32 Svar Life Science jobs in Ireland

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

The Drug Products & Sciences R&D - Stability team supports R&D projects for new and existing products. We currently have an opening for a Research Associate II to represent Analytical Chemistry and Stability as a Stability Subject Matter Expert. The successful candidate would apply sound chemistry and stability planning knowledge to identify and evaluate stability indicating characteristics as part of product changes and new product development. The effective integration of chemistry and stability enables establishment of shelf life for new or existing products manufactured for rapidly growing markets and allows for the qualification of product changes on a global scale. The Stability Subject Matter Expert designs strategies and makes recommendations that may be non-routine to address technical, regulatory, and business requirements.

Essential Duties and Responsibilities:

• Represent R&D–Stability on project teams as a member of the project teams' goals and success.
• Support development and implementation of stability strategies for new product development and sustaining project activities.
• Support development of GMP stability studies used to establish expiration dating and support labeling for product development.
• Contribute to the development of technical justifications for expiration dating for new or modified products and the defense of expiration dating recommendation to key business partners.
• Provide valuable input to stability assessments and requirements for new products and/or current product changes.
• Ensure the right methods and specifications are available for stability, compatibility, and release testing. Ensure that the methods are appropriate for the product design over shelf life.
• Demonstrate the ability to identify risks, issues, and opportunities for improvement of existing methods, technologies, and approaches. Provide sound scientific rationale.
• Interact with manufacturing facilities to acquire information related to test methods and specifications.
• Author, review and verify technical data, protocols, and reports through use of Quality Documentation System.
• Act as study director for stability projects under guidance of senior Stability team members.
• Perform stability study administration activities on LIMS including study building and review, identification of product test data requiring modification, and data entry.
• Support development of new and/or optimization of existing processes and procedures to enhance stability related practices.
• Participate in investigations that correspond to atypical, out-of-specification, or out-of-trend test results. Review data and author technical evaluations that characterize the stability trending of suspect data under guidance of senior Stability team members.
• Leverage critical thinking to drive the investigation to conclusions based on sound scientific principles.
• Contribute to stability sections intended for submission to regulatory authorities under guidance of senior Stability team members. Use computerized systems to retrieve, evaluate, summarize data for reporting.

Qualifications required:

• Under guidance of senior Stability team member, able to organize complex information and demonstrate attention to detail.
• Logical and methodical when solving problems, developing solutions, and making sound recommendations with limited input from senior team members.
• Experience working with sophisticated databases.
• Possess relevant computer and technical skills including word processing, spreadsheets, table and graph generation, and use of databases and reporting tools.
• Good technical writing skills.
• Proficient in analytical chemistry including theoretical knowledge and practical experience.
• Willingness to contribute efforts beyond own scope of responsibilities to ensure project milestones are met.
• Basic functional understanding of FDA, ISO, and Quality systems.
• Works well in a team environment across multiple time zones and demonstrates an inclusive attitude.

Education:

• Bachelor's Degree with 2-4 years or Master's degree in a relevant scientific subject area.

What can Vantive offer to you:

• A stable and secure work environment
• A comprehensive benefits package, including private medical insurance, company pension scheme, and annual bonus scheme
• A collaborative and dynamic work environment
• Access to state-of-the-art equipment and technology
• Recognition and reward for outstanding performance

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

Recruitment Fraud Notice

Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

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Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

*POSITION SUMMARY: *
Assist in the clinical trial management to ensure timelines and metrics are met and maintained throughout the study. Provides support in the oversight and management of vendors. Conducts review of clinical data to ensure site adherence to applicable regulatory requirements, International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Good Clinical Practice (GCP) Guidelines, company standard operating procedures (SOPs), and study protocol.

*KEY RESPONSIBILITIES: *

• Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH GCP Guidelines, company SOPs, and study protocols. Ensure timelines and metrics are met and maintained throughout the study.
• Has a good knowledge of the therapeutic area and product.
• Obtains a complete understanding of all trial-related documents and operational procedures with moderate direct supervision

*Audits/Inspections/Quality Assurance (QA): *

• Supports with effective and timely audit/inspection responses.

