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Job ID 2025-16109 Date posted 03/11/2025 Location Cambridge, United Kingdom Category Technical Writer Job Overview Are you passionate about writing and excited by ground-breaking technology? We are looking for highly motivated people to join Arm and help craft the next generation of Arm technologies! Our work influences 95% of the world’s connected devices running on Arm, across a variety of industries: from healthcare to smart homes. We’re looking for an expert technical author to lead content projects, mentor teammates, and shape the documentation for Arm's innovative Graphics, Image Signal, and Machine Learning processors. You will work closely with engineering teams and build the user documentation and content that Arm's partners need to make the best use of our products. Responsibilities • Lead and mentor a small team of Information Developers., • Plan, build, edit, and maintain user-centric content., • Advocate for high-quality content that is aligned with user needs and optimized for a global audience., • Collaborate with the team and the wider Arm community to improve what we do and how we work. Required Skills And Experience • 5+ years of hands-on experience in writing and people management., • Inclusive and collaborative leadership style., • Ability to independently lead complex documentation projects and release cycles., • Creative problem solver, flexible, and pragmatic in approach., • Clear communicator across multi-disciplinary teams., • Eager to learn about new technologies and evolving documentation practices. Nice To Haves These skills and experiences are not required for your application, but you will need a strong curiosity about acquiring them, and a passion for continuous improvement. We are keen to welcome innovative people into Arm! • Experience of working in the semiconductor industry., • Solid understanding of hardware design concepts such as RTL/IP integration, chip bring-up, validation, FPGA prototyping, and so on., • Familiarity with modern documentation workflows and tools such as reuse, single-sourcing, DITA, Markdown, and Git., • A good degree or postgraduate qualification in a relevant field, such as Computer Science, Physics, Maths, English, Linguistics, or Law. In Return Arm's culture offers a vibrant and encouraging community that empowers you to achieve and innovate. The opportunities to learn are endless, and we encourage you to take advantage of the many opportunities to do so, with time and resources dedicated to your professional development. Our attractive reward package is complemented by health and wellness benefits. Our 10x Mindset Guides How We Engineer, Collaborate, And Grow. Understand What It Means And How To Reflect 10x In Your Work Accommodations at Arm At Arm, we want to build extraordinary teams. If you need an adjustment or an accommodation during the recruitment process, please email Hybrid Working at Arm Arm’s approach to hybrid working is designed to create a working environment that supports both high performance and personal wellbeing. We believe in bringing people together face to face to enable us to work at pace, whilst recognizing the value of flexibility. Within that framework, we empower groups/teams to determine their own hybrid working patterns, depending on the work and the team’s needs. Details of what this means for each role will be shared upon application. In some cases, the flexibility we can offer is limited by local legal, regulatory, tax, or other considerations, and where this is the case, we will collaborate with you to find the best solution. Please talk to us to find out more about what this could look like for you. Equal Opportunities at Arm Arm is an equal opportunity employer, committed to providing an environment of mutual respect where equal opportunities are available to all applicants and colleagues. We are a diverse organization of dedicated and innovative individuals, and don’t discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

If you are a current Jazz employee please apply via the Internal Career site. \n Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to \ntransform the lives of patients and their families. We are dedicated to developing \nlife-changing medicines for people with serious diseases — often with limited or no \ntherapeutic options. We have a diverse portfolio of marketed medicines, including leading \ntherapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. \nOur patient-focused and science-driven approach powers pioneering research and development \nadvancements across our robust pipeline of innovative therapeutics in oncology and \nneuroscience. Jazz is headquartered in Dublin, Ireland with research and development \nlaboratories, manufacturing facilities and employees in multiple countries committed to \nserving patients worldwide. Please visit\n more information. \n Brief Description: The Associate Director, Medical Writing, is responsible for the efficient preparation of high-quality, strategically aligned medical writing deliverables within one or more program. S/he will work directly with cross functional teams to author regulatory documents (eg, protocols, clinical study reports, briefing books, submission documents, investigator brochures). For programs with multiple deliverables, s/he may be responsible for managing writers. The incumbent will ensure that strategically aligned communication points are conveyed in medical writing deliverables and that the communication points are consistent across program documentation. S/He will mitigate risk associated with medical writing and disclosure processes by contributing to Best Practices and SOPs. This role has global responsibilities, including participation in global teams and interaction with regulatory agencies in multiple regions. This role may have line management responsibilities. Essential Functions/Responsibilities * Works with the cross functional team to ensure effective communication of data in the respective documents. * Works with the cross functional team to ensure that communication needs for the clinical data are considered early in the development program to enable consistency of data presentation and messaging throughout the clinical program lifecycle. * Analyzes study level documents for their ability to deliver the information required by the target audience (eg, health authorities). * Communicates proactively and efficiently within the MW team and across R&D. * Ensures quality of medical writing deliverables and that work on assigned projects adheres to departmental procedures / practices, and industry / international standards. * Possible oversight of contract medical writers to ensure efficient preparation of medical writing deliverables for assigned clinical program(s) according to budget and timelines. * Collaboration and strategic partnership with cross functional team members to ensure understanding of program strategy and the nature of medical writing services required to deliver on company objectives. Required Knowledge, Skills, and Abilities * Exceptional English language skills and ability to write and edit complex material to ensure accuracy, clarity, and effectiveness. * Clear understanding of lean authoring for clinical regulatory documents. * A solid understanding of the clinical development process, including the documents that are required at each stage. * For early development: knowledge of pre-clinical and nonclinical regulatory requirements and reporting is required. * Prior contribution to, and an understanding of, global submissions. * Expert MS Office skills with a special focus on word processing, tables, spreadsheets, presentations, graphics and templates. * Excellent written and oral communication skills and demonstrated coaching and problem-solving abilities. * Knowledge of ICH and CTD guidelines for clinical and regulatory submission documents * Ability to think strategically; demonstrated negotiating skills and resourcefulness. * Demonstrated ability to manage several projects simultaneously. * Ability to critically analyze and synthesize complex scientific information. * High degree of influencing skills in shaping and developing content and wording. * Demonstrated ability to work collaboratively; multicultural sensitivity, builds positive and productive relationships, seeks input and demonstrates an appreciation for diverse views by incorporating them into decisions / proposals. * Successful track record of leading complex clinical / regulatory writing projects. * Demonstrated ability to make decisions even in the absence of complete information. * An excellent understanding of all aspect of ICH-GCP; keen insight on external clinical publication practices and standards (ICMJE, AMA, GPP). * Excellent organizational and time management skills and attention to detail. Required/Preferred Education and Licenses * BA/BS with at least 8 years (or advanced degree with at least 5 years) writing experience in the pharmaceutical industry across therapeutic areas required. Advanced degree preferred. #LI-DM1 Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $154,400.00 - $231,600.00 Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .

A growing organisation in the healthcare sector is seeking a Quality & Compliance Coordinator to support day-to-day Quality & Regulatory Affairs activities. Quality & Compliance Coordinator. This role is ideal for someone early in their career who brings strong organisation, attention to detail, and

Regulatory Solicitor, 4+ Years’ PQE, Cambridge, Up To C£90,000 (DOE) – Opportunity to join the expanding Regulatory team within an award winning, National law firm. You will have at least 4 years’ PQE in regulatory law within a national, regional or international law firm. JOB TIT

Azenta UK Ltd. Vice President & General Manager Consumable and Instruments Job Summary: The Vice President & General Manager (VP/GM) will lead and manage a key business unit within Azenta driving strategic growth operational excellence and financial performance. This position will be responsible for setting the vision developing and executing business strategies and ensuring alignment with Azentas overall strategic business objectives. The VP/GM will oversee all aspects of the business unit including P&L management product management and development customer engagement and team leadership. Key Responsibilities: Customer Relationship Ownership: Build and maintain strong relationships with key customers and strategic partners. Serve as the executive sponsor for major accounts ensuring alignment between customer needs and Azentas delivery capabilities. Ensure Azenta meets or exceeds expectations related to product performance service quality and innovation. Qualifications: • Bachelors degree in Business Life Sciences Engineering or related field; MBA or advanced degree preferred., • 15 years of progressive leadership experience in general management product management operations or P&L ownership., • Proven track record of leading a business unit or large organization within a life sciences biotech or technology-driven organization., • Experience managing complex operations and driving transformational growth., • Strong understanding of global markets and customer dynamics. Skills and Competencies: • Strategic thinker with strong business acumen and analytical skills., • Exceptional leadership and team-building capabilities., • Results-oriented with a focus on execution and operational excellence., • Excellent communication and interpersonal skills with the ability to influence at all levels., • High integrity resilience and adaptability in a fast-paced environment. Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race color age religion gender sexual orientation gender identity national origin disability or veteran status. Required Experience: Exec Key Skills Change Management,Financial Services,Growing Experience,Managed Care,Management Experience,Analysis Skills,Senior Leadership,Performance Management,Process Management,Leadership Experience,negotiation,Analytics Employment Type : Full-Time Experience: years Vacancy: 1

Under general supervision, implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. You will support one or more products from a regional regulatory perspective. Plan and manage regulatory

The Litigation Lawyer Role: Contentious probate Injunctions Property litigation Negotiating and drafting documentation Shareholder and partnership disputes Employee disputes, regulatory and contractual disputes Assist and supervise junior members of staff where required Play an active role in busin

Regulatory Affairs Manager All the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description. Location: Cambridgeshire Employment Type: (Full-time: Mon-Fri) (Hybrid: 2 - 3 days on site) We are seeking an experienced Regulatory Affairs Manager to lead global regulatory activities across a product portfolio and ensure the products remain safe, effective, and compliant for worldwide xwzovoh markets. This is an exciting opportunity for a proactive regulatory professional to sh... JBLK1_UKTJ

Your new company In order to make an application, simply read through the following job description and make sure to attach relevant documents. You will be joining a leading sterile pharmaceutical manufacturing organisation based in the United Kingdom, recognised for its high standards in quality, compliance, and innovation. The company operates in a dynamic, project-driven environment and is currently expanding its validation team to support new product introductions xwzovoh and ongoing regulatory activities. Your new role As a ... JBLK1_UKTJ

Quality & Compliance Coordinator Are you the right candidate for this opportunity Make sure to read the full description below. Cambridge (hybrid) Up to £32,000 + Benefits A growing organisation in the healthcare sector is seeking a Quality & Compliance Coordinator to support day-to-day Quality & Regulatory Affairs activities. This role is ideal for someone early in their career who brings strong xwzovoh organisation, attention to detail, and an interest in quality systems, auditing, and ISO standard... JBLK1_UKTJ

As they continue to expand their global regulatory footprint, we have an exciting opportunity for an RAQA Manager to join their growing team. As the new RAQA Manager, you will take ownership of regulatory compliance and market access activities across UKCA, FDA, and upcoming CE marking, while overse

