Offres pharmaceutical industry à CambridgeCréer des alertes d'emploi

Mantell Associates is partnered with a rapidly expanding AI‑powered small molecule drug discovery CRO based in Cambridge, who is seeking a Business Development Director to lead and scale commercial growth globally. This is a rare opportunity to shape the go‑to‑market strategy for a platform that combines cutting‑edge machine learning with deep chemistry expertise to accelerate discovery for biotech and pharmaceutical partners. Business Development Director - Responsibilities: • Developing and executing the commercial strategy to achieve ambitious growth targets, • Identifying, qualifying, and closing new business opportunities across biotech, pharma, and research organisations, • Building and nurturing long‑term relationships with senior scientific and commercial stakeholders, • Clearly articulating the value proposition of the company’s AI‑enabled discovery services, • Collaborating with internal scientific, delivery, and leadership teams to support proposal development and contract negotiation, • Attending and representing the company at key scientific and industry conferences Business Development Director - Requirements: • Significant experience (typically 10+ years) in business development, sales or commercial leadership within life sciences, drug discovery services, CROs, or technology platforms, • A strong track record of selling scientific services or technology into biotech and pharmaceutical organisations, • Commercial acumen with the ability to manage complex sales cycles and close high‑value deals, • Excellent communication skills, with the ability to engage and influence senior decision‑makers, • A scientific understanding of early drug discovery, computational platforms, or AI/ML technologies (preferred but not essential), • An entrepreneurial mindset, proactive approach, and a desire to build and scale commercial functions Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at +44 (0)20 3854 7700.

Patient Support Programme (PSP) Manager UK & Ireland | Hybrid (Cambridge area – 1 day per week) Competitive salary circa £90,000 + bonus + benefits Opportunity to take full ownership of Patient Support Programmes across the UK & Ireland within a global rare disease organisation, combining governance leadership with operational delivery. A global biopharmaceutical company focused on rare diseases is seeking a Patient Support Programme (PSP) Manager to oversee the governance, performance and operational management of patient support and homecare services across the UK and Ireland. This role sits within the Medical Governance function and plays a critical part in ensuring PSPs deliver real value for patients, healthcare providers and the wider healthcare system while maintaining the highest standards of compliance. You will act as the PSP Owner, leading programme governance, vendor oversight and operational performance while working closely with Medical, Compliance, Market Access, Commercial teams and external healthcare partners. Key responsibilities • Own the governance and lifecycle management of Patient Support Programmes across the UK & Ireland, • Lead cross-functional PSP governance reviews and ensure compliance with regulatory and internal frameworks, • Manage relationships with homecare providers and external service partners, ensuring high-quality service delivery, • Oversee contracts, KPIs and operational performance across PSP providers, • Analyse programme data to identify insights, risks and opportunities to improve patient outcomes Candidate profile We are looking for someone with experience in Patient Support Programmes, homecare services, or healthcare operations within the pharmaceutical or biotech industry. You will bring: • Strong understanding of governance frameworks, regulatory expectations and compliance requirements associated with PSPs, • Experience managing vendors, service providers and contractual relationships, • Strong analytical capability and confidence interpreting operational and performance data, • Excellent organisational and project management skills, • Ability to work cross-functionally with Medical, Compliance, Market Access and Commercial teams, • Degree in life sciences, pharmacy, nursing, medicine or a related discipline, • Experience in rare diseases or speciality therapeutic areas would be advantageous. Additional information • Hybrid role with weekly presence in the Cambridge area, • UK & Ireland travel required for provider meetings and service reviews, • Opportunity to play a key role in shaping patient support services that improve real-world patient outcomes For a confidential discussion, please contact me directly via LinkedIn or click "Apply" below