*Clinical Trial Design/Performance: *

• Gains exposure/participates in case report form (CRF) development, interactive "X" recognition system (IXRS) set-up, central laboratory (lab) set-up, and other vendor selection processes and is capable of training others.
• Oversees completion of Pre-Study Visits (PSVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs), to determine protocol and regulatory compliance.
• Contributes to the resolution of escalated issues from study centers, regulatory authorities and institutional review board (IRBs)/independent ethics committees (IECs) with the support of the supervisor, if needed.
• Performs Sponsor Site Visits at selected sites to demonstrate oversight of the monitoring process and documenting the visits in the Sponsor Site Visit Report.
• Oversees study centers to ensure timely execution of the clinical studies, generating quality data ensuring the well-being of the study subjects and the trial integrity with moderate supervision.
• With the support from the supervisor, may support in the creation, review and tracking of study documents.
• May assist on the TMF reviews and resolution of findings, internally or interacting with the CRO with support if needed.

*Clinical Trial Materials (CTM): *

• Provides support on the regulatory document review and approval for investigational product (IP) release.
• Provides support in clinical product technical complaints and product recall as necessary.
• Provides support and information to the CTM staff regarding IP management, as needed.

*In-house Monitoring: *

• May assists with expedited identification, retrieval, and review of study documents particularly those required for site activation/study start-up.
• May facilitate investigator site payments, as applicable.

*Management/Training Team *
:

• Ability to facilitate meetings (e.g. Investigator Meetings, Kick-off meetings).
• May provide support for the monitor training and contribute to resolve the issues they identified.
• Collaborates in ensuring that appropriate training is conducted for CRO staff, vendors, investigators, and study site staff on study requirements and internal SOPs (if applicable).

*Monitoring: *

• Reviews and tracks comments of monitoring reports generated by the vendor (i.e. CRO) as part of Sponsor Oversight of Vendor Clinical Site Monitoring activities.
• With the support of the supervisor, if needed, verifies study documents (e.g., case report forms, source documents, adverse events) are tracked and reviewed for completeness and accuracy to ensure data integrity.
• Tracks study specific tasks and progress of the trial.
• Gets more insight, maintains and updates clinical trial management system (CTMS) information pertaining to the study.
• Is involved in the oversight of vendor clinical monitoring activities. Ensures that the clinical monitoring process is done in adherence to an international ethical and scientific quality standard to provide public assurance that the clinical data are credible.
• May collaborates with data management to resolve queries.

*Vendor Management: *

• Assists in the management of vendor performance during conduct of the study with moderate direct supervision.
• Assists in evaluation of vendor performance during conduct of the study.
• Reviews/creates/tracks trial newsletters, memos, mass correspondence, or other appropriate trial-related documentation, with moderate supervision.
• Facilitates the scheduling of internal team meetings, cooperating with defining the agenda and creating the meeting minutes, if needed.

*In-house Monitoring: *
Additional On-site Monitoring Responsibilities:

• Performs monitoring/co-monitoring activities for site initiation visits, interim site monitoring, and closeout visits, in conformance to all relevant laws, regulations, guidelines and internal SOPs/policies.
• Identifies/screens/qualifies investigators through feasibility questionnaires and pre-study visits.
• Reconciles clinical supplies and drug accountability records at study sites.
• Verifies study documents (e.g., case report forms, source documents, adverse events) are tracked and reviewed for completeness and accuracy to ensure data integrity.
• Identifies and effectively documents site findings with an equal ability to re-train, place corrective action in place with the site, and follow-up as required.
• Reviews, clarifies, and obtains, data changes via query resolutions with site personnel.
• Conducts completion of PSVs, SIVs, IMVs, and COVs, to determine protocol and regulatory compliance.
• Prepares telephone contact reports, confirmation letters, site visit reports (PSV, SIV, IMV, and COV), and follow-up letters to accurately and completely document site status and activities in agreement with the Clinical Monitoring Plan for the study.

*Monitoring: *

• Assists with expedited identification, retrieval, and review of study documents particularly those required for site activation/study start-up.

Safety:

• Understands and supports implements processes for distribution and tracking of SAE's, safety documentation, and pregnancies. Monitors compliance of these processes.

PERSON SPECIFICATION

• Typically requires 2 years of experience in clinical research, including a minimum of 1-year field monitoring experience (e.g., independent monitoring, co-monitoring, accompanied site visits).
• Associate's degree in a life science field required.
• Relevant experience in clinical research and field monitoring experience preferred (e.g. independent field monitoring and co-monitoring).
• 4 years clinical research experience with 2 years experience as a CRA
• Bachelor's degree or higher degree in a life science field preferred.