Cellcraft is a B2B cultivated meat company based in Cambridge tackling global food security and sustainability challenges. Our AI-driven bioelectronic technology powers the Cellcraft Farm: an end-to-end scalable Cultivated Meat (CM) Manufacturing Platform to empower food producers to make their own delectable sustainable cultivated meats locally. Cellcraft is the worlds first cultivated meat company with a focus on software and analytics. We believe the future of meat must be both sustainable and irresistible. As a Bioprocess Engineer you will play a key role in developing optimising and scaling bioreactor-based processes for cultivated meat production. You will be adaptable and able to handle a range of cross-functional projects in other functional areas including cell line and media development assay development and downstream processing to ensure robust efficient and scalable production systems. Cellcraft is a fast-paced environment. You must be a problem solver capable of applying initiative who enjoys seeing their ideas come to fruition. • Design and execute bioprocess experiments for the development and optimisation of single cell and aggregate cell cultivation in stirred tank and 3D bioreactors., • Develop and implement process control strategies (pH dissolved oxygen feed strategies agitation etc.) to maintain robust cell growth and differentiation., • Lead maintenance and suspension adaptation of cell lines to enable scalable bioprocessing., • Support translation of laboratory-scale processes into scalable manufacturable systems., • Support process transfer scale-up and tech transfer to manufacturing partners., • Analyse process data generate technical reports and present findings to internal stakeholders., • Contribute to and evaluate bioreactor system design including hardware sensors and automation integration., • Bachelors or Masters degree in Biology Bioprocess Engineering Biotechnology or a related field., • A PhD or equivalent industrial experience in cell culture bioprocessing fermentation or related biomanufacturing environments., • 3 years hands-on experience in setting up and operating stirred tank bioreactors in cell therapy biologics or food biotech., • Proven hands-on expertise in aseptic adherent and suspension cell culture techniques., • Strong knowledge of mammalian cell biology growth kinetics bioreactor design and process scale-up., • Hands-on experience with bench-scale bioreactors, • Strong knowledge of measurement optimisation and scaling of bioreactor parameters including mass transfer (kLa) pH temperature agitation (tip speed power input) shear force metabolomics etc., • Experience with process analytical technologies (PAT) automation and process modelling, • Strong analytical problem-solving and data interpretation skills., • Design and operation of continuous perfusion within bioreactor systems, • Culture of induced pluripotent stem cells and other immortalised cell lines, • Knowledge of myogenic and adipogenic differentiation, • Tissue engineering including 3D organotypic culture., • Experience with media and cell line development, • Understanding of computational modelling of fluid dynamics cell growth and other phenomena within bioreactors, • Sourcing and procurement of materials and equipment for bioreactors, • Competitive compensation and stock options, • Private health Insurance, • Potential for excellent career progression, • Exposure to an up-and-coming disruptive and innovative market Cellcraft is an Equal Opportunities Employer. We are committed to creating inclusive teams and providing a work environment that allows all to be themselves. Our Values COMPASSIONATE DRIVE We put people at the core of our push for change. Focusing on the needs of living beings and our planet rather than indulging in the abstract. We embody this without compromise every single day. INVENTIVE VISION We foster a highly innovative environment accelerating creativity and novel ideas which deliver inventive and refreshing solutions for good. We are going against the grain: advocating visionary ideas which disrupt the status quo. We endorse revolutionary thinking and doing. SCIENTIFIC RIGOUR Science is the pursuit of the uncompromising truth and so this is where we have set the bar in all aspects. At our company scientific rigour is not just a value - it is a superpower. Our attention to details and meticulous testing is the secret sauce that make our technologies so mouth-wateringly good. POLYMATH SPIRIT Our work demands myriad skills and expertise enabling us to deliver impact to our partners holistically across their complex value chains. We value the insights arising from different backgrounds and our current team comprises members from many different nations with expertise across multiple disciplines - from bioelectronics to fluid dynamics. Key Skills ASP.NET,Health Education,Fashion Designing,Fiber,Investigation Employment Type : Employee Experience: years Vacancy: 1 Yearly Salary Salary: 45000 - 60000

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference. Every member of Gileads team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future you are the key driver in evolving our culture and creating an environment where every employee feels included developed and empowered to fulfil their aspirations. Join Gilead and help create possible together. Job Description As a Director in the Regulatory and R&D Quality Systems organization you are a thought leader and partner for Regulatory Affairs and R&D Quality stakeholders focusing primarily on regions outside of the U.S. to bring visibility into requirements that will directly support business processes and users in those regions. It requires a good understanding of current technology trends with a keen eye on innovation to help drive change in how technology can continue to transform and support the business in meeting key corporate objectives. Cambridge or Stockley Park onsite 3 days a week. Main Responsibilities: * Provide expertise guidance and leadership in Regulatory Information Management (RIM) Submission Management Inspection Readiness and AI technologies while applying an enterprise mindset. * Manage escalations during critical system issues/outages liaison with IT and Business to ensure impact is clear and support timely communication to end users through resolution. * Operate as a representative for Development Systems during inspections and audits as applicable. * Mentor and guide other Development Systems team members in the U.K. on cross-functional projects. * Work with the team and leaders across geographic regions to ensure support and functional needs are met. * Serve as primary driver and knowledge resource within the team on system evaluation of new or improving technologies to more efficiently meet changing business needs. * Serve as subject matter expert on cross-functional requirement gathering and implementation teams. * Provide strong leadership and engagement with senior leaders internal and external partners and stakeholders. * Provide strategic input to future planning and development of the Development Systems Department. * Oversees or otherwise leads specific projects and /or acts as a core project team member * Interact frequently with other functional areas (i.e. Regulatory Affairs R&D Quality Patient Safety IT). * Represent Development Systems as a technical subject matter expert and contact for projects. Requirements: • BA or BS degree in a scientific discipline information systems or equivalent with a 12 years managing Regulatory Affairs systems or related experience or a MS degree in a scientific discipline information systems or equivalent with 10 years managing Regulatory Affairs systems or related experience., • Proven track record of driving change and strengthening capabilities in complex multi-functional organizations by introducing new technologies and processes Works with minimal direction and exercises latitude in determining technical or business objectives of assignments. * Solid understanding of change management methodology and execution. * In-depth experience in Regulatory Information Management technologies and how the industry is transforming with AI and other innovative technologies. * Good understanding of computer system validation methodology development and execution. * Extensive relevant experience in the pharmaceutical/biotechnology industry including both global and regional roles particularly in Regulatory Affairs and/or R&D Quality * Highly driven self-starter taking personal ownership and initiative with an ability to navigate through ambiguity; exhibit resourcefulness and provide prioritization and focus * Exhibit solid leadership skills with an ability to set a clear vision goals and objectives to inspire and drive innovative thinking and influence across functions * Experience working with cross-functional teams is required. * Exceptional interpersonal skills including teamwork facilitation and negotiation. * Demonstrated experience organizing ad hoc teams to achieve accelerated results. * Excellent planning and organizational skills. Persuasive writer with strong verbal communication skills. * Demonstrated ability to apply technical knowledge to oversight troubleshooting and training. It is the policy of Gilead Sciences Inc. and its subsidiaries and affiliates (collectively Gilead or the Company) to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law all employment actions relating to issues such as compensation benefits transfers layoffs returns from layoffs company-sponsored training education assistance social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds which may include an individuals gender race color national origin ancestry religion creed physical or mental disability marital status sexual orientation medical condition veteran status and age unless such protection is prohibited by federal state municipal provincial local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws. Please apply via the Internal Career Opportunities portal in Workday. Required Experience: Director Key Skills Laboratory Experience,Vendor Management,Design Controls,C/C++,FDA Regulations,Intellectual Property Law,ISO 13485,Research Experience,SolidWorks,Research & Development,Internet Of Things,Product Development Employment Type : Full-Time Experience: years Vacancy: 1

The world isnt standing still and neither is ATS Life Sciences - We dont follow the trends. We set them! Are you interested in being part of a team that makes a difference Join our growing ATS Life Sciences Systems team a division of ATS Corporation a publicly traded global enterprise with a proud history we are helping advance the future with our factory-wide automation solutions. Within Life Sciences Systems what we do matters we custom design build and service critical automated solutions for medical device and pharmaceutical companies. We are dedicated to assisting our customers in improving the quality of life for people around the world. When there is no room for error and product failure is not an option leading life sciences companies trust us to resolve their production challenges. Lead inspire and manage a growing dynamic and high performing engineering department of approximately 80 employees. Engage on critical projects as assigned by General Manager. • Provide subject matter expertise within agreed-upon timeframes to Sales and Applications in the quotation process., • Recommend and implement metrics on customer satisfaction. During the life cycle of large system projects maintain overall customer satisfaction by anticipating and preventing issues before they become customer concerns and by optimizing the use of resources., • Persuade key technical personnel at the customer site that ATS is key to their success to influence subsequent buying decisions. Provide timely customer intelligence to Sales and Business Development. Monitor and report on internal customer satisfaction data to the General Manager., • Implement the departmental policies and objectives as prescribed by the General Manager. Recommend departmental operating budget and operate department within the budget parameters., • Maintain an accurate project status tracking system. Collect monitor and report on performance at the department level for accountable discipline. Ensure optimal utilization of resources., • Accountable for the successful execution of the projects. Resolve issues between different groups at the director level., • Perform SWOT analysis on department as required by the General Manager., • Recommend and implement best practices and standard designs to improve quality. Direct the implementation of 6 sigma lean and continuous improvement projects. Measure and report on quality performance data., • Assist with continuous systems design improvements on production machines., • Direct the assessment of new technology to meet anticipated customer requirements as authorized by the General Manager. Perform SWOT analysis on strategic third party suppliers. Oversee the development of innovative programs to meet industry demand. Recommend and implement design and engineering procedures and standard practices to comply with industry specific regulatory requirements., • Communicate implement and refine the project team culture as prescribed by the General Manager., • Execute the manpower resource and development plan for stratum 2 and set the context for resource planning at the stratum 1 level. Assign projects to stratum 2 managers based on availability skill set and team dynamics., • Make recommendation and refinements to job description competency models compensation strategy pay scales and office layout., • Implement comprehensive performance reviews for direct reports. Produce succession candidates for the Director and Manager roles using the ATS process., • Ensure that all business activities are performed with the highest ethical standards and in compliance with the ATS Code of Business Conduct., • Demonstrate leadership in Health Safety and Environment compliance., • Hold team members accountable for health safety and environmental compliance as part of the annual performance review process., • Ensure that the requirements of the health safety and environment management system are implemented and maintained., • Carry out hazard assessments inspections and audits as required by legislative framework and/or corporate requirements., • Ensure that training is provided to all departmental employees are per established in the training matrix., • Implement appropriate corrective measures for unsafe conditions and unsafe acts., • Ensure that appropriate equipment materials and protective devices are provided and maintained in safe condition., • Provide information instruction and supervision to employees., • Take every precaution reasonable in the circumstances for the protection of employees., • Attend HSE Due Diligence for Management training sessions Education: A post-secondary technology diploma or engineering degree. Experience: Ten years of experience in the design and implementation of complete industrial automation projects. This includes hands-on experience in design build integration of Custom Automation Assembly and Test Equipment. Good written and oral communication skills and ability to lead or work as part of a multi-disciplinary project team are essential. If youre excited about this role but do not meet all the qualifications listed above you are still encouraged to apply Why YOU should join our ATS Life Sciences Systems team: We value our PEOPLE - The foundation of a great company is having the best team which is why we continuously work to develop engage empower and energize our people. The best people want to work with the best team - the best teams are diverse and inclusive teams. What we do MATTERS - our Life Sciences projects contribute to improving the lives of people around the world! ATS has made a commitment to be carbon neutral by 2030! INNOVATION and PROBLEM SOLVING is at our core - Our pursuit of continuous improvement in everything we do. Our focus is on building diverse teams stimulating innovation by challenging conventional thinking encouraging fresh ideas and promoting creative problem-solving We prioritize internal GROWTH & DEVELOPMENT - ATS offers endless opportunities for professional growth and development with a tuition reimbursement program individual development programs and a commitment to promoting from within - there is space for you to grow your career at ATS! We offer COMPETITIVE Total Rewards - Competitive starting salaries overtime pay eligibility paid vacation Employee Incentive Bonus program comprehensive health and dental benefits including Lifestyle Spending Account 5% RRSP matching program and optional Employee Share Purchase Program A place to BELONG: We celebrate our differences and ensure that all employees have equal opportunities for growth and development. We believe that diversity of thought background and experiences is essential for our success and innovation. ATS is in compliance with the Accessibility for Ontarians with Disability Act (AODA) 2005 and will upon request assist those who may require specific accommodations due to a personal disability. We would ask that those who require assistance to notify our offices as soon as possible if accommodation is necessary Required Experience: Director Key Skills Go,Lean,Management Experience,React,Node.js,Operations Management,Project Management,Research & Development,Software Development,Team Management,GraphQL,Leadership Experience Employment Type : Full Time Experience: years Vacancy: 1

