Be part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.
What you’ll do:
Maintaining and Fixing equipment at a leading Bio pharm ManufacturerElectrical Competency is a primary requirement and Mechanical are also desired to some degreeHelp with Continuous Improvement and highlight opportunities for positive changeWho you are:
Minimum of a recognized national apprenticeship in a practical engineering discipline, desired HNC or HND in an engineering disciplineGood Industrial safety knowledge and understanding of roles and responsibilities in legislationIt would be a plus if you also possess previous experience in:
Manufacturing environmentWorking within ISO Class cleanroomsExperience with plant and equipment installationJoin our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessWorking at Cytiva means being at the forefront of providing new solutions to transform human health.
As Manufacturing Engineer/Technician it will be your responsibility to provide support to the manufacturing operations team to help improve productivity, reduce costs and deliver quality products. You will be based on-site at our Cytiva Ilfracombe plant in North Devon.
What you will do:
• Support operations in the day to day running of the production machinery and processes.
• Work within a multifunction environment to solve complex and/or urgent issues.
• Respond to key performance indicators, i.e. delivery, productivity.
• Define and implement cost savings and/or improvement ideas
• Deliver, chair or attend meetings when required to do so.
Who you are:
• Possess good analytical skills to help drive and measure improvements.
• Able to demonstrate a broad experience of manufacturing processes and equipment
• Proven ability to manage multiple projects successfully.
• Excellent problem-solving skills and able to drive through improvements.
• Excellent oral and written communication skills with ability to present information concisely and effectively.
Travel, Motor Vehicle Record & Physical/Environment Requirements:
• Must be willing and able to travel, both inside and outside the UK, for approx. 10% of your time.
• Must have a valid driver’s license with an acceptable driving record
• Ability to lift, move or carry equipment
It would be a plus if you also possess previous experience in:
• Able to create FMEA’s and Risk assessments to form part of the change control process
• Working knowledge of AutoCAD Inventor Drawing Package and VAULT.
• Had previous experience in managing others
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessBe part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.
We have an exciting opportunity for a Senior Product Engineer!
What you’ll do:
Lead and support local and/or global projects by effective use of Visual Project and Daily Management tools to ensure on-time and on-cost project delivery.Instigate and lead direct communications cross-functionally within Cytiva and with our suppliers and customers.Generate ideas for Global Kaizen Funnel and utilise problem solving tools to resolve technically challenging complex problems through innovative solutions.Lead / facilitate Kaizen events.May include New Product Introduction creating and challenging project requirements for new product designs whilst fostering innovation and sustainability.Product, Process and Equipment Validation involving validating testing plans and data review, test regimes based upon knowledge and experience.Work using own initiative, prioritizing work as appropriate whilst maintaining a cross-functional team approach.May have leadership responsibilities for a small team.Mentor team members within local Product Engineering team.Who you are:
You are action oriented, have an analytical mindset and are always looking to optimize work processes.Lead and collaborate across teams within Cytiva, Pall or external entities creating trusted relationships.Build and maintain effective and constructive working relationships, partnerships or networks with people who are instrumental in achieving work-related goals.You understand product performance, developing robust and repeatable processes in-line with these requirements.Appropriately incorporate multiple inputs to establish shared ownership and effective action.An overall achievement mindset, a bias for action and eagerness to take the initiative.Ability to travel globally where and when required.It would be a plus if you also possess previous experience in:
A recognized Engineering Certificate/Degree or equivalent and subsequent experience in product development or manufacturing.Demonstrable knowledge of chemistry / polymer science.Familiar with multiple software platforms, procedures, and techniques relevant for this function.Demonstrable knowledge of process validation procedures and techniques (IQ, OQ and PQ) documents for new products, processes, and equipment.Conversant with English language.Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessBe part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Regulatory Affairs Specialist for Cytiva is responsible for supporting regulatory compliance of Medical Devices placed on the market in EMEA.
This position is part of Medical Regulatory Affairs located in Portsmouth, UK and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Compile all aspects of Technical Documentation for product certification under Regulation (EU) 2017/745 for Medical Devices.Submit Technical Documentation to Notified Bodies for review and approval.Support RA related QMS documentation, Complaints Assessment, Vigilance Reports and Change Controls.Support medical device Regulatory Intelligence process and customer requests.Provide support as required for UK Responsible Person with regard to the requirements set out in the UK MDR 2002 relating to medical devices.Participate in and support activities associated with the Medical Regulatory Affairs team objectives, as directed by line manager.Who you are:
You have a Life Sciences degree or equivalent.You have at least 2-3 years experience in a healthcare / life sciences industry in a regulatory or technical field.Working knowledge of Medical Device regulations (EU MDR, MDCG guidelines, other EMEA), ISO 13485 and ISO 14971.Experience with Quality Management System documentation.Ability to communicate effectively across all departments and functionsGood attention to detail.Have excellent English oral and written communication.The ability to present technical, product and regulatory information clearly and concisely.Travel, Motor Vehicle Record & Physical/Environment Requirements:
Ability to travel required at 10% or less within the EMEA region.Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessBe part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Regulatory Affairs Specialist for Cytiva is responsible for supporting regulatory compliance of Medical Devices placed on the market in EMEA.
