Description The File Handler will manage a caseload of varied EL/PL cases on behalf of a number of insurance clients. The role requires a forensic and analytical approach to employer and public liability issues together with experience and/or appreciation of the documents and evidence required in these types of cases. The majority of the cases will be Fast-Track with the potential to handle Multi Track cases up to £100K, cases are generally handled on a non-delegated authority basis. Key Responsibilities Considering concepts and merits of primary and secondary liability in employer and public liability claims. Handling matters in accordance with client SLA's. Initial report/review and setting strategy for the management of the claim. Reviewing evidence (eg. Witness statements, GP records, Occupational Health/ Personnel records, property inspection reports). Dealing with Disclosure. Conducting investigations. Conducting CMC's and applications. Review and report re exchange of evidence, receipt of medical evidence, joints statements or at any other stage. Instructing Counsel/investigators/medical and other experts. Drafting questions to medical experts. Costs Schedules. Dealing with routine correspondence & reviewing matters throughout. Drafting in general. Research. Counter Schedule. Pre-Trial reports. Attending Conferences and Trial with Counsel. Preparing/checking Trial Bundles. CRU appeal. To ensure compliance with the SRA Standards & Regulations. Working Hours 35 hours per week Monday - Friday 9am - 5pm with 1 unpaid hour for lunch. Primary location for this role is Parklands, Bolton Office. We are hybrid workers with attendance required 1 day a week in the office Skills, Knowledge and Expertise Experience of handling a caseload of EL/PL files. Previous litigation experience. Meeting targets. Positive, confident and enthusiastic. Good advocacy skills. Excellent listening, verbal and written communication skills. Good client care skills and evidence of working to client guidelines on a non-delegated basis. Ability to prioritise work, keep to deadlines and work under pressure. High level of analytical skills. Ability to make decisions and delegate effectively. Ability to anticipate problems and identify solutions. Ability to maintain concentration and pay attention to detail. Driven to achieve. Excellent IT Skills. Ability to work within the Keoghs Shared Values framework. The ability to demonstrate resilience and self-control. Values Our culture is focussed on making Keoghs sustainable and successful for our people and clients, with this our five values are at the heart of everything we do; We are connectedWe are innovativeWe are dynamicWe succeed together Benefits Davies Incentive Plan 25 days holiday per year which increases with level of service (opportunity to buy & sell 3 days) Family Cover Private Medical Insurance (Bupa) - will automatically be at single cover level but can opt into family option within first month of joining. Simply Health Care Cash Plan WeCare - 24/7 online GP, mental health support and virtual wellbeing covering a whole host of topics to do with health, mental health, wellbeing & healthy living and financial & legal wellbeing Death in Service Critical Illness Cover PHI/Income Protection (Private health insurance) Pension Contribution based 5% Employee / 3% Employer Employee Resource Groups Employee Volunteering Programme Cycle to Work Scheme Tech Scheme Season Ticket Loan Gym Flex Access to Online Discount Sites Discounted Gourmet Society Membership Discounted Tickets for Merlin Attractions nationwide Discounts at local retail outlets after successfully completing probation
Apr 02, 2026
Full time
Description The File Handler will manage a caseload of varied EL/PL cases on behalf of a number of insurance clients. The role requires a forensic and analytical approach to employer and public liability issues together with experience and/or appreciation of the documents and evidence required in these types of cases. The majority of the cases will be Fast-Track with the potential to handle Multi Track cases up to £100K, cases are generally handled on a non-delegated authority basis. Key Responsibilities Considering concepts and merits of primary and secondary liability in employer and public liability claims. Handling matters in accordance with client SLA's. Initial report/review and setting strategy for the management of the claim. Reviewing evidence (eg. Witness statements, GP records, Occupational Health/ Personnel records, property inspection reports). Dealing with Disclosure. Conducting investigations. Conducting CMC's and applications. Review and report re exchange of evidence, receipt of medical evidence, joints statements or at any other stage. Instructing Counsel/investigators/medical and other experts. Drafting questions to medical experts. Costs Schedules. Dealing with routine correspondence & reviewing matters throughout. Drafting in general. Research. Counter Schedule. Pre-Trial reports. Attending Conferences and Trial with Counsel. Preparing/checking Trial Bundles. CRU appeal. To ensure compliance with the SRA Standards & Regulations. Working Hours 35 hours per week Monday - Friday 9am - 5pm with 1 unpaid hour for lunch. Primary location for this role is Parklands, Bolton Office. We are hybrid workers with attendance required 1 day a week in the office Skills, Knowledge and Expertise Experience of handling a caseload of EL/PL files. Previous litigation experience. Meeting targets. Positive, confident and enthusiastic. Good advocacy skills. Excellent listening, verbal and written communication skills. Good client care skills and evidence of working to client guidelines on a non-delegated basis. Ability to prioritise work, keep to deadlines and work under pressure. High level of analytical