Job Description The Onyx Research Data Platform organization represents a major investment by GSK R&D and Digital & Tech designed to deliver a step- change in our ability to leverage data knowledge and prediction to find new medicines. We are a full-stack shop consisting of product and portfolio leadership data engineering infrastructure and DevOps data / metadata / knowledge platforms and AI/ML and analysis platforms all geared toward: * Building a next-generation data experience for GSKs scientists engineers and decision-makers increasing productivity and reducing time spent on data mechanics. * Providing best-in-class AI/ML and data analysis environments to accelerate our predictive capabilities and attract top-tier talent. * Aggressively engineering our data at scale to unlock the value of our combined data assets and predictions in real-time A Senior Governance Engineer is a leading technical contributor who can consistently take a loosely defined business or technical requirement architect and build it to a well-defined specification and execute on it at a high level. You have a strong focus on metrics both for the impact of their work and for its inner workings / operations. As a Senior Governance Engineer you will play a crucial role in ensuring our product teams produce reliable scalable and secure infrastructure and applications. You will collaborate closely with the platform infrastructure and data operations teams to implement security and governance products within our existing technological infrastructure. You should be deeply familiar with the tools and processes associated with security and governance for regulated industries and able to work with stakeholders to translate those requirements to build efficient and user-friendly products. * Design and deploy scalable and reliable governance solutions using a mix of existing technologies open-source tools and newly identified integrations. * Build and maintain an automated policy engine that integrates with existing authorization systems uses policy as code is cloud-native (GCP) and integrated with the other Onyx Platforms and frameworks. * Enable governance by design and implementation of user-friendly products through the use of computational and automatable engines and integrations with existing data platforms and pipelines metadata and authorization systems. * Understand amplify with Onyx and integrate requirements from security and internal regulatory teams to ensure compliance with security policies and regulations as part of the governance products. * Collaborate with cross-functional teams to understand business requirements and translate them into scalable and efficient governance products. * Use standard agile development SDLC processes for development management CI/CD and automation for infrastructure provisioning and deployment processes. * Stay updated with the latest trends and best practices in security governance and data governance and contribute to the continuous improvement of our overall infrastructure and data platform. * Provide technical guidance and mentorship to junior team members fostering a collaborative and knowledge-sharing culture within the organisation. * Troubleshoot and resolve governance related issues and provide technical support to internal teams. We are looking for professionals with these required skills to achieve our goals: * Bachelors degree. * Knowledge and use of one or more programming languages: e.g. Go Python Scala Java. * Experience in utilizing any cloud-based data governance solutions like Open Policy Agent (OPA) Strya-DAS Immuta Privacera Gatekeeper AWS Data Governance tools Google Cloud Data Catalog/DataPlex or Microsoft Azure Purview to manage and govern data across various cloud environments. * Experience with Policy and Compliance monitoring. If you have the following characteristics it would be a plus: * Extensive knowledge of computational data governance data security compliance regulations and industry best practices. * Experience with managing authorization and authentication as code integrating with Enterprise role-based access tools. * Experience with implementing attribute-based access control. * Demonstrated experience building reusable components on top of the CNCF ecosystem including Kubernetes (or similar ecosystem) * Experience in modern software development tools / ways of working (e.g. git/GitHub devops tools metrics / monitoring ) * Cloud experience (e.g. AWS Google Cloud Azure Kubernetes) including infrastructure-as-code * Application experience of CI/CD implementations using git and a common CI/CD stack (e.g. Jenkins CircleCI GitLab Azure DevOps) * Demonstrated excellence with agile software development environments using tools like Jira and Confluence * Passionate about data-management and governance/privacy best practice #GSK-LI If you are based in Cambridge MA; Waltham MA; Rockville MD; or San Francisco CA the annual base salary for new hires in this position ranges $136950 to $228250. The US salary ranges take into account a number of factors including work location within the US market the candidates skills experience education level and the market rate for the addition this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family) retirement benefits paid holidays vacation and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country the relevant compensation will be discussed during the recruitment process. Why GSK Uniting science technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale. People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law. We believe in an agile working culture for all our roles. If flexibility is important to you we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on ___

Tesco Travel Money Advisor Cambridge Bar Hill Part Time Job Type: Permanent Hours per week: 18 hours Salary: 13.00 per hour Monthly Bonus Working Patterns: This job is perfect for those who are flexible and able to work a variety of shifts between Monday to Sunday. Benefits: * A wide range of insurances such as Private Medical Dental and Critical Illness. It also includes discounted products such as Health Checks (Screens) Allergy Intolerance and Other Health Tests. * Employee wellness programmes that offer guidance and tips on all aspects of wellbeing such as physical mental and financial. * A wide range of employee discounts provided by Bravo Benefit * Flexible hours and shift patterns to suit a variety of lifestyles with opportunities for overtime * 25 days holiday (pro-rata). Bank holidays and the opportunity to gain more days the longer you are a part of Travelex as well as the option to sell days * Opportunity to earn a monthly bonus on top of base salary for hitting targets * Pension with a great Pension Provider Scottish Widows. Exchange your job for a new career with limitless destinations at Travelex. Travelex attributes its success and growth down to its hard-working people. Its their desire to deliver exception results service and positive experiences to our customers every day that sets us apart from the rest. If you identify yourself as someone who truly cares about providing exemplary service loves to travel and enjoys sharing your knowledge and experience with others then we want you as our next Travel Service Partner (RSA). As an integral part of the Tesco Team you will be placed at the heart of a bustling Retail environment supporting our retail customers with their Foreign Exchange options and ensuring that their travel experience starts off in the best way possible. What will you be doing * Nurturing and forming relationships with customers to gain a better understanding of their travel * Establishing yourself as a travel money ambassador and their trusted advisor providing support and advice on great Travelex products and services * Engaging with customers to process all foreign exchange transactions accurately and efficiently. * Delivering on key performance goals both procedural operational and customer focused * Utilising your keen eye for detail to process daily online FX request and deliveries * Implementing best practice legal and regulatory standards and adhering to Travelex compliance procedures What do I need to have * Great Communicator - Youll find talking with people and building relationships comes naturally to you. Youll not only be a great talker but a good listener who is understanding of people and their needs. * Desire to succeed Youll have the drive and vision to want to make a difference to enjoy what you do care about the impact you have and the way you make people feel. Please note as part of the onboarding process you will be required to clear our reference check company standards. We have a dedicated team who will support you through this process. About Travelex We are one of the market leading specialist providers of foreign exchange. Founded in 1976 and differentiated by our brand and market footprint over the past 45 years we have built a network of foreign exchange stores and developed Travelex as a trusted and widely recognised brand in international money. Our mission is to simplify our customers access to international money however and whenever. Exciting We think so! Your journey starts here so take the first step to become part of the Travelex Team by clicking apply! We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race religion colour national origin gender sexual orientation age marital status veteran status or disability status. #EastEngland Required Experience: Unclear Seniority Key Skills Channel Marketing,Accounting Tally,CSS,Corporate Risk Management,Hibernate,Brokerage Employment Type : Part-Time Experience: years Vacancy: 1

