Role Description The Nuclear Quality Assurance (QA) Manager is responsible for establishing, implementing, and maintaining a compliant Nuclear Quality Assurance Program in accordance with ASME NQA‑1, 10 CFR 50 Appendix B, 10 CFR Part 21, and applicable NRC and customer requirements. This role provides independent QA oversight across nuclear projects, suppliers, and internal execution teams, ensuring that safety‑related work is planned, performed, documented, and verified in full regulatory compliance, including ownership of the Nuclear QA Manual and implementing procedures. A key responsibility of this role is to reestablish and maintain a fully compliant ASME NQA‑1 Nuclear Quality Assurance Program, including restoration of governance, procedures, training, audit capability, and regulatory readiness. The position supports owner’s engineer, new build, advanced reactor/SMR, fuel cycle, life‑extension, and decommissioning projects and interfaces directly with clients, regulators, suppliers, and senior project leadership. Key Responsibilities - Nuclear Quality Assurance Program Leadership - Re-establish, implement, and maintain the Nuclear Quality Assurance Program in full compliance with ASME NQA‑1 and applicable NRC regulations - Maintain nuclear QA governance, procedures, training, audit programs, and records management - Establish a graded, risk-informed application of ASME NQA-1 appropriate to projects when full ASME NQA-1 program is not required - Define and enforce nuclear records lifecycle controls (creation, review/approval, retention, retrieval) to ensure traceability and audit readiness Company Description Worley is a global company of energy, chemicals and resources experts headquartered in Australia. We partner with our customers to deliver projects and create value across the life of their assets. We specialize in consulting, engineering, procurement and construction across the project lifecycle, with services extending through to operations and decommissioning. Leveraging extensive experience and AI-enabled delivery, we support customers in navigating complexity as they meet today's needs and transition to more sustainable solutions.

• Lead the sales activity in the assigned territory • Pursue target customers and maintain existing customer base • Develop market maps and successfully close orders to grow the overall territory • Meet or exceed territory order commitments and sales revenue forecast • Interact with customers in person and remotely to evaluate pumping solutions • Grow and develop targeted growth products and customers • Maintain organized and efficient lead and quote follow-up, expenses, planning, and reporting.

• Works collaboratively with internal and external teams (e.g., CROs, medical communications vendors, and external research partners) to coordinate the planning and execution of statistical deliverables related to clinical trials and RWE initiatives. • Plans, specifies, and performs statistical analyses for publications, including manuscripts, posters, and oral presentations. • Supports clinical trials as a study statistician, providing high-quality statistical support. • Contributes to interventional, observational, post-marketing, and RWE study design, and protocol development, including authoring the Statistics section in protocols and working cross-functionally on overall study design. • Authors SAPs for clinical trials, and develops shells for tables, figures, and listings. • Reviews CRF designs to ensure data collection supports the statistical analyses for primary, secondary, and exploratory endpoints. • Performs QC/QA of statistical deliverables, including validation of key analysis results. • Contributes to CSRs, including authoring statistical methods and interpreting study results. • Supports statistical activities for IND/NDA/MAA and other regulatory submissions and helps address statistical questions from FDA and other regulatory agencies. • Contributes to standardization and process improvement efforts for Biostatistics and to cross-functional process improvement. • Evaluates and, where appropriate, integrates AI tools to enhance the efficiency and quality of statistical activities.