skills. Ability to make decisions and delegate effectively. Ability to anticipate problems and identify solutions. Ability to maintain concentration and pay attention to detail. Driven to achieve. Excellent IT Skills. Ability to work within the Keoghs Shared Values framework. The ability to demonstrate resilience and self-control. Values Our culture is focussed on making Keoghs sustainable and successful for our people and clients, with this our five values are at the heart of everything we do; We are connectedWe are innovativeWe are dynamicWe succeed together Benefits Davies Incentive Plan 25 days holiday per year which increases with level of service (opportunity to buy & sell 3 days) Family Cover Private Medical Insurance (Bupa) - will automatically be at single cover level but can opt into family option within first month of joining. Simply Health Care Cash Plan WeCare - 24/7 online GP, mental health support and virtual wellbeing covering a whole host of topics to do with health, mental health, wellbeing & healthy living and financial & legal wellbeing Death in Service Critical Illness Cover PHI/Income Protection (Private health insurance) Pension Contribution based 5% Employee / 3% Employer Employee Resource Groups Employee Volunteering Programme Cycle to Work Scheme Tech Scheme Season Ticket Loan Gym Flex Access to Online Discount Sites Discounted Gourmet Society Membership Discounted Tickets for Merlin Attractions nationwide Discounts at local retail outlets after successfully completing probation
We're looking for a Lab Analyst to join our Compliance team, supporting the delivery of high-quality analytical testing to ensure the safety, quality, and compliance of our products. You'll work hands on with laboratory equipment such as GC MS and HPLC, collaborate with teams across the business, and maintain accurate records in line with regulatory and ISO standards. This role suits someone with a science related degree (or equivalent), a strong attention to detail, and a proactive approach to learning new techniques while contributing to continuous improvement in a quality focused laboratory environment. Key Responsibilities Collaborate with the Compliance, Mixing, Production, and Projects teams to deliver daily on project goals. Demonstrate technical competence in the use of specified instruments and equipment; Gas Chromatography Mass Spectrometry (GC MS), High Performance Liquid Chromatography (HPLC), density, Specific Gravity (SG), Reflective Index (RI). Shimadzu equipment experience is advantageous. Produce high quality analysis and accurate test data implementing a robust understanding of TPD and TRPR. Prepare and perform standard testing procedures, including preparation of materials, and setting up and calibrating equipment. Completing testing with consistent diligence and excellent quality. Receive training and test raw materials, finished goods, end of life testing and any other testing required. Trusted to at all times comply with health and safety policies and procedures including COSHH, risk assessments, personal protective equipment (PPE) use, manual handling, and emergency procedures. Maintain excellent housekeeping, follow the organisation's Standard Operation Procedures (SOPs), and ensure the lab is clean and tidy at all times. Under the direction of the Head of Quality & Compliance and Compliance Manager, order and control stocks of laboratory materials where required. Demonstrate problem solving techniques including identification of sources of error and strive to innovate new methods of how sources of error can be reduced. Quality control/assurance (QC/QA) experience is beneficial. Identify, organise, and use resources effectively to complete tasks. Focus on QC release testing and investigatory analysis to guarantee the quality and safety of products. Adhere to internal and external regulatory requirements; following ISO 9001 (Quality) and ISO 14001 (Environmental) management systems standards. Report faults and seek diagnostic advice to maintain equipment in good working order, including calibration and servicing where required. Communicate confidently and keep accurate detailed records of laboratory work & results undertaken. Use Laboratory Information Management systems to support their work. Address non routine problems with samples and instrumentation, within defined areas. Participate in continuous performance improvement of systems and processes relevant to the work environment e.g. workplace organisation techniques, accreditation (e.g. ISO, UKAS) and proficiency testing. Evaluate data, recognise, and call attention to anomalous or unusual results. Able to generate reports. Ensure any retain/lab samples are properly organised. What we're looking for A science related degree or equivalent qualification in a relevant scientific discipline. Strong attention to detail and a commitment to producing accurate, high quality data. A proactive learner with an interest in developing new skills, techniques, and technologies. Good problem solving skills and the ability to manage non routine testing challenges. Confidence using laboratory software, LIMS, and Microsoft Office applications. A collaborative team player who works in line with our values of Trust, Excellence, Collaboration, Innovation, and Passion. What's on Offer Competitive salary commensurate with experience 30 days holiday increasing with service Life Insurance benefit Cashback healthcare plan (Westfield Health) Discounts on our products to assist with smoking cessation Cycle to Work Scheme Additional benefits with service (access to company caravan, enhanced family friendly policies) We look forward to reviewing your application and potentially welcoming you to our team. Flavour Warehouse is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences.