We are currently looking for an Analytical Chemist for a company in Cambridgeshire. As an Analytical Chemist, you will conduct a range of analytical testing in support of R&D and manufacturing. Responsibilities include: • Run various chemical analysis using HPLC, GC and FTIR., • Carry out analytical method development and validation., • Troubleshooting analytical methods and instrumentation., • Write and review documentation for the laboratory., • Ensure all laboratory analysis is compliant and according to the relevant quality standards. Ideal candidates will have: A degree/ Masters (MChem, MSc, MSci) in Chemistry or Analytical Chemistry and have experience in HPLC and GC analysis within industry. Some experience in HPLC or GC method development and/ or method validation is desirable. To apply for the Analytical Chemist role please send your CV to Peter at Rowland Talent Solutions. Please note candidates need to have the right to work in the UK. Key words: Chemistry, QC, Analyst, Analytical Chemist, GC, Pharmaceutical, Chemical, HPLC, GC, Quality Control

We are currently looking for a Device Industrialisation Engineer to join a leading Pharmaceutical company based in Cambridgeshire. As a Device Industrialisation Engineer, you will be instrumental in contributing to medical device and combination product projects. This is an initial 12 month contract and is a hybrid position (50% onsite). KEY DUTIES AND RESPONSIBILITIES: Your duties as the Device Industrialisation Engineer will be varied however the key duties and responsibilities are as follows: 1. As the Device Industrialisation Engineer, you will deliver key industrialisation activities on medical device and combination product projects within complex generics and biosimilar workstreams., 2. As the Device Industrialisation Engineer, you will provide expertise and input into device scale-up activities, including DFM, DFA, precision component moulding, and assembly., 3. As the Device Industrialisation Engineer, you will manage tech/design transfer activities for medical/pharma products moving from R&D into production., 4. As the Device Industrialisation Engineer, you will input into and write manufacturing-related sections of DHF documentation, manage suppliers, and oversee capital equipment acquisition. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Device Industrialisation Engineer, we are looking to identify the following on your profile and past history: 1. Relevant degree in mechanical, chemical, or process engineering, pharmaceutical sciences, life sciences, or other relevant subjects., 2. Extensive industry experience in the development of medical devices and/or combination products within a pharmaceutical, medical devices, and/or combination products setting., 3. A working knowledge and practical experience with process development tools, industry-accepted risk management, and validation methods. Key Words: medical device / combination product / industrialisation / generics / biosimilars / tech transfer / process development / DFM / DFA / precision moulding / supplier management Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

PAT TESTER Considering making an application for this job Check all the details in this job description, and then click on Apply. Full time - Monday to Friday COMPANY OVERVIEW Our client is one of the UK's leading providers of electrical safety services, specifically inspection and testing of fixed installations. Demand for their Electrical Equipment Testing (EET) (Formerly PATs) services is high, so they are continually looking to expand our national team of Engineers. COMPANY USP'S Collectively 120 years management experience in advising on ‘Safe Places at work, Safe Systems at work & Safe People at work' Industry Authority - authors of practical guidance to assist Duty Holders on meeting the demands of EaWR1989 Technological Pioneers - Development of on-site & on-line technology to enable immediate client access & update of records, regardless of location Inspection & testing work carried out in pairs 93% client retention Blue Chip Client base - Industrial, Manufacturing, Pharmaceutical, Healthcare, Aerospace, Food & Drink, Sports & Leisure, Education. No High St retail or domestic JOB PURPOSE The role will require you to safely carry out inspection and testing of electrical equipment and produce results/reports that meet the requirements of the current edition of the IET Code of Practice, clients, and external accrediting bodies in the Glasgow area. xrnqpay JOB SPECIFICATION Carry out In-service Inspection and Testing of Electrical Equipment (EET) in accordance with the current edition of the IET Code of Practice Produce results which meet the requirements and quality standards of clients and external accrediting bodies Adhere to Company Health & Safety Policies and Procedures at all times Act with integrity and professionalism in all communications with clients and colleagues Keep abreast of changes and amendments to standards, regulations and best practices within the industry QUALIFICATIONS / EXPERIENCE City & Guilds 2377 Full UK Driving Licence Relevant computer literacy to enable generation and electronic submission of results Strong verbal communication skills Basic numeracy and literacy skills Flexibility and good personal organisation SALARY/BENEFITS £29,535 £35k to £40k OTE 30 paid holidays plus including B/H's (8 Days) Company Van Paid 12 hours for each day staying away Hotel and food allowance provided when staying away If you are interested please call Tom on or please apply to this advert to prompt a call back!