Title: Bid Manager Location: Remote, United Kingdom Department: Business Development Job Title: Bid Manager Location: Home Based with requirement to attend regular business meetings at our offices (Manchester, Croydon or Tewkesbury) Salary: up to £50,000 per annum Status: Permanent Working Hours: Full Time Mon to Fri- 37.5 hours per week HCML is the UK’s leading provider of rehabilitation, case management, occupational health, and workplace wellbeing services. We’re proud to be recognised as a 2025 UK’s Best Workplace for Wellbeing, reflecting our commitment to supporting the growth, development, and wellbeing of our people. We are seeking an experienced and driven Bid Manager to join our Commercial team. The successful candidate will combine strong bid writing expertise with excellent project management skills, ensuring submissions are compelling, compliant and delivered at pace. Purpose of Role: This role will take ownership of the end-to-end bid lifecycle, leading the development, coordination and submission of high-quality tenders. This role operates within a highly collaborative environment and will work closely with colleagues across clinical, operational and commercial teams to deliver successful outcomes. Key Responsibilities: Bid Management & Delivery - Lead and manage the full bid lifecycle from opportunity qualification through to submission and post-submission activity. - Develop and manage bid plans, ensuring clear timelines, responsibilities and governance. - Drive bid progress, ensuring all inputs are delivered on time and to a high standard. Content Development & Writing - Write, edit and refine high-quality, persuasive tender responses. - Translate complex healthcare service delivery models into clear, engaging content. - Ensure a consistent, compelling narrative aligned to client requirements and evaluation criteria. Collaboration & Cross-Functional Working - Work as part of a collaborative Commercial function, supporting colleagues across multiple bids and opportunities. - Coordinate input from clinical, operational, finance and wider subject matter experts. - Contribute to cross-functional bids across HCML, providing both writing and bid management support where required. Compliance & Quality Assurance - Ensure all bids are fully compliant with tender documentation and submission requirements. - Maintain rigorous quality standards, including proofreading, formatting and version control. - Manage bid documentation and ensure submission readiness at all stages. Submission & Coordination - Lead submission of PQQs, ITTs, RFPs and framework applications. - Manage clarification questions and responses during the tender process. - Ensure all supporting documentation is accurate, complete and submitted on time. Continuous Improvement - Contribute to bid library development, capturing reusable content and best practice. - Support lessons learned and feedback reviews to continuously improve bid quality and win rates. Key Objectives - Deliver high-quality, compliant and competitive bids within agreed timelines. - Support improved conversion rates through clear, compelling submissions. - Enhance collaboration and consistency across HCML’s bid activity. Person Specification: Experience Essential - Minimum of 3 years in similar Bid Writer/Management Role - Proven experience managing bids end-to-end, from initiation through to submission. - Strong bid writing experience with a track record of successful submissions. - Experience coordinating multi-disciplinary teams in a fast-paced bid environment. Desirable - Experience within the Healthcare, Health, Insurance or Legal sectors Skills - Excellent written and verbal communication skills. - Strong organisational and project management capability - Ability to work under pressure and manage multiple deadlines effectively. - High attention to detail with strong proofreading and editing skills. - Confident stakeholder engagement and collaboration skills. Key Attributes - Collaborative and team-oriented, with a proactive approach to supporting colleagues. - Resilient and comfortable working in a deadline-driven environment. - Solutions-focused with a commitment to high-quality delivery. - Aligned to HCML’s values of quality, partnership and continuous improvement. Qualifications Essential - Degree level qualification or equivalent Desirable - Project management qualification Company Benefits: - Medicash Health Cash Plan: Which includes ability to claim back dental, optical, and chiropody costs. Plus, add your dependent children for free! + 24/7 Digital Health: Round-the-clock access to a virtual GP helpline and an Employee Assistance Programme (EAP) + Mental Health Support: Up to 8 fully funded face-to-face counselling or CBT sessions - Pension Scheme & Pension Salary Sacrifice - Peace of Mind: Rest easy knowing your loved ones are protected with a Death in Service benefit equal to 4x your base salary - Payroll Giving: Support the causes you love directly from your gross pay - Annual Leave: 25 days, plus Birthday Leave to celebrate your special day - Flexibility: Option to buy or sell up to 3 days of holiday each year - Giving Back: Up to 2 fully paid Volunteering/Community days per year - Family First: Enhanced, generous Maternity and Paternity policies, alongside comprehensive Company Sick Pay - Professional Development: We fund professional subscriptions and registrations (including CMS UK and HCPC) post-probation, alongside internal promotion and secondment opportunities - Rewarding Excellence: Annual pay reviews, discretionary bonus schemes, and regular staff awards to celebrate your hard work plus a regular events and activities throughout the year