Apr 02, 2026
Full time
We're looking for a Lab Analyst to join our Compliance team, supporting the delivery of high-quality analytical testing to ensure the safety, quality, and compliance of our products. You'll work hands on with laboratory equipment such as GC MS and HPLC, collaborate with teams across the business, and maintain accurate records in line with regulatory and ISO standards. This role suits someone with a science related degree (or equivalent), a strong attention to detail, and a proactive approach to learning new techniques while contributing to continuous improvement in a quality focused laboratory environment. Key Responsibilities Collaborate with the Compliance, Mixing, Production, and Projects teams to deliver daily on project goals. Demonstrate technical competence in the use of specified instruments and equipment; Gas Chromatography Mass Spectrometry (GC MS), High Performance Liquid Chromatography (HPLC), density, Specific Gravity (SG), Reflective Index (RI). Shimadzu equipment experience is advantageous. Produce high quality analysis and accurate test data implementing a robust understanding of TPD and TRPR. Prepare and perform standard testing procedures, including preparation of materials, and setting up and calibrating equipment. Completing testing with consistent diligence and excellent quality. Receive training and test raw materials, finished goods, end of life testing and any other testing required. Trusted to at all times comply with health and safety policies and procedures including COSHH, risk assessments, personal protective equipment (PPE) use, manual handling, and emergency procedures. Maintain excellent housekeeping, follow the organisation's Standard Operation Procedures (SOPs), and ensure the lab is clean and tidy at all times. Under the direction of the Head of Quality & Compliance and Compliance Manager, order and control stocks of laboratory materials where required. Demonstrate problem solving techniques including identification of sources of error and strive to innovate new methods of how sources of error can be reduced. Quality control/assurance (QC/QA) experience is beneficial. Identify, organise, and use resources effectively to complete tasks. Focus on QC release testing and investigatory analysis to guarantee the quality and safety of products. Adhere to internal and external regulatory requirements; following ISO 9001 (Quality) and ISO 14001 (Environmental) management systems standards. Report faults and seek diagnostic advice to maintain equipment in good working order, including calibration and servicing where required. Communicate confidently and keep accurate detailed records of laboratory work & results undertaken. Use Laboratory Information Management systems to support their work. Address non routine problems with samples and instrumentation, within defined areas. Participate in continuous performance improvement of systems and processes relevant to the work environment e.g. workplace organisation techniques, accreditation (e.g. ISO, UKAS) and proficiency testing. Evaluate data, recognise, and call attention to anomalous or unusual results. Able to generate reports. Ensure any retain/lab samples are properly organised. What we're looking for A science related degree or equivalent qualification in a relevant scientific discipline. Strong attention to detail and a commitment to producing accurate, high quality data. A proactive learner with an interest in developing new skills, techniques, and technologies. Good problem solving skills and the ability to manage non routine testing challenges. Confidence using laboratory software, LIMS, and Microsoft Office applications. A collaborative team player who works in line with our values of Trust, Excellence, Collaboration, Innovation, and Passion. What's on Offer Competitive salary commensurate with experience 30 days holiday increasing with service Life Insurance benefit Cashback healthcare plan (Westfield Health) Discounts on our products to assist with smoking cessation Cycle to Work Scheme Additional benefits with service (access to company caravan, enhanced family friendly policies) We look forward to reviewing your application and potentially welcoming you to our team. Flavour Warehouse is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences.