Knowledge of the Pharmaceutical Bioscience and Diagnostic industry an advantage.

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Associate Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals’ Pharmaceutical Development programs at various stages of the development life-cycle including preformulation, formulation and process development, technical transfer and validation. The Associate Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre-formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Associate Director of Drug Product Development may provide leadership of cross-functional CMC development teams. The Associate Director of Drug Product Development will have broad experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills. Essential Functions Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing. Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial); and in developing robust processes for pharmaceutical production. Directs projects and leads cross-functional teams (as required) with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget. Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs). Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors. Work cooperatively with, or lead, internal and external teams as required. Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators. Supports asset due diligence and new product introduction and integrations Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations. Required Knowledge, Skills, and Abilities 10 years’ experience in drug product development in the pharmaceutical industry required. Direct experience with formulation development, process development, technical transfer and/or process validation. Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong teamwork skills. Demonstrated troubleshooting and problem-solving skills including the use of designed experiments, statistical process control, Development/authorship of CMC regulatory filings for pharmaceutical products. Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms preferred. Excellent written and verbal communication skills Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation. Experience in intellectual property development desirable. Proven project management skills for technical programs. Flexibility to travel on company business when required Required/Preferred Education and Licenses Advanced degree in Chemistry, Pharm. Sci., Engineering, or related field, or equivalent combination of education and work-related experience required. Description of Physical Demands Occasional mobility within office environment. Routinely sitting for extended periods of time. Constantly operating a computer, printer, telephone and other similar office machinery. 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: $(phone number removed) - $(phone number removed) 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

Are you a master of logic, flow, and precision? This pharmaceutical company is seeking a high-impact leader to take the helm of their site operations on the outskirts of Cambridge. This isn't just about moving boxes; it is a critical leadership role responsible for the entire lifecycle of the manufacturing workflow, from the moment raw materials hit the dock to the final distribution of these life-changing products. What's your mission: You will be the "air traffic controller" of the site. Your goal is to ensure that production processes are lean, this highly regulated warehouse is compliant, and that manufacturing schedules are met with surgical precision. Salary circa £60,000 depending on the skills and experience you are bringing to the table - along with excellent benefits including private healthcare and dental cover, generous holiday allowance, life assurance cover and share scheme. What you will be doing: * Develop and execute detailed production schedules and capacity plans that optimise the use of resources and materials. * Oversee daily operations (receiving, storage, shipping) while ensuring strict adherence to GMP and GDP standards. * Implement lean processes, systems and monitor stock levels to ensure the company will never face a stockout or a bottleneck. * Lead and coordinate with teams across Manufacturing, QC, R&D, and Procurement to keep business goals aligned. * Proactively identify potential supply chain disruptions or equipment downtime and build the contingency plans that keep things moving. What you need: * You are a problem-solver who thrives under pressure and can communicate complex plans to everyone from shop floor to senior management. * Extensive experience in production planning or scheduling, preferably within the pharmaceutical industry or other heavily regulated industry if not. * A degree level qualification or equivalent, in Operations Management or other relevant subject. * Knowledge of GMP/GDP systems and pharmaceutical regulations (ICH guidelines). * Proficient in ERP planning software (SAP, Oracle, or equivalent) and the Microsoft Office suite (especially Excel). * Experience with Kanban, Six Sigma, or other quality management methodologies is a major plus. You will have full accountability for optimising production workflows, right through to despatch. If you'd be up for this challenge, in a highly regulated, fast-paced environment, then apply today