*Our Benefits Include: *

• Highly competitive salary
• Group pension scheme - Contribution rates are (1.5% / 3%/ 5%/ 7%) and company will match
• Private Medical Insurance for the employee (Irish Life)
• Ongoing opportunities for career development in a rapidly expanding work environment
• Succession planning and internal promotions
• Education allowance
• Wellness activities - Social activities eg. Padel, Summer Events

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

Location: EMEA : Ireland : Dublin | EMEA : Ireland : Home Office:Grange Castle (Dublin)
Learn more about Grifols

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

The Drug Products and Sciences R&D Stability team supports research and development projects for new and existing products. The
Research Associate III, Stability Subject Matter Expert
, applies sound chemistry and stability planning expertise to identify and resolve stability indicating characteristics. The effective integration of chemistry and stability enables establishment of shelf life for new or existing products manufactured for rapidly growing markets and allows for the qualification of product changes on a global scale. The Stability Subject Matter Expert develops and designs strategies and makes recommendations that are non-routine to address technical, regulatory, and business requirements.

Essential Duties And Responsibilities

• Represent R&D–Stability on project teams as a key member of the project teams' goals and success.
• Craft and implement stability strategy plans for new product development and sustaining projects.
• Design GMP stability studies used to establish expiration dating for product development.
• Contribute to the development of technical justifications for expiration dating for new or modified products and the defense of expiration dating recommendation to key business partners.
• Provide valuable input to stability assessments and requirements for new products and/or current product changes.
• Ensure the right methods and specifications are available for stability, compatibility, and release testing. Ensure that the methods are appropriate for the product design over shelf life.
• Demonstrate the ability to identify risks, issues, and opportunities for improvement of existing methods, technologies, and approaches. Provide sound scientific rationale.
• Interact with manufacturing facilities to acquire information related to test methods and specifications.
• Author, review and verify technical data, protocols, and reports.
• Act as study director for stability projects under guidance of senior Stability team members.
• Perform stability study administration activities on LIMS including study building and review, identification of product test data requiring modification, and data entry.
• Develop new and/or optimize existing processes and procedures to enhance stability related practices.
• Participate in investigations that correspond to atypical or out-of-specification/out-of-trend test results. Review data and author technical evaluations that characterize the stability trending of suspect data.
• Leverage critical thinking to drive the investigation to conclusions based on sound scientific principles.
• Optimally plan, coordinate, and oversee the progress of multiple Stability related projects, budgets, and activities working with global teams and CROs as applicable.
• Contribute to and/or take lead author role for stability sections intended for submission to regulatory authorities. Use computerized systems to retrieve, evaluate, summarize data for reporting.

Education And Experience

• Bachelor's Degree with 5-7 years, Master's with 3-5 years, or PhD with 0-3 years' experience in a relevant scientific subject area.
• Ability to organize complex information and demonstrated attention to detail.
• Apply a logical, methodical approach in independently solving problems, developing solutions, and making sound recommendations.
• Experience working with sophisticated databases.
• Possess relevant computer and technical skills including word processing, spreadsheets, table and graph generation, and use of databases and reporting tools.
• Good technical writing skills.
• Possess proficiency in analytical chemistry including theoretical knowledge and practical experience.
• Contribute to efforts beyond own scope of responsibilities to ensure project milestones are met.
• Functional understanding of FDA, ISO, and Quality systems.
• Willingness to work in a team environment across multiple time zones and demonstrates an inclusive attitude.

What Can Vantive Offer To You

• A stable and secure work environment
• A comprehensive benefits package, including private medical insurance, company pension scheme, and annual bonus scheme
• A collaborative and dynamic work environment
• Access to state-of-the-art equipment and technology
• Recognition and reward for outstanding performance

Reasonable Accommodation
Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

Recruitment Fraud Notice
Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

About TriviumVet - A PBI Gordon Company

TriviumVet is an innovative veterinary pharmaceutical research and development company based in Waterford city, in Ireland's sunny southeast. We're a small, dynamic team with deep expertise across veterinary science, regulatory affairs, quality, analytical development, and pharmaceutical formulation. Our mission is simple: improve the lives of pets by addressing unmet needs in companion animal medicine.

We develop therapeutics and diagnostics for diseases where treatment options are limited, and our products aim to make a meaningful difference to animals, veterinarians, and pet owners alike. Our lead product, FELYCIN-CA1, was recently conditionally approved by the FDA for use in cats with subclinical hypertrophic cardiomyopathy, providing the first treatment option for the millions of cats with this disease in the United States.

