.

We are recruiting for a fertility diagnostics company developing PCR-based testing solutions. With a focus on precision and regulatory rigour, the business is building the validation infrastructure needed to bring its diagnostics platform to market under UK regulatory frameworks.

We are seeking a Validation Engineer on a fixed-term contract (6–9 months) to lead the writing and formalisation of the validation documentation suite. This is a primarily office-based, documentation-focused role: the scientific lead will run the experiments, and the successful candidate will translate those results into fully compliant validation protocols and reports. The ideal candidate will have a strong grasp of PCR-based diagnostic workflows, ideally with experience in DDP, and a track record of producing validation documentation to ISO 15189, ISO 13485, MHRA (IVDD/IVDR), and UKAS standards.

At the end of the contract, deliverables and knowledge will be handed over to the incoming Quality Manager.

1. Validation Protocol Writing: Author comprehensive validation protocols and reports aligned to ISO 15189, ISO 13485, MHRA (IVDD/IVDR), and UKAS requirements. Work directly with the scientific lead to understand experimental design and translate results into formal documentation. Produce validation reports that may run to several hundred pages — accuracy and regulatory alignment are paramount.
2. Regulatory Compliance: Ensure all validation documentation meets applicable MHRA (IVDD/IVDR) regulations. Maintain awareness of evolving UK IVD regulatory requirements and apply them to documentation deliverables. Support preparation for UKAS accreditation activities as required.
3. PCR Workflow Understanding: Apply working knowledge of PCR-based diagnostic workflows to contextualise and validate experimental data. Engage with DDP (Droplet Digital PCR) workflows where relevant to the validation programme. Liaise with laboratory scientists to ensure technical accuracy of all written outputs.
4. Handover & Knowledge Transfer: Structure validation documentation for long-term maintainability and ease of handover. Deliver a clean, complete handover package to the incoming Quality Manager at contract end. Document processes and decisions to support continuity of the quality function.

• Background in molecular biology or a closely related life science discipline
• Hands-on experience in a diagnostic laboratory environment
• Proven track record writing validation protocols and reports for IVD products
• Strong working knowledge of ISO 15189, ISO 13485, MHRA IVDD/IVDR, and UKAS standards
• Experience with PCR-based diagnostic workflows; DDP experience is advantageous
• Excellent written communication skills — this is primarily a documentation role
• Ability to work independently and manage workload across a hybrid schedule
• Available for a fixed-term engagement of 6–9 months

Location: Coventry, United Kingdom

The Ivf Guide seeks a Validation Engineer for a fixed-term 6–9 month contract to lead the validation documentation suite for a PCR-based diagnostics platform. The role is primarily office-based and documentation-focused, with the scientific lead running experiments and the candidate translating results into compliant protocols and reports.

Ideal candidates have a molecular biology background and solid experience producing validation documentation to ISO 15189, ISO 13485, MHRA IVDD/IVDR, and UKAS

The Ivf Guide is seeking a Nurse Manager to lead our nursing team at a busy fertility clinic in London. You will drive clinical excellence, patient experience and operational efficiency while mentoring a multidisciplinary nursing team.

The ideal candidate will have extensive fertility nursing leadership experience, strong ultrasound monitoring skills, and excellent communication and governance mindset. UK-based with NMC registration is essential.

The IVF Guide in London is seeking an experienced Nurse Manager to lead the nursing team at a busy fertility clinic. You will drive clinical governance, patient care standards and operational efficiency.

You will mentor a multidisciplinary nursing group, partner with clinicians, and support service development in a fast-paced environment. UK-based RN with NMC registration and fertility/IVF experience is essential.

About the Client

Our client is one of the UK's most established and respected private fertility providers, renowned for combining clinical excellence with compassionate, personalised care. The clinic supports NHS and self-funded patients from a wide range of backgrounds, including solo parents, couples and LGBTQIA+ families.

With a strong reputation for innovation and inclusivity, the organisation is committed to delivering outstanding patient care while fostering a collaborative and supportive working environment for its clinical teams.

Nurse Manager (Fertility) – London, UK

Permanent | Full-time

We are recruiting an experienced Nurse Manager to lead the nursing team within a busy, high‑performing fertility clinic based in London. This is an excellent opportunity for a confident clinical leader who is passionate about delivering outstanding patient care while supporting and developing a multidisciplinary nursing team.

The successful candidate will oversee the day‑to‑day management of the nursing department, ensuring the highest standards of clinical practice, patient experience and operational efficiency. The ideal candidate will be a proactive leader with strong fertility experience, excellent communication skills, commercial awareness, and the ability to inspire and motivate others in a fast‑paced environment.

• UK based
• Registered Nurse (NMC)
• Previous experience within fertility/IVF services
• Qualified and experienced in ultrasound monitoring
• Leadership or management experience within a clinical setting
• Excellent communication and interpersonal skills
• Strong commercial awareness and understanding of clinic performance
• Strong organisational and time‑management skills
• Ability to lead, mentor and support a multidisciplinary nursing team
• High attention to detail with excellent clinical governance awareness
• Strong IT and administrative skills
• Ability to work effectively in a busy, patient‑focused environment

• Independent Prescriber qualification (not essential but would be an advantage)

• Opportunity to join one of the UK's leading fertility providers
• Supportive and collaborative clinical environment
• Ongoing professional development and career progression opportunities
• Competitive salary and benefits package The opportunity to make a meaningful difference in the lives of patients and families every day

If you are an experienced fertility nurse leader looking for your next career opportunity in London, we would love to hear from you.

The IVF Guide is seeking a Validation Engineer for a fixed-term contract (6–9 months) to lead the writing and formalisation of the validation documentation suite. This is a documentation-focused, office-based role: the scientific lead will run experiments, and you will translate results into fully compliant validation protocols and reports.

The ideal candidate will have strong PCR-based diagnostic experience, ideally with DDP, and a track record of producing validation documentation to ISO