Job Purpose The Associate Director Clinical Operations is responsible for the management of all aspects of the Clinical Study Team activities for assigned clinical studies. In concert with the Director Clinical Operations, is accountable for achieving successful execution and delivery of MoonLake's clinical development team activities at the study level by meeting company and regulatory requirements according to time, quality/scope and budget constraints. Key Accountabilities: Lead the clinical study team tasked with the delivery of MoonLake sponsored studies. Assist in the selection of appropriate vendors for the conduct of MoonLake sponsored studies. Ensure a detailed project plan is in place for the studies and work with the CRO and MoonLake team to set priorities and manage timelines. Responsible for oversight of assigned clinical studies ensuring they are conducted in compliance with the protocol, study plans, relevant guidelines and contracts through regular vendor and/or investigator site contact. Perform accompanied site/vendor visits as part of Sponsor oversight. Monitor the quality of vendor deliverables, address quality issues with the appropriate team member and escalate to the Director Clinical Operations, when appropriate. Monitor the status of clinical data collection of assigned clinical studies. Develop/review study management plans ensuring Sponsor oversight of clinical studies in accordance with MoonLake procedures. Review vendor generated clinical study related documents to ensure compliance with the objectives of the study, MoonLake procedures and relevant standards. Act as the key contact for study associated vendors and ensure timely and effective communication between involved parties. Review and approve vendor responses to quality assurance audits for appropriateness, timeliness and accordance with company SOPs and regulatory requirements. Ensure essential documents allowing the reconstruction of each study are generated, filed and maintained by or on behalf of MoonLake. Communicate progress and identify risks and issues arising on the assigned clinical studies to the Director Clinical Operations and other MoonLake development project team members as appropriate. Ensure compliance with MoonLake procedures and SOPs. Help train/mentor more junior clinical operations team members, as required. Participate in the preparation, review, updating and training of SOPs and may serve as clinical operations representative for internal process/system development. Your profile Education: Bachelor's degree in Life Sciences, Nursing or other health care professional equivalent. Experience: Minimum of 8 years of clinical operations experience, with increasing levels of responsibility. 5+ years of clinical project management experience at a sponsor or CRO company. Substantial experience of managing outsourced global clinical studies. Therapeutic experience in dermatology and rheumatology or relevant indications, ideally experience of biological therapies. Skills/knowledge/behavioural competencies: Excellent communication skills and able to effectively convey messages across to both internal and external study team members. Highly organised, able to prioritise work, work well under pressure and meet deadlines. Independent, self-starter with a proactive, problem-solving approach. Ability to work with little or no supervision. High attention to detail always. Must have a 'one of a kind' work ethic and must exhibit a great level of self-discipline. Work Location 2 days a week in our brand new Cambridge or Porto office. Some travel may be required. Why us? An exciting job opportunity awaits you! MoonLake is a dynamic and innovative company pushing the boundaries of possibility, and we are looking for passionate individuals to join our stellar team. What we offer: Learning Environment: An opportunity to learn and grow alongside experienced professionals in a supportive and innovative biotech environment. Impactful Work: Contribute to ground-breaking projects that have the potential to transform global healthcare. Flexibility and Balance: Work remotely/hybrid, enjoying a healthy work-life balance while making meaningful contributions to our team. Career Growth: A clear path for career progression, with the chance to take on more responsibilities as you develop your skills. Our Core Values We do Stellar Science: We aspire to create novel therapies that elevate treatment horizons, with innovative science, and high quality, always. We go beyond: We aspire to be positively disruptive in our field, and bold in the way we challenge the norms and each other. We unlock value: We aspire to create long-term value for investors and communities.