Who You Are

• A qualified veterinary surgeon (MVB, MRCVS, or equivalent).
• Ideally with 2–5 years of experience in companion animal clinical practice.
• Interested in science, research, and making a broader impact on animal health.
• Eager to learn and contribute to a close-knit, interdisciplinary team.
• Skilled in communication, organization, and scientific reasoning.
• Proficient in Microsoft Office (especially Excel); familiarity with biostatistics is a plus.
• Comfortable managing multiple responsibilities in a fast-paced environment.

Key Responsibilities

• Assist in the design, conduct, and monitoring of field and laboratory clinical studies.
• Write, review, and manage clinical documentation (e.g., study protocols, SOPs, data

forms, reports).

• Monitor study sites and assist in ensuring high-quality data collection and regulatory compliance.
• Support interpretation and analysis of clinical data and communicate findings to internal teams and stakeholders.
• Conduct literature reviews and contribute to study design and regulatory strategy.
• Liaise with veterinary investigators, Contract Research Organisations, and other study partners.
• Help prepare regulatory submissions for global authorities (CVM – The Center for Veterinary Medicine at the FDA, CVMP - Committee for Veterinary Medicinal Products at the European Medicines Agency (EMA)).
• Ensure studies adhere to Good Clinical Practice (GCP) and Good Laboratory Practice (GLP).
• Track project progress against timelines and budgets.
• Participate in cross-functional project planning and problem-solving.

Why Join TriviumVet

• Impactful Work: Contribute to the development of new therapies that are groundbreaking first-to-market treatments which enhance the lives of pets and their owners.
• Veterinary Career Development: Gain in-depth experience in clinical research and regulatory affairs with support from senior team members.
• Broad Exposure: Learn about pharmaceutical R&D, manufacturing, and regulatory strategy from a cross-functional perspective.
• Flexible Working: Blend of remote and on-site work in a friendly, collaborative environment.
• Great Location: Enjoy life in Waterford — Ireland's sunny southeast — with easy access to nature, culture, and coastal living.
• Competitive Salary: Reflective of experience, with opportunities for progression. Bonus and long term incentive opportunities available once probationary period complete.

To Apply

If you're a veterinary surgeon ready to step beyond clinical practice and contribute to veterinary innovation, we'd love to hear from you.

We're not looking for a perfect CV — we're looking for curiosity, capability, and a commitment to improving animal health thorugh science.

Send your CV and cover letter to

Reporting directly to the Technical Manager in their area, the
Laboratory Scientist
– Inorganic Chemistry
is responsible for assisting with delivering a quality service to Uisce Éireann and its customers, complying with the requirements of the Quality management system and ISO17025 standard. This will be achieved by contributing to team performance and the efficient and effective use of resources. They will participate in the day-to-day operation of the laboratory, carrying out sample preparation, analysis and reporting duties for Water Samples for Uisce Éireann (UÉ) as required.

Purpose of the Role:
The purpose of this post is to assist in the delivery of NPT services in CHI Temple St., CHI Crumlin (including support to CHI UCC at Connolly and Tallaght) with the ultimate aim of achieving compliance with ISO 22870 Near Patient Testing Requirements for Quality and Competence, and ISO 15189:2012 Medical Laboratories - Particular Requirements For Quality And Competence standards.

Essential Criteria:
Candidates must, on the latest date for receiving completed application forms for the post, possess:

• Bachelor in Science (Applied Science) Honours degree (Biomedical option) from the Technological University Dublin, or previously DIT Kevin Street

or

• Bachelor in Science Honours degree in Biomedical Science from University College Cork – Cork Institute of Technology course

or

• Diploma in Medical Laboratory Sciences of the Dublin Institute of Technology, Kevin Street of the Cork Institute of Technology awarded prior to 1994

or

• Possess Certificate in Medical Laboratory Sciences of the Dublin Institute of Technology. Kevin Street or Cork Institute of Technology or the Galway/ Mayo Institute of Technology (awarded prior to 1997)

or

• A recognised qualification at least equivalent to the above

and

• Be a member, or be eligible for membership, of the Academy of Clinical Science and Laboratory Medicine (ACSLM)

And

• Be CORU Registered

How to Apply and Informal Enquiries:
Applications for this post must be accompanied by a cover letter, setting out relevant experience that illustrates how the essential criteria listed above is met.

The criterion for short listing is based on the requirements of the post, as outlined in the eligibility criteria.