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Senior Clinical Team Manager PPDs (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between its you! We know that meaningful results not only require the right approach but also the right people. We invite you to re-imagine health promoting protocols with us working alongside our talented bright and energetic teams. Our Project Delivery team directs coordinates and manages the technical and operational aspects of projects securing the successful completion of clinical trials. The team is therapeutically aligned to respond better to our customer needs. The therapeutic scope includes Cardiovascular & Internal Medicine- This need is for Nephrology experience in particular as well as dermatology GI (UC/CD) Cardiovascular Liver Nephrology Immunology Rare Disease Diabetes Obesity Dyslipidemia Womens Health Rheumatology (RA SLE Gout). We are currently looking for experienced CTMs who have worked in Nephrology & Transplant as well as NASH & Dermatology. As a Senior Clinical Team Manager (CTM) you combine deep knowledge therapeutic expertise and robust tools to help our clients deliver life-changing therapies to market. You take ownership anticipate problems find solutions and deliver results. You take ownership anticipate problems find solutions and deliver results; coordinating the activities of Clinical Management members which are allocated to a project on a Regional or Country basis. You will work in partnership with the Project Manager to ensure the necessary training tracking and quality systems are in place for the clinical management team and be primarily responsible for the clinical deliverables of the Project within agreed timelines and budget. Clinical Team Managers provide contact and support to the project sponsor for all clinical aspects. At PPD we hire the best develop ourselves and each other and recognize the power of being one team. We offer continued career advancement opportunities award winning training and benefits focused on the health and wellbeing of our employees. Summarized Purpose: Accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. Interprets data on complex issues and makes good business decisions with support from line management. Works to ensure that all clinical deliverables meet the customers time/quality/cost expectations. Maintains profitability by ensuring clinical activity is conducted within contract scope through efficient management of the clinical team. Typically works independently on projects of moderate to high complexity and may assume regional lead or Clinical Study Manager responsibilities. Essential Functions: • Manages all clinical operational and quality aspects of allocated studies of moderate to high complexity in compliance with ICH accordance to project specific requirements may assume Lead CTM responsibilities on regional level Clinical Study Manager (CSM) responsibilities or take on additional responsibilities; e.g. process improvements manage complex programs have wider management or project coordination responsibilities., • Develops clinical tools (e.g. Monitoring Plan Monitoring Guidelines) in conjunction with the Data Quality Plan. Contributes to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensures timely set up organization content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs CRF guidelines patient informed consent templates and other protocol specific documents as required. Collaborates with the project manager to prepare organize and present at client meetings including bid defense and hand-off meetings., • Collaborates with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicates with the team and leads team meetings to ensure that timelines resources interactions and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department., • Ensures achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics providing status updates to the project manager regularly reviewing projects using tracking and management tools implementing recovery actions reviewing monitoring visit reports and managing CRF collection and query resolution. Continuously monitors clinical trials to assess performance and ensure contractual obligations are met. May routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials., • Communicates with study sites regarding issues such as protocol patient participation case report form completion and other study-related issues., • May coordinate all start-up activities and ensures that essential document quality meets the expectation of Regulatory Compliance Review. Ensures timely regulatory submissions (if appropriate) are addressed. Reviews and follows up on all questions raised by ethics committees. Responsibilities may vary based on project timelines., • Bachelors degree or equivalent and relevant formal academic / vocational qualification, • Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 5 years)., • Strong leadership skills effective at mentoring and training and capable of motivating and integrating teams, • Strong planning and organizational skills to enable effective prioritization of workload and workload of team members, • Strong interpersonal and problem-solving skills to enable working in a multicultural matrix organization, • Solid understanding of change management principles, • Comprehensive understanding of the practices processes and requirements of clinical monitoring, • Strong judgment decision making escalation and risk management skills, • Effective oral and written communication skills including English language proficiency, • Capable of evaluating own and team members workload against project budget and adjust resources accordingly, • Strong financial acumen and knowledge of budgeting forecasting and fiscal management, • Strong attention to detail, • In-depth understanding of relevant regulations e.g. ICH/GCP FDA guidelines etc., • Strong computer skills to effectively use automated systems and computerized applications such as Outlook Excel Word etc., • PPD a part of Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:, • Able to communicate receive and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner., • Able to work upright and stationary for typical working hours., • Able to work in non-traditional work environments., • Able to use and learn standard office equipment and technology with proficiency., • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities., • May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments., • Integrity Innovation Intensity Involvement, • If you resonate with our 4i values above and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the worlds most urgent health needs submit your application wed love to hear from you! We are unable to consider junior applications at this time. Required Experience: Manager Key Skills Dermatology,Marketing and Merchandising,Corporate Risk Management,Kpo,Accident Investigation,Content Management Employment Type : Full-Time Experience: years Vacancy: 1

As the Head of Customer Delivery youll get to shape and scale our customer delivery operations as we grow. Our commercialisation is gaining rapid momentum; so this role is a key strategic hire for our business. Youll be part of the senior management team overseeing successful deployments commissioning and lifecycle support of complex automation systems for our global customers. What Youll Do • Youll get to define and lead the end-to-end customer delivery strategy from design and build through to installation validation training and handover., • Youll build and inspire a high-performing team covering project management commissioning and field service., • Youll oversee complex multi-stakeholder delivery programmes ensuring excellence in governance risk management and communication., • As the senior point of contact for customer delivery youll lean on your ability to nurture trust-based relationships with major global partners., • Youll drive continuous improvement in delivery quality and reliability as the champion of the customer voice within Cellular Origins. Qualifications : Youre a proven technical leader whos delivered complex systems into regulated manufacturing environments (GMP/biopharma preferred). Youre comfortable navigating ambiguity aligning diverse stakeholders and building the structures that turn ambition into execution. Key requirements: • Degree in Engineering Biotechnology or related field (BSc/MSc)., • PRINCE2 PMP or equivalent programme management credentials., • Significant experience delivering high-CAPEX automated systems in regulated sectors., • Proven ability to influence senior leaders in major customer organisations., • Strong leadership skills and experience building high-performing teams., • Deep understanding of system integration validation and regulatory requirements., • Excellent communication and stakeholder management skills., • Experience working within ISO 9001 or similar quality systems., • Willingness to travel (approx. 10%). Additional Information : Our employee benefits include: • Annual profit-related bonus, • 25 days holiday, • Employer pension contribution of 10% of salary, • Free lunch and all-day refreshments, • Private medical insurance for employees and dependants, • Enhanced family friendly leave, • Life insurance worth 6x salary, • Electric car leasing scheme, • Cycle to work scheme, • Season ticket loan, • A fund that supports healthy activities that bring colleagues together; whether its lunchtime squash or football board games or our own rock band. Colleagues initiate new clubs and outings whenever they feel theres something missing! Every application will be reviewed by the hiring team and will receive a response. Remote Work : No Employment Type : Full-time Key Skills Civil Engineering,Communication,Corporate Partnerships,Fire Fighting,Business Analytics,ACCA Experience: years Vacancy: 1

Avantor is seeking a dedicated and experienced Laboratory Technician Service Lead to join our team in Cambridge UK. This is a key management role within our on-site solution where you will oversee the Laboratory Technician Support this role you will manage and mentor a team of Laboratory Technicians (up to 14 direct reports). This is a 12-month fixed-term position based in a state-of-the-art facility at the Discovery Centre BioMedical Campus in Cambridge. Alongside an attractive salary we offer a comprehensive benefits package including a bonus a pension scheme private medical and dental care and an additional day off for your birthday. Working hours: Monday to Friday core hours The Team You will join a team of three Laboratory Service Leads each with expertise in different laboratory disciplines. Youll be responsible for leading and mentoring a team of Laboratory Technicians (up to 14 direct reports) based in research and development laboratories. What were looking for Education: • A Bachelors degree in a scientific discipline or equivalent experience in a laboratory environment Experience: • People management including recruitment behavioural management and staff development, • Laboratory experience including knowledge of SHE requirements in a laboratory setting with IOSH certification being desirable, • Familiarity with GLS GxP regulations audit requirements and CAPAs, • Incident response and investigation including root cause analysis (RCAs), • Proficient in Microsoft Excel and data analysis/reporting, • Experience in writing Risk Assessments and COSHH How youll thrive and create an impact • Oversee day-to-day laboratory operations supporting a team of Laboratory Technicians to ensure smooth and efficient lab operations, • Take responsibility for all aspects of Health and Safety including audits and GEMBA walks and ensure regulatory compliance, • Plan and manage time throughout the day prioritising and coordinating the execution of daily operational tasks for the scientific support team, • Attend regular business meetings with customers to present data including KPI capture and analysis of any deviations, • Create maintain and update relevant documentation to support service delivery compliance and training such as work instructions risk assessments COSHH assessments and training #LI-Onsite Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor Dare to go further in your career. Join our global team of 14000 associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes peoples lives for the better. It brings new patient treatments and therapies to market giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his moms voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex gender identity sexual orientation race color religious creed national origin physical or mental disability protected Veteran status or any other characteristic protected by federal state/province or local law. If you need a reasonable accommodation for any part of the employment process please contact us by email at ___

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Location/Division Specific Information This role will be embedded within a client dedicated team. You will work alongside the clients own experienced personnel as well as PPD colleagues to deliver innovative clinical support with non interventional studies. Summary of Essential Functions : • Responsible for the delivery of the cross-functional project (time cost quality) by working closely with Global trial and functional leads, • Ensures escalation pathways adhered to internally and externally (Rules of Engagement communication pathways)., • On projects where the scope requires ensures clear delineation in responsibilities and communication pathways for secondary project leads (such as lead in a specific region lead for a specific vendor(s) or subset of delivery)., • Ensures financial stewardship at a trial level by demonstrating an intimate understanding of the contract resource alignment to budget management of Out-of-Scope activity drive the Con Mod process/negotiations and team execution to timelines., • Establishes communicates and manages customer expectations to achieve optimal delivery during the project, • Drives Risk Identification and Issue Resolution at project level, • Ensures project team compliance with organization policies SOPs ICH- GCP regulatory and project specific requirements., • Responsible for vendor management where required, • Ability to delegate and effectively prioritize own and workload of project team members in a frequently changing environment, • Effective oral and written communication and presentation skills, • Proactive solutions oriented and adaptable to changing priorities and situations, • Advanced therapeutic area knowledge and clinical development guidelines and directives, • Sound interpersonal and customer service skills including the ability to lead motivate and coordinate cross-functional project teams, • Ability to negotiate persuade and influence others including a cross cultural awareness Education and Experience: • Bachelors degree or equivalent - Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 8 years) with 2 years of project/trial management. Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000 colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory with PPD part of Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued. Apply today! Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status. Required Experience: Senior IC Key Skills Administrative Skills,Facilities Management,Biotechnology,Creative Production,Design And Estimation,Architecture Employment Type : Full-Time Experience: years Vacancy: 1

Are you an experienced extra high voltage or high voltage engineer Do you want to push the boundaries of your profession and develop in an open collaborative and empowering culture Are you looking for an exciting new challenge If this sounds like you or youre curious to learn more then this role could be the perfect opportunity. Join our Transmission and Distribution Department as our new Associate Consultant (m/f/x) and work with us to close the gap to a sustainable future. Your new role The principal function of this position is to lead and oversee electrical design activities within the team as directed by the Head of T&D and to assist in the development of the Groups capabilities in the field of HV/EHV Engineering. The role will include taking a senior role in project work focused on production and client liaison mentoring and coaching junior members of the team. The role includes meetings with clients contractors and other designers. It is therefore important the candidate has good communication skills and can demonstrate relevant experience. Site visits or visits to non-UK design offices will also be required during design and delivery. The role involves taking responsibility for Work Package Design Management including all reporting to satisfy the companys design management requirements. In this exciting role you will play a pivotal part in the expansion of our UK sector within the Transmission & Distribution (T&D) business leveraging our global delivery and growth model. As a member of the UK T&D team you will be integrated into our dynamic global Power Systems team which boasts a robust network of 300 highly skilled engineers. Our team possesses specialized expertise in substation design cable engineering and overhead line design. You will collaborate closely with our seasoned professionals in these areas leading and innovating design projects for the UK market. Additionally you will have the transformative opportunity to support and cultivate the development of our UK design team contributing to its growth and success. Join us in shaping the future of power systems and make an impactful difference in the industry! Your key responsibilities will be • Lead role for one of the key electrical disciplines based on your professional background: 1) Primary 2) Secondary Design 3) OH or 4) Cable design of HV and EHV Substations in compliance with relevant BS IEC and customer-specified standards., • Responsibility for coordination of design of substation and/or OH/cable design from concept to detailed design as per client requirements., • Multidisciplinary design management., • Liaison with other members of the design team and client engineers., • Technical management of junior engineers and CAD draught professionals., • Calculation of loading and short-circuit values of primary plant., • Accountable for approving primary engineering design on own projects as well as for other team members. Attend technical meetings with the client to ensure client satisfaction., • HNC / HND / Degree Qualified in Electrical Engineering with experience in the UK Electricity Transmission and Distribution industry. Ideally NG authorised., • Membership of the IET Chartered Status or working towards Chartered Engineer status., • Experience of working and/or authorisation with major UK utilities such as NG or DNO companies. Possess a proficient understanding of the electricity industry & regulatory standards policies and their application to the role., • Strong electrical knowledge and experience in the equipment design specification layout and detailed engineering of extra and high voltage substations electrical equipment and product range., • A good understanding of electrical plant transformer protection relays and control principles and construction disciplines and current ENA BS and IEC electrotechnical engineering standards to ensure full application and compliance requirements can be achieved., • Multi-disciplinary design management experience., • An ability and willingness to work in a multi-disciplinary and multi-locational team environment in collaboration with our clients., • Dedicated to a Net Zero future. What we can offer you • Commitment to your development., • Leaders guided by our Leadership Principles., • A culture that welcomes you as the unique person you are., • Inspiration from colleagues clients and projects., • The long-term thinking of a foundation-owned company., • Flexible work environment., • 27 days annual leave plus bank holidays., • Matched pension contributions. Please submit your application and CV online. We invite diversity in all its forms and encourage applicants from all groups to apply. Do you have any questions Contact: Jelena Oka BSc MSc CEng FIET MAPM Head of Transmission and Distribution UK Energy Management M: Work at the heart of sustainable change with Ramboll Ramboll is a global architecture engineering and consultancy company. As a foundation-owned people company founded in Denmark we believe that the purpose of sustainable change is to create a thriving world for both nature and people. So thats where we start and how we work. Our history is rooted in a clear vision of how a responsible company should act and being open and curious is a cornerstone of our culture. Ramboll employs more than 18000 people globally across 35 countries. Ramboll experts deliver innovative solutions across Buildings Transport Water Environment & Health Energy Management Consulting and Architecture & Landscape. Combining local experience with global knowledge we help shape the societies of tomorrow. Equality Diversity and Inclusion Equality diversity and inclusion are at the heart of what we do. At Ramboll we believe that diversity is a strength and that different experiences and perspectives are essential to creating truly sustainable societies. We are committed to providing an inclusive and supportive work environment where everyone is able to flourish and reach their potential. We also know how important it is to achieve the right balance of where when and how much you work. At Ramboll we offer flexibility as part of our positive and inclusive approach to work. We invite applications from candidates of all backgrounds and characteristics. Please let us know if there are any changes we could make to the application process to make it more acceptable for you. You can contact us at with such requests. Remote Work : No Employment Type : Full-time Key Skills Engineering Support,MAC,Hydraulic,General Services,Ado,Health Education Experience: years Vacancy: 1