Pharmaceutical Operations Associate Location: Toft, Cambridge (relocating to Melbourn) Salary: £25,000 – £26,000 per annum Type: Full-time, Permanent (on-site) The Company Our client is a growing pharmaceutical wholesaler, supplying specialist medicines and healthcare products to a wide range of customers. Operating within a highly regulated environment, they pride themselves on accuracy, reliability and excellent customer service. As a small, close-knit team, they offer a hands-on environment where individuals can make a real impact and develop their skills quickly. The Role This is a varied and practical operations role supporting the day-to-day running of the business across customer service, administration and warehouse activities. You will play a key part in ensuring orders are processed accurately, customers are supported effectively and operations run smoothly in line with strict pharmaceutical regulations. This role would suit someone who is detail-oriented, adaptable and keen to learn, rather than someone with extensive industry experience. Key Responsibilities * Accurately process customer orders and associated documentation * Handle customer enquiries and resolve queries in a professional manner * Liaise with suppliers regarding product availability and pricing * Monitor and track deliveries, ensuring timely fulfilment * Maintain accurate customer and order records using internal systems * Support pricing calculations and compare supplier options for specialist items * Assist with general administration including filing and document management * Provide support to warehouse operations, including: * Picking and packing orders * Stock checks and inventory control * Booking courier collections * Ensure all activities comply with Good Distribution Practice (GDP) regulations Skills & Experience * Strong attention to detail and high levels of accuracy * Confident using Microsoft Office (Word, Excel, Outlook) * Good numerical ability and commercial awareness * Excellent communication skills, both written and verbal * Previous experience in an administrative, customer service or operations role is beneficial * Experience with Sage or similar systems is advantageous but not essential Personal Attributes * Proactive and flexible with a “can-do” attitude * Comfortable working both independently and as part of a small team * Calm under pressure with the ability to manage a varied workload * Willingness to support different areas of the business as required * Keen to learn and develop within a growing organisation Additional Information * Full training will be provided, including regulatory compliance * A DBS check may be required * Driving licence desirable due to location This is an excellent opportunity to join a growing business in the pharmaceutical sector, offering genuine scope to develop your skills in a supportive, hands-on environment. Ideal for someone looking to build a long-term career within operations or healthcare. If you are interested in the role of Pharmaceutical Operations Associate and feel that you have the relevant experience, please contact your Recruitment Partner, Lisa Logan at Unicorn Resourcing. If this job isn't exactly right for you but you're looking for something new, please contact us for a confidential career discussion. Unicorn Resourcing Limited is acting as an Employment Agency in regard to this Permanent opportunity

Quality Lead Cambridge Up to £50k + 15% bonus Employee assistance program 10% Pension 33 days holiday Sickness pay HealthcareA well‑established manufacturer in the chemical sector is seeking a Quality Control (QC) Lead to oversee day‑to‑day laboratory operations. This role is ideal for an experienced analytical chemist who enjoys leading small teams, solving technical challenges, and ensuring high laboratory standards. Responsibilities Lead the daily workflow of the QC laboratory and support production priorities Carry out analytical testing using GC, HPLC, FTIR, KF, and titration techniques Review data, identify trends, and ensure accurate documentation in the ERP system Maintain and troubleshoot analytical instruments (GCs, HPLCs, gas generators etc.) Coordinate with external engineers for calibration and service work Write and update SOPs, work instructions, and other quality documentation Support audits, manage non‑conformances, and drive CAPA activity Mentor and develop QC Analysts while promoting a safety‑first culture Essential Degree in Chemistry/Analytical Chemistry, or relevant industry experience Strong hands‑on experience with GC, HPLC, FTIR, KF, titrations Understanding of method development and validation Experience working in a manufacturing or process‑driven environment Knowledge of COSHH and safe chemical handling Familiarity with ISO 9001 quality systems Confident communicator with strong organisational skills Proficient with Office 365 Desirable MSc or similar advanced qualification 5+ years' experience in a QC laboratory (chemical or pharmaceutical) Experience training or mentoring other analysts Strong record of troubleshooting complex analytical issues If you are interested in this position please click 'apply'. Hunter Selection Limited is a recruitment consultancy with offices UK wide, specialising in permanent & contract roles within Engineering & Manufacturing, IT & Digital, Science & Technology and Service & Sales sectors. Please note as we receive a high level of applications we can only respond to applicants whose skills & qualifications are suitable for this position. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business