• Please note that you must submit a cover letter with your CV, this forms part of your application and CV's will not be accepted without a detailed cover letter.

The closing date for submissions of CV's and cover letter is
Thursday 6thNovember 2025 at 11.45pm.
Applications must be completed through the advertised post on

by clicking
'Apply for Job'.
Applications will not be accepted through direct email or any other method.
For informal enquiries for this specialty/department, please contact Martina Ring at

For other queries relating to this recruitment process, please contact Talent Acquisition

PLEASE NOTE:
CHI has transitioned to a process of a one commencement day per month for all new employees, CHI internal transfers and Secondments. This update to our Onboarding process is aligned to changes in our monthly/fortnightly payroll and with the launch of our new corporate induction program. This process enhancement ensures that we can thoroughly prepare for your arrival and facilitate a smooth transition in your onboarding journey.

It is important for you to note that if you do not have your pre-employments and mandatory training completed in time, your commencement date will be deferred to the next available date.
Below, you'll find the list of commencement dates for 2025.

• December 15th 2025
• January 7th 2026
• January 12th NCHD rotation only)
• February 9th 2026
• March 9th 2026

Role:
Medical Scientist (Haemotology/Bloodtransfusion)

Location
: North Dublin

Contract:
3 year specified purpose contract

Hours:
Full-time, 35 hours per week, over five days per week, plus on call obligation (pro rata)

Salary:
HSE salary scale, aligned with experience

Join a hospital that truly values its people where support, professional development, and staff wellbeing come first. With a reputation for exceptional staff retention, long service, and a genuine commitment to workplace wellness, this is your opportunity to thrive in a positive, collaborative, and forward-thinking laboratory environment.

Excel Recruitment are seeking a dedicated and experienced
Staff Grade Medical Scientist on behalf of a dynamic Haematology/Blood Transfusion
department within a highly regarded hospital in north Dublin.

This role offers you the opportunity to work under the leadership of a highly supportive Chief Medical Scientist and laboratory manager, who fosters a collaborative and empowering work environment.

The successful candidate
will be responsible for delivering high-quality diagnostic services, ensuring the accuracy and efficiency of laboratory results, and contributing to the overall patient care pathway. You will play a crucial role in the ongoing success of the growth and expansion of the laboratory.

On Call Rota:
Candidates will be placed on the multi-disciplinary (Biochemistry/Haematology/Blood Transfusion) on-call Rota contingent upon the Hospital being satisfied that they have the required competency and experience to work on call.

Key Responsibilities:

• Perform routine laboratory scientific work to the highest standard in accordance with the Department's policies, procedures, and guidelines.
• Receive training and maintain competence in all relevant areas of the laboratory services.
• Support colleagues and work collaboratively with all team members.
• Participate in service development and improvement.
• Participate in evaluating equipment, reagents, and consumables.
• Assist in ensuring compliance with international and national guidelines and standards for the provision of service and actively participate in internal quality control and external quality assessment.
• Participate in performance review and development and in continuous professional development.
• Adhere to all laboratory's standard operating procedures, policies, and guidelines.
• Participate in facilitating arrangements for educating and training staff.

Qualifications:

• BSc in Medical Science or equivalent
• Current registration with CORU or eligibility for registration is required.
• Knowledge and experience of working in an ISO15189 accredited Medical Laboratory.
• Experience using a Laboratory Information Management System
• Excellent communication skills, both written and verbal, with the ability to explain complex information to non-specialists.
• Ability to work on own initiative
• Team Player
• Good Communication Skills

Your rewards:

• Competitive salary, comprehensive benefits package and competitive annual leave 27 days.
• Paid sick leave
• Free Parking
• Flexible work patterns
• You will be eligible to join an excellent defined contribution (DC) Pension scheme.
• Full paid maternity leave
• Subsidised hospital restaurant
• A positive and collaborative work environment
• A strong commitment to continuous professional development for employees, providing numerous opportunities for growth and career advancement.
• Commitment to work-life balance and employee wellness.
• You will become part of an outstanding team, where you will have access to cutting edge technology and resources.
• Many of the top Irish medical consultants practice in this hospital
• You will be employed in a cohesive and expanding environment with a history of rewarding excellence, supporting your career growth through continuous learning and development.
• Supportive leadership that values innovation and excellence.

How to Apply:

Whether you're an experienced Medical Scientist ready to take the next step, or a recent graduate eager to begin your career, we'd love to hear from you. Please contact Charlene Cooke

by email or by telephone