Are you a confident relationship builder with a passion for helping brokers grow their business Do you thrive in a fast-paced people-first environment where no two days are the same If so this could be your next move. At Aldermore were all about enabling more people to go for it - whether thats buying a home growing a business or saving for the future. As our Business Development Manager youll join a high performing region to play a key role in driving new business and championing our award-winning mortgage proposition across the East of England. Location:CB CM CO IP NR RM SG SS To apply you must live within this area as the role requires regular face-to-face meetings with brokers across the region. What will your day look like Youll be the face of Aldermore for your panel of brokers out on the road and on the phone. Building trusted relationships providing expert support and helping them find the right solutions for their clients. Your mission To deliver exceptional service and hit ambitious new business targets through high-quality mortgage acquisitions. • Develop and grow relationships with brokers across your region, • Drive new business performance and achieve key sales KPIs, • Collaborate closely with your Telephony BDM partner to deliver a seamless broker experience, • Deliver engaging group presentations and product updates, • Stay ahead of the curve with product market and regulatory knowledge, • Be the go-to expert for underwriting queries and criteria changes, • Feed valuable market insight back into the business to shape future strategy What do we expect from you Were looking for a confident proactive and commercially minded professional who knows how to make things happen. • Youll be located within the region; CB CM CO IP NR RM SG SS and have a full UK drivers licence, • Proven B2B sales experience within financial services (preferably intermediary mortgages), • Strong account management and relationship-building skills, • A deep understanding of the mortgage market and broker landscape, • A collaborative can-do attitude with a drive to deliver results, • Excellent communication and presentation skills, • CeMAP qualified (or willing to achieve within 12 months) What can you expect from us • Hybrid working policy, • Car / car allowance and a great range of core benefits and bonus potential, • A friendly and flexible culture the same as how we work with our customers, • A growing organisation that means theres lots of opportunities to progress, • A drive for continuous improvement which you will be empowered to get behind from day one Let us tell you a bit about us Were Aldermore the award-winning bank trusted and highly rated by over a quarter of a million customers for more than a decade. With our range of specialist mortgages savings accounts and business finance solutions were backing more people to go for it. We thrive by saying yes to our customers. We respect the ingenuity of entrepreneurs and their startups; we give first-timers a leg-up onto the property ladder; we open up the lending market to many; and thousands of customers chose MotoNovo Finance every week to buy their next car van or motorbike. This is where you come in. We are on a journey. A journey defined by a destination; to deliver on our purpose. Still curious Join us and well make the same promises to you as a colleague as we do to each of our customers. Were committed to building a working environment that values respect diversity and compassion. We welcome people regardless of age disability gender identity marital status race faith or belief sexual orientation socioeconomic background and whether youre pregnant or on family leave. Please note: we have a thorough screening and referencing process which includes criminal record check The Company We champion equality by supporting the exceptions to the rule and getting finance to where its needed. We lend the money people save with us to people who want to get on in life; build businesses and create employment buy property for people to live and work in and purchase vehicles to move families and goods around. Behaviour Framework Our behavioural framework underpins our purpose and strategic drivers as it outlines the behaviours we need to demonstrate in order to succeed. Where our strategic drivers (Stay Ahead Propositions Relationships That Last and Progressive Platform) outline what we need to do to succeed our behaviours guide us in your second interview well ask you to talk through some examples where youve demonstrated these behaviours in your previous roles. The Benefits As you would expect we offer a competitive basic salary and reward package and youll also benefit from our commitment to investing in your professional development throughout your journey with us. Benefits vary across the business depending on the role you do but these will give you an idea of what to expect: • Discretionary bonus scheme, • Aviva Digital GP, • Bus And Tram Benefit, • Employee Assistance Programme, • Eyecare Voucher & Display Screens/Desk Set-Up, • Flu Jab Vouchers, • Group Income Protection, • Life Assurance, • Metrolink Annual Pass & Clipper Ticket, • Microsoft Discounts, • Private Medical Insurance Shopping Discounts, • Toothfairy, • Your Workplace Pension, • Hybrid Working, • Critical Illness, • Cycle To Work, • Dental Insurance, • Give As You Earn, • Government Tax-Free Childcare Scheme, • Octopus Electric Vehicles, • Save Our Planet, • Season Ticket Loan, • Spouse Or Partner Life Assurance, • Technology, • Wearable Technology, • Wellbeing App Required Experience: Manager Key Skills Business Development,Sales Experience,B2B Sales,Marketing,Cold Calling,Account Management,Territory Management,Salesforce,Affiliate Marketing,CRM Software,negotiation,Lead Generation Employment Type : Full-Time Experience: years Vacancy: 1 Yearly Salary Salary: 50001 - 999999999

Overview: TekWissen is a global workforce management provider throughout the UK Europe and many other countries in the world. The below client is an American multinational pharmaceutical and biotechnology corporation. Job Title: Quality Engineer Location: Cambridge UK Duration: 12 Months WorkType : Hybrid Job Description: • This position is in the Biotherapeutics Pharmaceutical Research and Development Devices Centre of Excellence located in client location., • The incumbent will provide design control and risk management subject matter expertise to medical device and combination product development programmes throughout the product lifecycle., • This will involve generation and review of design history file and risk management file components whilst interacting with cross functional development teams at all levels of the organisation. POSITION RESPONSIBILITIES, • Lead design control and risk management activities for combination product development programs ensuring deliverables are appropriately authored approved and maintained to support clinical trials and commercial licensures., • Support and facilitation of effective risk management activities at external design companies and manufacturing facilities related to assigned projects., • Ensure combination product development activities are compliant with quality and regulatory standards both internal and external., • Provide input and support to design validation including but not limited to human factors engineering assessments., • Support the assessment of external design companies and suppliers for capability of quality systems facilities and procedures to support device development and supply., • Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture., • Support the generation of all regulatory submission data and content for assigned device projects., • Support internal and external audits of the DCoE Quality Management System. EDUCATION SKILLS AND EXPERIENCE, • History of working in accordance with the requirements of ISO 13485 ISOCFR 820 21 CFR 4 and the EU Medical Devices Regulation., • Experience in design controls and risk management for combination products., • Familiar with Human Factors Engineering - Usability Engineering., • Familiar with device assembling manufacturing processes. TECHNICAL SKILLS REQUIREMENTS., • Working knowledge of ISO 9001 ISO 13485 ISOCFR 820 21 CFR 4 and the EU Medical Devices Regulation., • Familiarity with EN 62366 EN 60601 and EN 62304., • Able to learn and apply established procedures in a reliable and consistent manner., • Capable of working independently with minimal supervision., • High level of attention to technical details and accuracy., • Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously., • Able to work collaboratively in cross functional teams., • Excellent communication (e.g. oral written presentation) and interpersonal relationship skills., • Proficiency in general computer software such as word processing spreadsheets presentations., • Understand Good Manufacturing Practices (GMP). PHYSICAL POSITION REQUIREMENTS

Safety HOW MIGHT YOU DEFY IMAGINATION If you feel like youre part of something bigger its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching manufacturing and delivering ever-better products that reach over 10 million patients worldwide. Its time for a career you can be proud of. Join us. SENIOR ASSOCIATE GLOBAL SAFETY LIVE What you will do In this vital role you will be responsible for ensuring adherence to Amgens regulatory commitment for pharmacovigilance. You will perform a wide variety of drug safety activities within the UK and Ireland affiliate working with both local and global colleagues and based on sound knowledge of pharmacovigilance regulations and company procedures. • Pharmacovigilance Legislation: Maintains own current knowledge of and compliance with local safety regulations., • Case management: Perform business critical core safety activities per legal deadlines including intake of AE reports follow up with HCPs for complete data ICSR & aggregate safety report submission to regulators. Handling safety enquiries received to the departmental inbox from both internal and external stakeholders. Review metrics to monitor MHRA & HPRA submission compliance., • Periodic Reporting: Assist with submission of DSUR and PSUR safety reports to Regulators and Ethics Committees where applicable. Perform review of relevant PSUR safety signals for MHRA notification., • Risk Management: Support for safety risk communications (e.g. Dear Investigator Letter Urgent Safety Measures Risk Minimisation Materials etc) and Risk Management Plans in conjunction with Regulatory Affairs Clinical and Medical Departments., • Training: Delivers safety reporting training for local affiliate staff and external service providers., • Key contact: Serves as key contact for defined safety activities within the affiliate. Provides expert safety input into various cross-functional initiatives e.g. Patient Support Programs Market Research Digital Media Projects local Study Protocols etc to ensure compliance while understanding local business needs. Be part of our team You would be joining the UK & Ireland Safety Team based in the local affiliate and collaborating with other affiliate functions and also with Global Patient Safety colleagues to meet business needs. Together with team members you would conduct business critical safety tasks provide support to audits and inspections and assist the Senior Global Safety Manager with activities and issue resolution where necessary. Within the team you would maintain awareness of safety profiles and new risk information for designated Amgen products to support product safety activities. WIN What we expect of you We are all different yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional are these qualifications and skills: • Graduate with life science or healthcare degree and proven relevant industry experience within post market and clinical trial pharmacovigilance., • Use of MS Office products to a proficient standard Word Excel PowerPoint., • Demonstrable knowledge of processes and regulations in pharmacovigilance., • Experience with Safety Databases., • Natural team player with the personal qualities to relate well to people at all levels., • Aptitude for analytical thinking with a methodical approach and unquestionable attention to detail., • Highly motivated quick to learn with ability to work effectively under own initiative and a strong drive for excellence. THRIVE What you can expect of us As we work to develop treatments that take care of others so we work to care for our teammates professional and personal growth and well-being. • Vast opportunities to learn and move up and across our global organization, • Diverse and inclusive community of belonging where teammates are empowered to bring ideas to the table and act, • Generous Total Rewards Plan comprising health finance and wealth work/life balance and career benefits, • Flexible working from home options available Application close date: 21st November 2025 APPLY NOW for a career that defies imagination In our quest to serve patients above all else Amgen is the first to imagine and the last to doubt. Join us. Equal Opportunity Statement Amgen is an Equal Opportunity employer and will consider you without regard to your race colour religion sex sexual orientation gender identity national origin protected veteran status or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request an accommodation. . Required Experience: Senior IC Key Skills Beauty And Fashion,EMC,Jewellery,Arabic English Translation,Business Analytics Employment Type : Full-Time Experience: years Vacancy: 1