Apr 02, 2026
Full time
Job Purpose The Associate Director Clinical Operations is responsible for the management of all aspects of the Clinical Study Team activities for assigned clinical studies. In concert with the Director Clinical Operations, is accountable for achieving successful execution and delivery of MoonLake's clinical development team activities at the study level by meeting company and regulatory requirements according to time, quality/scope and budget constraints. Key Accountabilities: Lead the clinical study team tasked with the delivery of MoonLake sponsored studies. Assist in the selection of appropriate vendors for the conduct of MoonLake sponsored studies. Ensure a detailed project plan is in place for the studies and work with the CRO and MoonLake team to set priorities and manage timelines. Responsible for oversight of assigned clinical studies ensuring they are conducted in compliance with the protocol, study plans, relevant guidelines and contracts through regular vendor and/or investigator site contact. Perform accompanied site/vendor visits as part of Sponsor oversight. Monitor the quality of vendor deliverables, address quality issues with the appropriate team member and escalate to the Director Clinical Operations, when appropriate. Monitor the status of clinical data collection of assigned clinical studies. Develop/review study management plans ensuring Sponsor oversight of clinical studies in accordance with MoonLake procedures. Review vendor generated clinical study related documents to ensure compliance with the objectives of the study, MoonLake procedures and relevant standards. Act as the key contact for study associated vendors and ensure timely and effective communication between involved parties. Review and approve vendor responses to quality assurance audits for appropriateness, timeliness and accordance with company SOPs and regulatory requirements. Ensure essential documents allowing the reconstruction of each study are generated, filed and maintained by or on behalf of MoonLake. Communicate progress and identify risks and issues arising on the assigned clinical studies to the Director Clinical Operations and other MoonLake development project team members as appropriate. Ensure compliance with MoonLake procedures and SOPs. Help train/mentor more junior clinical operations team members, as required. Participate in the preparation, review, updating and training of SOPs and may serve as clinical operations representative for internal process/system development. Your profile Education: Bachelor's degree in Life Sciences, Nursing or other health care professional equivalent. Experience: Minimum of 8 years of clinical operations experience, with increasing levels of responsibility. 5+ years of clinical project management experience at a sponsor or CRO company. Substantial experience of managing outsourced global clinical studies. Therapeutic experience in dermatology and rheumatology or relevant indications, ideally experience of biological therapies. Skills/knowledge/behavioural competencies: Excellent communication skills and able to effectively convey messages across to both internal and external study team members. Highly organised, able to prioritise work, work well under pressure and meet deadlines. Independent, self-starter with a proactive, problem-solving approach. Ability to work with little or no supervision. High attention to detail always. Must have a 'one of a kind' work ethic and must exhibit a great level of self-discipline. Work Location 2 days a week in our brand new Cambridge or Porto office. Some travel may be required. Why us? An exciting job opportunity awaits you! MoonLake is a dynamic and innovative company pushing the boundaries of possibility, and we are looking for passionate individuals to join our stellar team. What we offer: Learning Environment: An opportunity to learn and grow alongside experienced professionals in a supportive and innovative biotech environment. Impactful Work: Contribute to ground-breaking projects that have the potential to transform global healthcare. Flexibility and Balance: Work remotely/hybrid, enjoying a healthy work-life balance while making meaningful contributions to our team. Career Growth: A clear path for career progression, with the chance to take on more responsibilities as you develop your skills. Our Core Values We do Stellar Science: We aspire to create novel therapies that elevate treatment horizons, with innovative science, and high quality, always. We go beyond: We aspire to be positively disruptive in our field, and bold in the way we challenge the norms and each other. We unlock value: We aspire to create long-term value for investors and communities.
Your new company A leading national legal services provider is seeking an experienced Personal Injury Lawyer to manage a varied caseload of litigated and non-litigated personal injury files valued up to £100,000. You will take full ownership of each claim from instruction through to settlement or litigation, ensuring excellent client care, proactive case progression and strong technical decision-making. This is an exciting opportunity to join a large, well-established organisation known for delivering high-quality legal and insurance services. You'll benefit from a supportive, collaborative environment with significant opportunities for development. Your new role As a Personal Injury Solicitor/CILEX, your responsibilities will include: Manage a caseload of litigated and non-litigated PI claims up to £100,000, ensuring files are progressed efficiently, proactively and profitably. Deliver exceptional client service, maintaining regular communication and providing clear, concise advice. Handle a wide range of RTA Portal and Fixed Fee cases, including MIB (uninsured and untraced) matters. Obtain medical and non-medical evidence in line with track requirements and recoverability. Issue proceedings via the Court Portal and attend conferences, hearings and CMCs where required. Advise clients on litigation risk, costs exposure and issues relating to fundamental dishonesty. Maintain compliance with the CPR, professional conduct rules and internal policies. Build effective working relationships with defendant solicitors, insurers and external stakeholders. Negotiate liability and quantum where possible. Support junior team members through mentoring where appropriate. May be appointed as an authorised person when required. What you'll need to Qualified Solicitor or CILEx Lawyer (or working towards qualification/litigation rights). Proven experience managing your own PI caseload (litigated & non-litigated), including RTA Portal and Intermediate Track matters. EL/PL or OL experience is advantageous but not essential. Experience working to fee or settlement targets. Strong knowledge of the CPR, relevant case law and PI legislation. Excellent written and verbal communication skills with a focus on client care. Ability to work collaboratively with external agencies, including medical experts, investigators and counsel. Strong IT proficiency, What you'll get in return Competitive salary of up to £45,000 Hybrid working of 3 days WFH per week Clear progression opportunities Opportunity to get involved in a wide mix of claimant personal injury work valued up to £100,000 What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. Alternatively, email or call us now on .If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk
Apr 01, 2026
Full time
Your new company A leading national legal services provider is seeking an experienced Personal Injury Lawyer to manage a varied caseload of litigated and non-litigated personal injury files valued up to £100,000. You will take full ownership of each claim from instruction through to settlement or litigation, ensuring excellent client care, proactive case progression and strong technical decision-making. This is an exciting opportunity to join a large, well-established organisation known for delivering high-quality legal and insurance services. You'll benefit from a supportive, collaborative environment with significant opportunities for development. Your new role As a Personal Injury Solicitor/CILEX, your responsibilities will include: Manage a caseload of litigated and non-litigated PI claims up to £100,000, ensuring files are progressed efficiently, proactively and profitably. Deliver exceptional client service, maintaining regular communication and providing clear, concise advice. Handle a wide range of RTA Portal and Fixed Fee cases, including MIB (uninsured and untraced) matters. Obtain medical and non-medical evidence in line with track requirements and recoverability. Issue proceedings via the Court Portal and attend conferences, hearings and CMCs where required. Advise clients on litigation risk, costs exposure and issues relating to fundamental dishonesty. Maintain compliance with the CPR, professional conduct rules and internal policies. Build effective working relationships with defendant solicitors, insurers and external stakeholders. Negotiate liability and quantum where possible. Support junior team members through mentoring where appropriate. May be appointed as an authorised person when required. What you'll need to Qualified Solicitor or CILEx Lawyer (or working towards qualification/litigation rights). Proven experience managing your own PI caseload (litigated & non-litigated), including RTA Portal and Intermediate Track matters. EL/PL or OL experience is advantageous but not essential. Experience working to fee or settlement targets. Strong knowledge of the CPR, relevant case law and PI legislation. Excellent written and verbal communication skills with a focus on client care. Ability to work collaboratively with external agencies, including medical experts, investigators and counsel. Strong IT proficiency, What you'll get in return Competitive salary of up to £45,000 Hybrid working of 3 days WFH per week Clear progression opportunities Opportunity to get involved in a wide mix of claimant personal injury work valued up to £100,000 What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. Alternatively, email or call us now on .If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk
New opportunity to join one of the UK's leading independent bulk liquid storage providers, operating four strategically located terminals across the country. The Company supports a wide range of sectors including chemicals, petroleum, gases, bitumen, and emerging energy markets such as hydrogen, sustainable aviation fuel (SAF) and carbon capture. As a key part of the UK's critical national infrastructure, Navigator is committed to safe operations, exceptional customer service, and ongoing investment to support future growth and the energy transition. A vacancy now exists for an HSE Manager to join the team. Negotiable Salary + Bonus + Private Healthcare The role: Act as the competent person / principal health, safety and environmental advisor for the Thames Terminal. Identify areas of potential improvement within the HSE function and present these findings to senior managers for approval. Once approved scope, implement and embed ideas and methodology Ensure that the Terminal discharges its obligations under health, safety and environmental legislation, corporate standards and the UK Health, Safety and Environmental policy. Provide an effective Terminal occupational health, safety, welfare and environmental function by developing and implementing initiatives, structures, strategies, policies and procedures. Advise and guide the Terminal Management Team in the strategic management of health, safety, welfare and environmental issues ensuring they are aware of their obligations and are briefed on key issues that may affect the terminal. Monitor process safety performance and advise the terminal and senior management teams on requirements with regard to the prevention of major accidents and the safe movement of hazardous products. Prepare, monitor and review company policies, codes, practice and procedures including the safety management system relating to Health, Safety and Environmental matters in consultation with the UK Head of SHEQ, terminal management teams, departmental managers and other employees. Co-operate with technical and other staff in the management of contractors including: the production of Permits to Work; Method Statements; Risk Assessments and aiding in identifying hazards and required controls. Participate in Safety Audits, Permit Audits and Safety Observation Rounds. Manage and facilitate Terminal Safety meetings. Assist the terminal to ensure employees, contractors and visitors adhere to the UK Policy on site security. Ensure that all incidents and near misses are recorded on the company's reporting database and, where required, assist the terminal to ensure that they are properly investigated and analysed. Develop a working relationship with other other sites to ensure an open environment in which to share safety learnings. Identify and prioritise health, safety and environmental training needs, schemes and initiatives within the terminal, arranging for, or delivering such training as appropriate. Contribute to the professional development of any SHE direct reports. Attend site out of hours as and when required. Act as the competent person to ensure that documentation relating to waste leaving the site is suitable to ensure legal compliance. Build and maintain professional knowledge and disseminate this knowledge to managers and other professionals within the organisation, in line with business needs. This will assist in the development of best practises and contribute to the business performance and legal compliance. Any other task that may arise in the day-to-day functionality of this position Qualifications & Experience : Required: Relevant Health and Safety Qualification (IOSH, NEBOSH etc) Active involvement in the IOSH CPD programme Environmental Management qualification (PIEMA) Accident Investigator qualification (e.g. Tripod) 5 years' experience in the chemical or associated industry 2 years' experience in a safety and environmental related role Strong computer literacy including confidence in using Microsoft Office applications and the ability to learn new systems quickly.