About the opportunity Talent STEM is partnering with an innovative technology firm to find a Director of Business Development for their growing team in Cambridge. Our client is transforming how new molecules and materials are created, using cutting-edge technology to drive progress across pharmaceuticals and biotech. Backed by leading global investors, they are scaling rapidly and are looking for a commercial leader to drive growth. The role This is a key strategic position focused on expanding the company’s commercial footprint. You will identify and secure new business opportunities, build a high-value pipeline and establish long-term partnerships across pharma and biotech. A core part of this role will be leveraging your experience in small molecule drug discovery to engage with decision-makers and position the company’s offering effectively. You will represent the organisation at industry events, shape commercial strategy and work closely with senior leadership to convert opportunities into revenue. If you are a proactive deal-maker with a strong track record in small molecule discovery services or platforms, this is an opportunity to make a significant impact. What you’ll do Generate leads and achieve revenue targets by building and maintaining a strong pipeline. Align the company’s technology with market needs, focusing on high-value opportunities in small molecule drug discovery. Leverage your network to engage key stakeholders across pharma and biotech. Represent the company at conferences, trade shows and industry events. Manage proposals and negotiations through to contract completion. Collaborate with senior leadership to refine and execute the commercial strategy. What we need A degree in life sciences (MSc minimum). 6–7+ years of experience in senior business development or sales roles. Proven track record of securing high-value deals (multi-million-pound contracts). Strong experience in small molecule drug discovery services, platforms or CRO/CDMO environments. Established network within pharma and biotech. Excellent client-facing and relationship-building skills. Experience operating within the UK or European market. Bonus points MBA or advanced scientific/engineering qualification. Strong communication and collaboration skills. Commercially driven with a strategic mindset. Willingness to travel as required. Why this role? This is an opportunity to join a high-growth, well-funded organisation at the forefront of scientific innovation. You will have the autonomy to shape the commercial direction in a key market, supported by a leadership team with ambitious growth plans. How to apply Ready to take the lead? Apply now. Talent STEM is excited to connect you with this opportunity. Talent STEM is a specialist recruitment consultancy supporting the scientific, engineering, clinical, chemical, pharmaceutical, FMCG, environmental, biotechnology and medical device sectors

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals’ Pharmaceutical Development programs at various stages of the development life-cycle including preformulation, formulation and process development, technical transfer and validation. The Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre-formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Director of Drug Product Development will be expected to provide leadership of cross-functional CMC development teams. The Director of Drug Product Development will have extensive experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills. Essential Functions Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing. Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial); and in developing robust processes for pharmaceutical production. Directs projects and leads cross-functional teams with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget. Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs). Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors. Work cooperatively with, or lead, internal and external teams as required. Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators. Supports asset due diligence and new product introduction and integrations Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations. Assist other department team members in providing guidance / mentoring / reviewing documents / data in support of product development (e.g. clinical protocols, PK study results). Enhance and improve ways of working in Drug Product development, utilising knowledge of industry best practice Required Knowledge, Skills, and Abilities 10 – 15 years’ experience in drug product development in the pharmaceutical industry required. Direct experience with formulation development, process development, technical transfer and/or process validation. Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong track record in delivering achievements with meaningful impact in Pharmaceutical Development projects Demonstrated ability to lead cross-functional CMC Development teams Demonstrated troubleshooting and problem-solving skills including the use of designed experiments, statistical process control, Development/authorship of CMC regulatory filings for pharmaceutical products. Experience in defending processes, procedures and investigation during Regulatory Agency inspections desirable. Track record in generating intellectual property development. Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms. Excellent written and verbal communication skills, with demonstrated ability to communicate at executive leader level Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation. Proven project management skills for technical programs. Flexibility to travel on company business when required Required/Preferred Education and Licenses Master’s degree, PhD, or equivalent combination of education and work-related experience required. Description of Physical Demands Occasional mobility within office environment. Routinely sitting for extended periods of time. Constantly operating a computer, printer, telephone and other similar office machinery. 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: $(phone number removed) - $(phone number removed) 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