Management of Regulatory Affairs personnel through line management and project delivery oversight. Responsible for developing study regulatory strategies and leading department initiatives. The role involves collaboration with other departments to support the successful approval of clinical trials. May have regional-specific responsibilities e.g. Manager Regulatory Affairs Europe. • Review study protocols and informed consent forms to ensure that documents are compliant with applicable regulatory standards and that regulatory and operational risks are minimized., • Manage and review the translation of drug labels in collaboration with sponsors and third-party vendors., • Support study regulatory strategy by:, • Management of regulatory aspects of the study ensuring required approvals are obtained, • Significant contribution to the achievement of study start-up milestones by overseeing and managing high quality regulatory submissions, • Monitor regulatory intelligences sources to ensure that the study remains in compliance throughout the lifecycle of the study, • Identify risks to milestone achievement and propose solutions to mitigate these risks, • Develop and author study Submission Management Plan, • Create and maintain study-specific regulatory trackers and document sharing methods to communicate information to internal and external stakeholders, • Act as first point of contact for all regulatory related communications with the sponsor and internal study team, • Organize and lead regulatory meetings with internal and external stakeholders and participate in cross-functional study team meetings ensuring that timely regulatory updates and issues are discussed, • Maintain efficient collaboration and relationship with external vendors responsible for study applications and oversee tasks delegated to them., • Prepare execute and/or oversee submissions as described in the Submission Management Plan including, • clinical trial applications to regulatory authorities and ethics committees and import/export license applications, • Develop and/or author country-specific Informed Consent Forms, • Perform Quality Check procedures on submissions documents and trackers, • Lead and coordinate responses to information requests from regulatory authorities or ethics committees, • Perform the above activities during study start-up and throughout the lifecycle of the clinical trial with, • amendments notifications annual reports and end of trial submissions ensuring compliance to ICH GCP regional/local requirements, • Problem solve and provide issue resolution to assist the team address unforeseen risks that have the potential to impact the successful delivery of the trial, • Support revenue recognition and other budget-related activities, • Represent the department during audits or inspections and address questions and issues raised by auditors or inspectors, • Mentor and train regulatory colleagues, • Main point of escalation for direct reports with Regulatory Study Lead responsibilities., • Oversee and provide guidance on all regulatory aspects of a study focusing on regulatory tracking issue management timelines and post-approval compliance (e.g. Annual Reporting Notifications)., • Perform Quality Check procedures on submissions documents and trackers, • Study revenue recognition and financial management/budget support., • Back-up and support direct reports with Regulatory Study and Country Lead responsibilities identified above., • Supervise mentor provide leadership and manage career and skill development of direct reports by supporting individual goals and objectives that align with department strategies and individual career ambitions and manage performance to ensure objectives are achieved., • Provide line management for assigned direct reports fostering an environment of curiosity flexibility empowerment accountability and transparency. Encourage a growth mindset., • Continuously gauge the pulse of direct reports and collaborate with other department leaders to evaluate department needs through training learning and development and other engagement-related improvements., • Identify and assess department needs and areas for improvement., • Lead initiatives that are aligned with department and organizational objectives., • Perform gap analyses in response to changing regulations and guidelines., • Initiate change management activities when new or revised regulations and guidelines impact business processes., • Subject matter expert for complex regulatory topics., • Review proposals and study pricing as required., • Participate in bid defenses as requested and when topics are included that align with areas of expertise., • 7 9 years of related experience, • (Honors) Bachelors degree, • Expert knowledge of European regulations across clinical and commercial phases, • Critical thinking and problem solving, • Managing Direct Reports, • Strong time management and organizational skills, • Financial and business acumen, • Difficult and complex communications (technical topics performance and team engagement), • Hands-on experience with regulatory submissions including and post-approval changes, • Skilled in regulatory project management tracking timelines deliverables and dependencies across global teams, • Regulatory intelligence and strategy able to interpret evolving guidelines and guide cross-functional teams accordingly, • Collaborative across functions works closely with clinical safety and medical writing teams, • Detail-oriented execution ensures accuracy compliance and consistency in all regulatory deliverables, • Strong communication and risk assessment skills capable of defending regulatory positions with internal/external stakeholders, • Home-based, • *Accommodations for job applicants with disabilities are available upon request.We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed please contact us. Required Experience: Manager Key Skills Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills Employment Type : Full-Time Experience: years Vacancy: 1

Would you like to apply your Regulatory Affairs strategy expertise and passion to make an impact in a company that follows the science and turns ideas into life changing medicines At AstraZeneca we do this with the upmost integrity even in the most sophisticated situations because we are committed to doing the right thing! We continuously forge partnerships that help bring world-class treatments to patients in new ways combining our peoples outstanding skills with those of people from all over the globe. Within Oncology Regulatory Science Strategy and Excellence (ORSSE) we bring hope and solutions to patients with unmet needs. We work across our ground-breaking pipeline and the business to get medicines to patients as efficiently and optimally as possible. The Regulatory Affairs Director (RAD) provides strategic and operational regulatory leadership to the development commercialization and life cycle management of assigned oncology products. Serves as the global regulatory lead (GRL) on early stage projects or specific indications of larger programs and/or as the regional regulatory lead. The RAD plays a substantial role crafting and implementing the clinical strategy and influencing health authorities to improve outcomes. Cambridge UK is one of over 400 sites here at AstraZeneca providing a collaborative and vibrant environment where everyone feels comfortable and able to be themselves is at the core of AstraZenecas priorities. * Lead cross functional teams in major regulatory submissions (NDA/BLA/IND/CTA) health authority interactions label discussions and securing approvals. * Develop and implement the programs regional or global strategy ensuring that it is crafted to deliver rapid approval with competitive labeling that is identified by the business markets and patients. * Craft the health authority engagement strategy and interaction plan drive the formulation of the briefing document focused on strategy and scientific content lead the team through meeting rehearsals and moderate the meeting itself. * Lead a Global Regulatory Strategy Team (GRST) of key contributing members from the regions emerging markets RA CMC Labeling and members of the submission and execution team. Mentor and provide performance feedback to members of your GRST. * Deliver regulatory milestones on your team including an assessment of risks and mitigations emerging data and the probability of success. Lead preparation of the regulatory strategy document and target product labeling. * Own the negotiations with health authorities and initiate and deliver key regulatory documents. * Plan and construct the global dossier and core prescribing information including product maintenance supply and compliance activities. * Partner with marketing companies (countries) and regional regulatory affairs staff to influence developing views/guidance. * Bachelors degree in a science related field with at least 3 years of Regulatory strategy or related knowledge/experience. * A solid knowledge of regulatory affairs within at least one therapeutic area in both early and late development. * Previous demonstrated experience of regulatory drug development or equivalent and experience with major HA interactions. * Demonstrated competencies of strategic thinking strategic influencing risk evaluation innovation initiative leadership and excellent oral and written communication skills. * Advanced degree preferred. * Experience in Oncology (small molecules & biologics) is preferred. * Prior experience with phase 3 design including end of phase 2 health authority interactions. * Contribution to a regulatory approval including leading response team and labeling negotiations. * Knowledge and understanding of guiding principles in drug development such as benefit/risk profile dose selection or statistical design. * Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs. * Ability to work strategically within a business critical and high-profile development program. * Critical thinking on current global regulatory science questions and good understanding of the corresponding scientific and clinical component. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills. We believe that the more inclusive we are the better our work will be. We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics. We follow all applicable laws and regulations on non-discrimination in employment (and recruitment) as well as work authorization and employment eligibility verification requirements. Competitive salary and benefits package on offer: Recognizing the importance of individualized flexibility our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Date Posted 17-Oct-2025 Closing Date 29-Nov-2025 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion starting with our recruitment process. We welcome and consider applications from all qualified candidates regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations please complete the section in the application form. Required Experience: Director Key Skills Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills Employment Type : Full-Time Experience: years Vacancy: 1

We seek a Communication Lead in our UK/Ireland Business Area to drive marketing and customer engagement initiatives through data-driven 2-year strategies. The role involves product branding content creation across platforms and managing integrated campaigns with multiple teams. Key responsibilities include developing targeted customer communications managing budgets and KPIs analyzing performance metrics and building material for digital touchpoints. The ideal candidate will combine strategic planning with creative content development to strengthen brand loyalty and drive business growth. Responsibilities/accountabilities will also include: • Create content to engage customers and develop excitement to drive product sales and loyalty., • Develop and execute data-driven communication strategies for crop segments aligning business priorities with customer needs while ensuring personalized engagement across all touchpoints to deliver measurable results., • Ensure campaigns adhere to marketing budgets optimizing value for money within budget boundaries., • Ensure an effective media plan balancing in-house and external resources for efficient campaign delivery., • Work closely with Crop Portfolio Solutions Managers to ensure campaigns align with portfolio strategy., • Facilitate successful Campaigns including new product introductions creating communication plans and tracking campaign performance by setting relevant leading and lagging KPIs investigating and implementing new marketing communication techniques in response to a changing market., • Bachelors degree or equivalent in Agriculture Business or related fields such as Marketing/Communications., • Solid background in marketing ideally in Communications or Operations for complex markets in cross-cultural environments. Experience and good working knowledge of digital marketing is desired., • Strong interest in agricultural or the willingness to learn is essential., • Strong expertise in Marketing Data Science CRM systems and digital marketing across multiple platforms with proven ability to analyze metrics and ensure regulatory compliance., • A portfolio of content development and strategic communications to varied audiences., • Proven ability to coordinate with cross-functional teams and execute strategic communications across diverse stakeholders while maintaining a customer-centric focus. Additional Information : Syngentas site at Cambridge is the location for the commercial operations of Syngentas Crop Protection Seeds Flowers and Lawn & Garden businesses in the UK and Ireland. Activities include sales marketing technical support customer support HR Finance and administration functions. What we offer • Extensive benefits package including a generous pension scheme bonus scheme private medical & life insurance., • Flexible working ideally 2-3 office days per week., • Up to 31.5 days annual holiday., • We offer a position which contributes to valuable and impactful work in a stimulating and international environment., • Learning culture and wide range of training options. Remote Work : No Employment Type : Full-time Key Skills Administrative Skills,Facilities Management,Biotechnology,Creative Production,Design And Estimation,Architecture Experience: years Vacancy: 1