Mar 13, 2026
Full time
New opportunity to join one of the UK's leading independent bulk liquid storage providers, operating four strategically located terminals across the country. The Company supports a wide range of sectors including chemicals, petroleum, gases, bitumen, and emerging energy markets such as hydrogen, sustainable aviation fuel (SAF) and carbon capture. As a key part of the UK's critical national infrastructure, Navigator is committed to safe operations, exceptional customer service, and ongoing investment to support future growth and the energy transition. A vacancy now exists for an HSE Manager to join the team. Negotiable Salary + Bonus + Private Healthcare The role: Act as the competent person / principal health, safety and environmental advisor for the Thames Terminal. Identify areas of potential improvement within the HSE function and present these findings to senior managers for approval. Once approved scope, implement and embed ideas and methodology Ensure that the Terminal discharges its obligations under health, safety and environmental legislation, corporate standards and the UK Health, Safety and Environmental policy. Provide an effective Terminal occupational health, safety, welfare and environmental function by developing and implementing initiatives, structures, strategies, policies and procedures. Advise and guide the Terminal Management Team in the strategic management of health, safety, welfare and environmental issues ensuring they are aware of their obligations and are briefed on key issues that may affect the terminal. Monitor process safety performance and advise the terminal and senior management teams on requirements with regard to the prevention of major accidents and the safe movement of hazardous products. Prepare, monitor and review company policies, codes, practice and procedures including the safety management system relating to Health, Safety and Environmental matters in consultation with the UK Head of SHEQ, terminal management teams, departmental managers and other employees. Co-operate with technical and other staff in the management of contractors including: the production of Permits to Work; Method Statements; Risk Assessments and aiding in identifying hazards and required controls. Participate in Safety Audits, Permit Audits and Safety Observation Rounds. Manage and facilitate Terminal Safety meetings. Assist the terminal to ensure employees, contractors and visitors adhere to the UK Policy on site security. Ensure that all incidents and near misses are recorded on the company's reporting database and, where required, assist the terminal to ensure that they are properly investigated and analysed. Develop a working relationship with other other sites to ensure an open environment in which to share safety learnings. Identify and prioritise health, safety and environmental training needs, schemes and initiatives within the terminal, arranging for, or delivering such training as appropriate. Contribute to the professional development of any SHE direct reports. Attend site out of hours as and when required. Act as the competent person to ensure that documentation relating to waste leaving the site is suitable to ensure legal compliance. Build and maintain professional knowledge and disseminate this knowledge to managers and other professionals within the organisation, in line with business needs. This will assist in the development of best practises and contribute to the business performance and legal compliance. Any other task that may arise in the day-to-day functionality of this position Qualifications & Experience : Required: Relevant Health and Safety Qualification (IOSH, NEBOSH etc) Active involvement in the IOSH CPD programme Environmental Management qualification (PIEMA) Accident Investigator qualification (e.g. Tripod) 5 years' experience in the chemical or associated industry 2 years' experience in a safety and environmental related role Strong computer literacy including confidence in using Microsoft Office applications and the ability to learn new systems quickly.