This position is part of Medical Regulatory Affairs located in Portsmouth, UK and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Compile all aspects of Technical Documentation for product certification under Regulation (EU) 2017/745 for Medical Devices.Submit Technical Documentation to Notified Bodies for review and approval.Support RA related QMS documentation, Complaints Assessment, Vigilance Reports and Change Controls.Support medical device Regulatory Intelligence process and customer requests.Provide support as required for UK Responsible Person with regard to the requirements set out in the UK MDR 2002 relating to medical devices.Participate in and support activities associated with the Medical Regulatory Affairs team objectives, as directed by line manager.Who you are:
You have a Life Sciences degree or equivalent.You have at least 2-3 years experience in a healthcare / life sciences industry in a regulatory or technical field.Working knowledge of Medical Device regulations (EU MDR, MDCG guidelines, other EMEA), ISO 13485 and ISO 14971.Experience with Quality Management System documentation.Ability to communicate effectively across all departments and functionsGood attention to detail.Have excellent English oral and written communication.The ability to present technical, product and regulatory information clearly and concisely.Travel, Motor Vehicle Record & Physical/Environment Requirements:
Ability to travel required at 10% or less within the EMEA region.Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessBring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Product Engineering Support Technician is responsible for supporting the Product Engineering team based In Ilfracombe in a range of product life cycle activities (NPI, Mould tool changes, Material changes and Sustainment, internal NCR reduction and external POR reduction) for Cytiva.
This position reports to the Product Engineering Team Lead and is part of the Product Engineering team located in the clean room in Ilfracombe, UK and will be an on-site role.
What you will do:
Support the Product Engineering team to carry out experiments, trials, DOE and validation activity for both product and equipment improvements.To provide written and verbal summaries of engineering studies carried out.Set up and optimize manufacturing equipment to support the development of new products and machinery.Who you are:
Competent in I.T. practices and experience of common Microsoft applicationsMinimum 1 years relevant experienceA recognised engineering qualification and/or relevant experience demonstrating a practical hands-on approach.Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
Ability to travel – occasional not mandatoryDesirable to have a valid driver’s license with an acceptable driving recordIt would be a plus if you also possess previous experience in:
Local manufacturing knowledge covering multiple manufacturing process stepsAbility to work as part of a team towards completion of product improvement projects.Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessBring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Manufacturing Engineer is responsible for supporting day-to-day operations including production associates, equipment, and processes to ensure we provide the highest quality products to our customers. The Manufacturing Engineer also provides technical and project leadership to develop and deploy equipment and process upgrades for new product development, cost reduction and quality improvement.
This position reports to the Tech Transfer Team Leader and is part of the Operations & Supply Chain team located in Stevenage and will be an on-site role.
What you will do:
Identify, participate in and lead projects that deliver improvements in safety, quality, delivery and costProblem solve process issues and/or product non-conformances using empirical evidence and quantitative analysisParticipate in New Product Development projects and support the transfer of new products from development into productionCreate process and validation documentation to ensure manufacturing is performed safely and meets the documented quality specificationsMaintain full regulatory compliance with EHS, quality and legal requirementsWho you are:
Bachelor’s degree in Mechanical, Manufacturing or Process Engineering (or a related field) with more than 5 years of relevant experienceExperience of applying lean manufacturing tools including Daily Management, Standard Work and Lean ConversionEquipment and process design and improvement in a regulated industryExcellent communicator (written & verbal), comfortable interacting at all levels of the organisationAble to work independently and collaborate well across diverse functions in a matrix organisationTravel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
Able to travel within UK/Europe in support of the role objectives (estimated at 10%)Must have a valid driver’s license with an acceptable driving recordIt would be a plus if you also possess previous experience in:
Clean room environments in the Pharmaceutical or Medical Device industryFormal training, qualification and proven experience in Six Sigma techniquesCytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessWorking at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
Cytiva’s Membrane Chromatography R&D team, is looking for a leader for its Chemistry department, based at their new state of the art R&D facility in Sycamore House, Stevenage. The successful candidate will be responsible for leading a team of chemists and technicians, focused on developing Cytiva’s next generation membrane chromatography products. The Chemistry team’s core remit involves developing the synthetic pathways and chemistry processes used to modify and functionalise our proprietary membranes, enabling them to be used in the production of biotherapeutics such as monoclonal antibodies and genomic medicines . The team therefore plays a key role in developing and optimizing the performance of Cytiva’s new and evolving range of Fibro chromatography products.