Senior Mechanical Building Services Manager (BSM) – Life Sciences Project Cambridge, UK Salary: Up to £90,000 + Package An exciting opportunity has arisen for an experienced Senior Mechanical Building Services Manager to join a major £18m MEP complex within a flagship life sciences park in Cambridge. This is a high-profile project delivering state-of-the-art facilities in one of the UK’s leading life sciences hubs. The Role You will take full responsibility for the mechanical package across a technically complex development, ensuring successful delivery from pre-construction through to commissioning and handover. This role is ideal for someone with strong commercial awareness and a proven track record in delivering high-value MEP projects. Key Responsibilities • Lead all mechanical building services activities on site, • Manage coordination of MEP design, installation, and commissioning, • Drive programme and ensure delivery to time, cost, and quality targets, • Oversee subcontractors, ensuring performance, safety, and compliance, • Liaise with consultants, clients, and project stakeholders, • Manage procurement, budgets, and value engineering opportunities, • Ensure adherence to UK building regulations and industry standards Requirements • Demonstrable experience as a Mechanical BSM or Senior Mechanical Manager, • Strong track record delivering complex MEP packages (£10m+ preferred), • Experience in life sciences, pharmaceutical, or similar environments advantageous, • Strong commercial and contractual awareness, • Excellent leadership, coordination, and communication skills, • Relevant engineering qualification (HNC/HND/Degree or equivalent) What’s on Offer • Salary up to £90,000 + competitive package, • Opportunity to work on a landmark Cambridge life sciences development, • Exposure to cutting-edge, technically challenging projects, • Clear career progression within a growing sector Apply Now If you’re looking to be part of a high-performing team delivering one of the UK’s most exciting life sciences projects, get in touch today

Our client has a permanent opportunity for a Scientific Product Specialist – Sales Support. They provide automation and fluid control solutions. As a key member of their talented and successful products team this is an interesting, varied, and challenging customer-facing role that is designed to support increase their market share. Working closely with the field sales team you will provide application, product knowledge and sale support during customer visits. The range of product focus include chillers, heat exchangers, sensors, media separated valves, clean wet pumps, and process gas controls. The key aspects we are looking for from applicants are: The person: • Strong relationship building skills, • Ability to provide value propositions, • An inquisitive nature Experience selling into: • Medical, • Life Science, • Hi-end processes manufacturing, • Pharmaceutical, • Semiconductors Product knowledge: • Thermo Controls, • 2 Port Valves, • Process Gasses To be considered you will need to demonstrate customer facing technical and sales experience. Key Responsibilities: Maintain accurate records of activities using our CRM system Grow sales of the product range through supporting the salesforce and their customers Understand and have the ability to use the value proposition of the product range responsible for and business value to grow sales. Identifying, researching, and gaining application knowledge for new opportunities for the product range. Promote the product range responsible for by creating marketing material, training material, and identifying trade shows where the range will achieve exposure. Develop strong working relationships with internal and external customers consulting with them to solve problems from a technical perspective. Meet and exceed targets. Skills and Experience: Desirable: A degree within a Science or Engineering discipline Required: HND or equivalent or relevant experience Proven track record of selling, specifying, or developing the product range of chillers, heat exchangers, sensors, media separated valves, clean wet pumps and process gas controls. Experience, skills and knowledge of the types of applications found in the non-invasive life science / medical / electronics industry, as these are the types of market areas, you will be working in. Demonstrate an ability to communicate and influence effectively at all levels of the business. Highly driven and passionate about making a difference within the industry. Proven track record of using value propositions to ensure customer satisfaction, increasing retention and customer loyalty to a brand. Full UK Driving Licence Current passport as European travel may be required. Due to the large number of responses we receive it is not always possible to respond to every application straight away. Should your skills and experience be a match for this role, or any other vacancy we may have, we will normally contact you within 72 hours of receiving your application. If you wish to apply for further roles please do so

Finance Systems & ERP Manager – Pharmaceutical / Medical industry. An international company in the medical industry is looking for a Business Systems Manager with good knowledge of the pharmaceutical / medical sector to join their team. The company is improving their Finance Systems and ERP soluti

Finance Systems & ERP Manager - Pharmaceutical / Medical industry. An international company in the medical industry is looking for a Business Systems Manager with good knowledge of the pharmaceutical / medical sector to join their team. The company is improving their Finance Systems and ERP solution

A great chance for an experienced Systems Accountant, ERP Manager or Financial Systems Manager with strong experience in the Pharmaceutical industry sector to take on the next challenge!. An international company in the medical industry is looking for a Systems Accountant or Financial Systems Manage