The Senior Manager Regulatory Affairs CMC will be responsible for the development execution and tracking of CMC regulatory activities for assigned BicycleTx programs or projects. You will be responsible for supporting the development of CMC regulatory strategy and processes for their assigned BicycleTx programs or projects working closely with cross-functional colleagues and the Director Regulatory Affairs CMC. As an integral member of the team that will be tasked with CMC product development the Senior Manager Regulatory Affairs CMC will also serve as a subject matter expert (SME) for assigned activities which may involve multiple partners and collaborators and will ensure adherence to relevant regulatory requirements. Key Responsibilities • Responsible for the development and execution of regulatory strategy and submissions for assigned BicycleTx programs or projects with a focus on regulatory CMC including dossiers to support clinical trial applications, • Responsible for the regulatory assessment of change controls maintenance of regulatory files and tracking databases related to CMC submissions, • Collaborate with internal colleagues and external organizations to develop submission content plans and timelines and support the timely execution of regulatory submissions that require CMC content responses to questions audits and inspections, • Manage the preparation drafting review risk analysis and mitigation planning of CMC submissions (e.g. Module 3 IND IMPD amendments and annual reports) for assigned BicycleTx programs or projects, • Developing and maintaining internal cross-functional relationships to support the development and execution of CMC regulatory submissions for assigned BicycleTx programs or projects, • May act as the Global/Regional CMC Regulatory Lead for assigned development programs, • May support the development of processes SOPs and other controlled documents including for Regulatory Affairs activities, • Partners with Regulatory Affairs and cross-functional colleagues to understand the CMC regulatory landscape e.g. views of HAs regulatory precedents labeling differences and other CMC-specific issues and adapts to changes that may impact BicycleTx programs or projects We are also open to those that can commit to a minimum of 0.8FTE (4 day week) We are only considering candidates who have a mix of CMC and Clinical Regulatory Affairs experience. Qualifications : Key Skills and Competencies • Bachelors degree in a scientific field or post-graduate degree preferred, • Strong demonstrable experience in CMC Regulatory Affairs within the pharmaceutical or biotechnology industry; particularly relating to peptides and drug-conjugates; any in-depth experience may be limited to one specific region (e.g. US or EU)., • General clinical regulatory experience supporting global clinical trial applications (not limited to CMC) is essential., • Working knowledge of FDA EMA ICH and cGMP CMC regulatory guidance and regulations, • Experience and knowledge in preparation of CMC sections of INDs CTAs NDAs MAAs or regional equivalents is required, • Experience and knowledge in the supportive interactions with health authorities including US FDA EMA and/or EU Member States is desirable, • An understanding of the drug product lifecycle from discovery to clinical trials to marketing is required, • Ability to communicate on topics of basic science is essential; a working knowledge of global drug product development is required, • Ability to proactively identify risks and develop risk mitigation strategies, • Adaptable with the ability to generate creative solutions identify different and novel ways to find solutions and adapt to changing priorities and deadlines., • Highly collaborative strong relationship building skills with internal and external partners with a high level of integrity, • Works proactively using solid communication and influencing skills to effectively execute program goals for assigned BicycleTx programs or projects, • Works effectively in a highly complex and fast-paced environment, • Strong organisational and time management skills, • Position may require some domestic and international travel Additional Information : • State-of-the-art campus environment, • Competitive reward including annual company bonus, • 28 days annual leave in addition to bank holidays, • Employer contribution to pension (employee does not have to contribute), • Life assurance cover 4x basic salary, • Private Medical Insurance including optical and dental cover, • Health Cash Plan, • Eligibility for an option grant to subscribe to shares in Bicycle Therapeutics plc. Remote Work : No Employment Type : Full-time Key Skills Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills Experience: years Vacancy: 1

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference. Every member of Gileads team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future you are the key driver in evolving our culture and creating an environment where every employee feels included developed and empowered to fulfil their aspirations. Join Gilead and help create possible together. Job Description FUNCTION: Global Therapeutic Area (TA) Regulatory Liaisons POSITION OVERVIEW: We are looking for a unique individual who is passionate about advancing therapeutics and thrives under pressure. This is an exciting opportunity for a Senior Manager to join the Gilead Virology Team. The future of the role encompasses providing regulatory strategy leadership and support as the Regional Regulatory Lead on the assigned products compounds indications or projects. With guidance defines the regulatory strategy plans and objectives for the assigned products or projects. You will lead the Regulatory Submissions Teams associated with assigned products or projects and represent Global TA Regulatory to cross-functional sub-teams. May serve as a Gilead contact to / for regulatory authorities. Manage oversee and coach less experienced colleagues. You will oversee and manage the work of less experienced colleagues supporting your work. You will coach and advise less experienced colleagues in completing their work and developing their regulatory capabilities. Typically assigned products compounds indications or projects of increasing complexity. May play a more active role in process improvements and other special projects that can carry significant value to multiple Regulatory Affairs activities and teams. JOB RESPONSIBILITIES: • Represents regional Regulatory Affairs or may serve as Regional Lead on cross-functional teams ( e.g. Study Management Clinical Nonclinical Biomarkers and/or cross-regional Regulatory Submission Teams., • With guidance defines the regulatory strategy for one or more Gilead products or projects (development or marketed products)., • Proactively identifies regulatory or related risks/issues and develops mitigation and/or contingency plans., • Leads the preparation compilation and timely filing of complex regulatory submissions which require cross-functional interactions for commercial or investigational product(s) for assigned territories in line with ICH requirements regional requirements and scientific and company policies and procedures. Examples include meeting requests briefing packages initial clinical trial applications/Amendments or routine submissions (e.g. Development Safety Update Reports / DSURs Investigator Brochure/ IB updates etc.) as well as post-approval submissions for marketed products., • Leads cross-functional teams in the authoring of regulatory documents and including meeting requests., • Responsible for ensuring regional product labelling is created and maintained in alignment with the Company Core Data Sheets (CCDS) and Company Core Safety Information (CCSI)., • Ensures product packaging and associated information is updated and maintained in accordance with the product license for assigned products and markets., • Critically reviews documents for submission to regulatory authorities., • Initiates or otherwise contributes to process improvements and/or other special projects within Regulatory Affairs., • Ensures own work complies with established practices policies and processes and any regulatory or other requirements. Education and/or Experience required • Life Science degree, • Extensive experience Regulatory Affairs or other relevant industry experience, • Experience setting the regulatory strategy and leading regulatory submissions and other activities for a medicinal product is strongly preferred., • In-depth knowledge of regulatory requirements including ICH requirements and regional requirements for assigned territories and have an in-depth understanding of current global and regional trends in Regulatory Affairs., • Good knowledge of regulatory requirements for the EU centralised procedure. Experience in co-ordinating post-approval variations renewals responses to questions PSURs etc. for EU centralised products is desirable., • Experience of regulatory requirements in other countries/regions is desirable., • Experience in clinical trials applications/amendments in the European Union and good breadth of understanding of European regulations relating to clinical trials would be advantageous., • Experience in working with document management systems., • Experience successfully leading departmental and cross-functional teams without authority., • Experience authoring and implementing processes., • Experience working with one or more Gilead therapeutic areas and varying stages of drug development is strongly preferred. Knowledge & Other Requirements • Excellent verbal and written communication skills and interpersonal skills are required., • Demonstrated ability to be a fast learner., • Demonstrated ability to be flexible and adaptable to change to move between projects easily and provide support/expertise where needed., • Demonstrates advanced knowledge of regulatory requirements and the role of regulatory affairs in achieving cross-functional drug discovery and development goals and objectives including ICH standards and the regulatory requirements for assigned markets., • In-depth knowledge of relevant health authorities including people system processes and requirements as evidenced by past effectiveness and successes in conducting HA interactions., • Able to represent Gilead to regulatory authorities when managing standard or more routine negotiations., • Demonstrates strong analytical thinking skills attention-to-detail strong communication and writing skills project management skills and proficiencies with Microsoft Office suite as evidenced through accomplishments in past roles., • Ability to lead and influence programs projects and/or initiatives., • Strong interpersonal skills and understanding of team dynamics., • Proven ability to work successfully in a team-oriented highly-matrixed environment., • When needed ability to travel. It is the policy of Gilead Sciences Inc. and its subsidiaries and affiliates (collectively Gilead or the Company) to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law all employment actions relating to issues such as compensation benefits transfers layoffs returns from layoffs company-sponsored training education assistance social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds which may include an individuals gender race color national origin ancestry religion creed physical or mental disability marital status sexual orientation medical condition veteran status and age unless such protection is prohibited by federal state municipal provincial local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws. Please apply via the Internal Career Opportunities portal in Workday. Required Experience: Manager Key Skills Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills Employment Type : Full-Time Experience: years Vacancy: 1

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference. Every member of Gileads team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future you are the key driver in evolving our culture and creating an environment where every employee feels included developed and empowered to fulfil their aspirations. Join Gilead and help create possible together. Job Description This exciting role of Regulatory Affairs Associate II CMC sits in Gileads CMC Regulatory Affairs - Small Molecule Group. Responsibilities and qualifications are as follows: Responsibilities: * Provides support for designated regional regulatory activities for PDM CMC Project and Commercial Teams Regulatory Project and Regulatory Submissions Teams with focus on Small/Synthetic Molecules. * Assists designated CMC RA leads in identifying and ranking risks proposing risk mitigation plans. Shadows leads while they develop and execute robust CMC regulatory strategies. * Under the guidance of more senior staff oversees the preparation of CMC regulatory submissions for investigational and commercial products with solid scientific foundations in compliance with ICH and regional requirements and in alignment with company policies and procedures. * Will become proficient in utilizing computerizing systems as per established business processes both within and outside of the GxP environment. * Will train and learn how to prepare regulatory submissions which require some interactions with other members in the CMC regulatory department for investigational and commercial products in line with ICH requirements regional requirements and scientific and company policies and procedures. * Will perform workflows and procedures regarding document tracking indexing and retrieving and disseminating information to the CMC regulatory department. * Participates in group meetings and provides tactical approaches to addressing issues of low to moderate complexity. * May participate in other Subteams and in non-product related projects; may contribute to local process improvements which have an impact on the working of the CMC Regulatory function or other departments. * Learns how to interpret regulatory guidelines and how to comply with statutory requirements. * Learns how to provide regulatory impact assessments for changes managed in the quality systems and participates in technical risk assessment exercises. * Proactively invests in own development to acquire regulatory skills and knowledge with manager support. * Invests in acquiring knowledge about CMC regulatory intelligence including guidelines and regulatory trends. Basic Qualifications: * Ph.D. Masters or pharmacy chemistry or related field with experience working in scientific/technical group within a pharma company Preferred Qualifications: * Experience with small molecule/synthetic pharmaceuticals would be preferred * Collaborative proactive and highly organized approach to work. * Demonstrated track record with strategic planning problem solving and working within a global matrix team environment. * Good understanding of the drug development process. * Excellent verbal and written communication skills and ability to interact well with colleagues and stakeholders * Experience in a GMP environment is preferred * Ability to learn on the job is preferred It is the policy of Gilead Sciences Inc. and its subsidiaries and affiliates (collectively Gilead or the Company) to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law all employment actions relating to issues such as compensation benefits transfers layoffs returns from layoffs company-sponsored training education assistance social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds which may include an individuals gender race color national origin ancestry religion creed physical or mental disability marital status sexual orientation medical condition veteran status and age unless such protection is prohibited by federal state municipal provincial local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws. Please apply via the Internal Career Opportunities portal in Workday. Key Skills Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills Employment Type : Full-Time Experience: years Vacancy: 1