What you’ll do
As the Manager of the Chemistry team, you will provide direction by translating high level strategies into tangible group objectives and deliverables. You will lead a multidisciplinary team of chemists and scientists, providing mentorship, performance management, career development and technical guidance.
You will act as a subject matter expert (SME) in the field of synthetic organic chemistry, with a deep expertise in surface chemistry and bioconjugation, which you’ll leverage to provide technical input to project teams focused on developing the next generation of membrane chromatography bioprocessing solutions. You will also be expected to represent the Chemistry team in cross organizational forums, strategic planning sessions and customer engagements.
As a member of the R&D Leadership team, you will partner with material science, engineering, applications and analytical team leaders in order to align strategic and tactical Chemistry objectives with other R&D functions. As well as the local team of scientists in Stevenage, you’ll also have the opportunity to work with Chemistry and R&D teams from across Cytiva’s global network.
Key Responsibilities include
· Oversee the development of surface chemistry and bioconjugation approaches for modifying and functionalizing Cytiva’s chromatography membranes.
· Leading and providing direction to the R&D Chemistry team at Cytiva Stevenage by setting clear objectives, conducting regular performance reviews and supporting career development for all team members
· Define and drive the chemistry roadmap for Cytiva’s membrane chromatography products in alignment with company innovation and commercial objectives.
· Work across functional boundaries by coordinating Chemistry development activities with other Cytiva R&D teams
· Supporting progression of R&D projects, directed towards New Product Introductions (NPIs), and the improvement of existing Cytiva products
· Managing projects and stakeholder expectations to ensure alignment of defined project deliverables and realised project outcomes.
· Authoring and overseeing the detailing of documentation, including technical reports and patent filings and ensuring that all technical documents written by the chemistry team maintains a consistent high standard and that documentation meets all requirements of the Cytiva QMS
· Leveraging Cytiva’s robust QMS systems and tools to facilitate and manage design transfer from R&D to Cytiva’s manufacturing and supply chain teams, and with relevant Contract Manufacturing Organisations
· Responsible for health and safety of the chemistry team, working closely with the EHS lead to ensure that risk assessments are in place for all processes and providing guidance around chemical safety
· Contributing towards the short, medium and long term chemistry development strategy for Cytiva’s range of membrane chromatography products
· Drive the use of Danaher Business System (DBS) tools, including but not limited to daily management, Kaizen and Problem Solving Process (PSP)
Job Requirements
· PhD or equivalent higher-level qualification in Organic Chemistry or related discipline with 8+ years’ of relevant industrial experience, including 3+ years in a leadership role
· Demonstrated expertise in synthetic organic chemistry, with a particularly specialisation in surface modification and bioconjugation
· Hands-on experience with analytical chemistry techniques (e.g HPLC, LC-MS, FT-IR, Raman and UV/Vis) and surface characterisation methods (e.g. SEM)
· Experience of working on multidisciplinary projects and working at the interface between chemistry and biology
· Strong leadership and communication skills, with experience managing technical teams and cross-functional projects
· Track record of demonstrating strong problem-solving skills and ability to work independently in a fast-paced multidisciplinary environment
Preferred Knowledge & Experience
· Knowledge in the field of material sciences is desirable
· Experience with membrane or polymer surface funtionalisation is desirable
· Experience in chromatography, membrane filtration or bioprocessing is desirable
· Experience in reactor design/ process engineering is desirable
· Familiarity with GMP/ GLP environments and documentation practices is desirable
When you join us, you’ll also be joining Danaher’s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read LessBe part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.
Summary of purpose of role.
Responsible for developing, implementing, and optimizing production processes to ensure efficient, safe, and cost-effective operations. Minimize equipment downtime and enhance productivity by leading continuous improvement initiatives driven by performance data and root cause analysis.
Work with maintenance and production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment, and product design.Use root cause analysis to solve complex manufacturing and quality issuesDevelop manufacturing and/or testing processes with focus on safety, quality, and repeatability for New Product Introduction/Sustainment projects.Follow best practices around Process Development (PD), Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) with a goal to develop Safe and Quality ProcessesCreate standard operating procedures (SOP) or work instructions and provide training and guidance to othersMonitor and analyse equipment performance, driving continuous improvement projects.Position Competencies:
Hold formal qualifications (Bachelors Degree) in an Engineering discipline or time served in a Process/Manufacturing role.Strong Process Engineering background and a detailed understanding of process validation requirements in a manufacturing environment.Works well under time-bound pressure as part of a team, and independently.Strong documentation skills (work instructions, manufacturing plans etc) with a keen eye for detailSelf-motivated and committed to upholding high standards of Safety, Quality and Delivery.Ability to communicate effectively across all departments and functions.Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Read Less