What Youll Do Install, exchange and commission smart gas and electric meters Complete diagnostics, safety checks and remedials Deliver excellent customer service and clear explanations to households Ensure regulatory compliance and accurate job closure using a handheld device Contribute to nat

Your new company A well established, privately owned UK construction company operating throughout the UK. They deliver major projects across a number of sectors including education, leisure, commercial, and industrial. They have a strong focus on sustainability, community engagement and social value. Your new role An opportunity has arisen for a Design Manager to join the construction team based in the Cambridge area. The role involves overseeing design development from early consultation through to live project delivery, ensuring alignment with project intent and compliance standards. As Design Manager, you will bring strong leadership skills, experience in a principal contracting environment, and a collaborative approach to stakeholder engagement. Duties include: Leading design coordination across projects Managing consultants and subcontractor design inputs Overseeing design programmes, RFIs, and document control Ensuring regulatory compliance and planning conditions are met Promoting buildability and safety in design Supporting BIM processes and digital model reviews Contributing to pre-construction and value engineering efforts Maintaining technical and commercial awareness Representing the design function in client meetings Sharing lessons learned and mentoring junior team members What you'll need to succeed Demonstrated success in a design coordination or management role, preferably within a principal contractor setting. Strong technical foundation, supported by a degree or equivalent qualification in a construction-related field. Comprehensive knowledge of current legislation, including the Building Safety Act, CDM regulations, and Building Regulations. Proven ability to lead multidisciplinary teams and oversee specialist subcontractor activities. Highly organised, proactive, and an effective communicator. Comfortable managing diverse project types, tight timelines, and intricate design challenges. Prior experience working on Department for Education frameworks is preferred. 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, or call us now. 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 EA is a trading division of Hays Specialist Recruitment Limited and 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 TPBN1_UKTJ

Web Designer & Web Developer Near Cambridge My client, a fast-growing AI company based near Cambridge, is seeking a talented Web Designer & Web Developer to design, build, and maintain the organisations websites and digital content. This role blends creative design, front-end development, and digital content production-ideal for a recent graduate or early-career designer with a strong visual portfolio and solid technical web skills. You will work closely with the marketing and creative teams to shape the companys digital presence, deliver high-quality visual assets, manage multiple web projects, and ensure all online platforms remain modern, engaging, and technically robust. Key ResponsibilitiesWeb Design & Front-End Development Designing and building website pages, templates, and components using HTML, CSS, and modern web standards Managing and updating company websites via CMS platforms (WordPress, Joomla, or similar) Creating wireframes, mock-ups, and page layouts incorporating fonts, colour schemes, imagery, animations, and interactive elements Ensuring usability, responsiveness, accessibility, and smooth user navigation Editing, debugging, and improving existing pages and site structures Implementing SEO best practices and monitoring site performance through analytics Digital Content & Creative Production Producing digital artwork, graphics, and visual assets using Adobe Creative Cloud (Photoshop, Illustrator, InDesign) Supporting creation of 3D and motion content (experience with Blender is an advantage) Creating and editing video and podcast content for marketing and communications Retouching images, developing visualisations, and delivering brand-consistent assets Ensuring branding guidelines are consistently maintained across all digital outputs Website Operations & Management Registering domains and coordinating hosting and DNS updates with internal IT Managing website testing, quality checks, and daily performance evaluations Ensuring compliance with accessibility, privacy, and other digital regulatory requirements Tracking traffic and user engagement through analytics tools and producing insights Keeping up to date with modern web design trends, technologies, and best practices Cross-Team Collaboration Working with internal teams to plan social media assets, video content, and marketing campaigns Liaising with external agencies, photographers, creative partners, and printers Supporting the 3D designer and other creative roles as needed RequirementsEssential Proficiency in HTML, CSS, and at least one major CMS (WordPress, Joomla, etc.) Strong graphic design skills, particularly within Adobe Creative Cloud (Photoshop, Illustrator, InDesign) Ability to produce high-quality digital artwork and retouched imagery Excellent time management and organisational skills, with the ability to manage multiple projects Strong communication skills and the ability to work independently within a small team Full UK driving licence Full eligibility to work in the UK (no sponsorship available) Desirable Experience with Blender or other 3D creation tools Video editing or podcast production experience Knowledge of desktop publishing (DTP) software Familiarity with accessibility standards and GDPR/privacy requirements Understanding of SEO, analytics tools, and performance optimisation Basic understanding of JavaScript or front-end frameworks Role Details Location: near Cambridge Working Pattern: Office-based, 5 days per week Team: Creative, technically varied role within a small and expanding marketing team Opportunity: Shape the companys entire digital presence in a high-growth tech environment Interested? Please Click Apply Now!Web Designer & Web Developer Near Cambridge TPBN1_UKTJ

You’ll also play a key role in ensuring compliance with regulatory frameworks, including UK charity regulations and GDPR, while embedding digital transformation in support of Fauna & Flora’s vital work protecting nature around the world. In return we offer the opportunity to work for a ground-br

Serve as the go to contact for internal RA CMC queries from the technical and quality team, including due diligence and regulatory agency interactions, to resolve issues efficiently and support informed decision making* Ensure all regulatory processes, controlled documents, and knowledge resources a

Continuously develop best practices for the Clinical Regulatory Writing organization. Represent Clinical Regulatory Writing on various improvement workstreams and external activities. Proficiency at authoring/editing and managing the writing/review of multiple types of clinical regulatory documents

Provide practical advice on data protection (UK GDPR, Data Protection Act 2018), privacy notices, and data processing arrangements. Flexible working model – remote or hybrid options available. Provide legal guidance on UK and EU regulatory frameworks, including FCA regulations, PSD2, e-money, AML.

Strong governance, risk, and compliance capabilities within charity or non-profit sectors preferred. You’ll also play a key role in ensuring compliance with regulatory frameworks, including UK charity regulations and GDPR, while embedding digital transformation in support of Fauna & Flora’s vita

Regulatory investigations and environmental defence.

A leading global biopharmaceutical company in Cambridge is looking for a Director of Clinical Regulatory Writing.

Job Title: Business Operations Support Manager Salary: £29,700 - £38,550 Location: Cambridge, Hybrid (at least 2 days per week in the office) Contract: Permanent, Full time (35 hours per week) We are looking for a Business Operations Support Manager to join our English Product Group and help us deliver excellence. In this role, you will collaborate with our Quality and Risk Managers to ensure key areas of our business operate within a robust Quality Management System and also that we are effectively managing risks and business continuity. Your work will enable us to remain resilient and deliver products and services that meet customer and regulatory requirements, foster customer satisfaction, and drive continuous improvement. We are Cambridge University...

Are you an experienced PLM Manager (Product Lifecycle) with a strong background in engineering, manufacturing, or product lifecycle control? This is an excellent opportunity to join a well-established organisation specialising in advanced safety and detection technologies. Responsibilities of the PLM Manager (Product Lifecycle) job based in Cambridge: Define, implement, and maintain configuration management processes, standards, and best practices. Ensure accurate creation and maintenance of product structures, variants, and associated documentation. Control and monitor configuration changes throughout the product lifecycle, ensuring complete traceability. Collaborate with engineering, production, compliance, and commercial teams to align configuration data with operational needs. Support product certification and regulatory compliance through accurate configuration records. Provide training, coaching, and guidance to stakeholders on configuration procedures and PLM methodologies. Support the implementation of a new PLM (PDM) system, transitioning existing manual processes into improved digital workflows. Manage and ensure timely approval of Engineering Change Notices (ECNs) across the organisation. Skills & experience required of the PLM Manager (Product Lifecycle) job based in Cambridge: Proven experience in configuration management or a closely related engineering/manufacturing discipline. Hands-on experience with PLM upgrades/implementations and robust change control processes. Strong ability to interpret technical documentation, drawings, and product specifications. Proficiency with PLM/configuration management tools and ERP systems. Knowledge of modern industry best practices for configuration control and lifecycle management. Experience leading, coaching, or developing team members to improve engineering capabilities. Degree (or equivalent) in engineering, manufacturing, or a related field. Benefits for the PLM Manager (Product Lifecycle) job based in Cambridge: Pension up to 10.5% Bonus Private healthcare If this PLM Manager (Product Lifecycle) job based in Cambridge could be of interest, send your CV to or call Ben on 01582 878816 / 07471 181784. TPBN1_UKTJ

Strong understanding of service delivery models and project management methodologies (Agile, PRINCE2, ITIL, etc. The role ensures initiatives align with the organisation’s business goals and regulatory requirements, and oversees service delivery and operational readiness of new systems and technol

As the Senior Regulatory Affairs Director you will be accountable for leading the development and implementation of the global regulatory strategy for a product/group of products of increasing complexity. Expert knowledge of regulatory affairs within one or more therapeutic areas. Broad background o

Liberty Global is an equal opportunity employer. The Analyst will play a key role in collaborating with the business which includes colleagues in LAC, M&A, Strategy, Content, and other key teams within Liberty Global, as well as the management and the legal teams of our operating companies and i

The Regulatory Affairs (RA) Associate in the Global RA Coordination team is responsible for managing the Global RA inbox, coding invoices, reporting sales figures, archiving, and providing general support to the RA group.

You will act as a regional regulatory lead, guiding cross-functional teams and serving as a key contact for regulatory authorities. Are you ready to lead complex regulatory submissions and influence cross-functional teams?. Position: Senior Manager, Global Regulatory Affairs.

Regulatory Compliance Manager – Betting & Gaming. As a visible and trusted advisor, you’ll balance regulatory integrity with commercial ambition, ensuring the business continues to deliver innovative, customer-focused betting experiences while supporting the wider racing industry.