3 Research Lab jobs in Ireland
Assoc Research Scientist (Technical Lead) - Biopharma - Athlone, Ireland
Athlone, Leinster
ThermoFisher Scientific
Posted 27 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Assoc Research Scientist - Biopharma**
At PPD, part of Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We have a great opportunity for an Associate Research Scientist to join our growing Biopharmaceutical team. This role is a Technical Lead position based at our Analytical GMP facility in Athlone, Ireland.
**Location/Division Specific Information**
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
**Discover Impactful Work:**
The role of Associate Research Scientist is responsible for the regulatory and scientific conduct of development and stability projects in the Biopharmaceutical Laboratory. Performs troubleshooting across multiple assay formats, clients and cell lines. Calculates and interprets data and records data in adherence with PPD SOPs and any additional requirements specific to the lab and/or client.
**A day in the life:**
+ Independently performs analytical testing, method optimization/validation, and/or other speciality technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods, and protocols applicable to assigned tasks. Designs and completes experiments independently.
+ Reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.
+ Prepares and reviews study protocols, project status reports, final study reports and other project-related technical documents.
+ Communicates data and technical issues to clients on a weekly basis (or as needed).
+ Provides technical mentorship and training to staff.
+ Leads analytical (procedural and instrumental) troubleshooting sessions.
+ Assists in preparation and implementation of SOPs and quality systems.
+ Reviews, interprets, and analyses data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
**Education and Experience**
+ Degree or equivalent in Chemistry or Biochemistry
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
**Knowledge, Skills, Abilities**
+ Knowledge of general chemistry, biochemistry techniques (Western Blot, total protein by BCA or micro BCA assay, ELISA, HPLC/UPLC)
+ Proven experience of method development of identity and purity assays by Western Blot.
+ Ideally experience in leading CMC studies for biopharmaceutical products including method validation
+ Proficiency on technical operating systems (including Image Lab software)
+ Proven problem solving and troubleshooting abilities
+ Ability to independently perform root cause analysis for method investigations
+ Proven ability in technical writing skills
+ Time management and project management skills
+ Good written and oral communication skills
+ Ability to work in a collaborative work environment with a team
+ Ability to train junior staff
**Work Environment**
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
+ Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
+ Able to work upright and stationary and/or standing for typical working hours.
+ Able to lift and move objects up to 25 pounds.
+ Able to work in non-traditional work environments.
+ Able to use and learn standard office equipment and technology with proficiency.
+ May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
+ Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today!** ** Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
**Accessibility/Disability Access**
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1- *. Please include your contact information and specific details about your required accommodation to support you during the job application process.
+ This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
**_We welcome and encourage applicants from outside of Ireland. We can provide support with immigration and visa needs for successful applicants and dependents, tax consultations and other basic destination services. All other relocation costs are at the expense of the applicant._**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Assoc Research Scientist - Biopharma**
At PPD, part of Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We have a great opportunity for an Associate Research Scientist to join our growing Biopharmaceutical team. This role is a Technical Lead position based at our Analytical GMP facility in Athlone, Ireland.
**Location/Division Specific Information**
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
**Discover Impactful Work:**
The role of Associate Research Scientist is responsible for the regulatory and scientific conduct of development and stability projects in the Biopharmaceutical Laboratory. Performs troubleshooting across multiple assay formats, clients and cell lines. Calculates and interprets data and records data in adherence with PPD SOPs and any additional requirements specific to the lab and/or client.
**A day in the life:**
+ Independently performs analytical testing, method optimization/validation, and/or other speciality technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods, and protocols applicable to assigned tasks. Designs and completes experiments independently.
+ Reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.
+ Prepares and reviews study protocols, project status reports, final study reports and other project-related technical documents.
+ Communicates data and technical issues to clients on a weekly basis (or as needed).
+ Provides technical mentorship and training to staff.
+ Leads analytical (procedural and instrumental) troubleshooting sessions.
+ Assists in preparation and implementation of SOPs and quality systems.
+ Reviews, interprets, and analyses data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
**Education and Experience**
+ Degree or equivalent in Chemistry or Biochemistry
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
**Knowledge, Skills, Abilities**
+ Knowledge of general chemistry, biochemistry techniques (Western Blot, total protein by BCA or micro BCA assay, ELISA, HPLC/UPLC)
+ Proven experience of method development of identity and purity assays by Western Blot.
+ Ideally experience in leading CMC studies for biopharmaceutical products including method validation
+ Proficiency on technical operating systems (including Image Lab software)
+ Proven problem solving and troubleshooting abilities
+ Ability to independently perform root cause analysis for method investigations
+ Proven ability in technical writing skills
+ Time management and project management skills
+ Good written and oral communication skills
+ Ability to work in a collaborative work environment with a team
+ Ability to train junior staff
**Work Environment**
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
+ Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
+ Able to work upright and stationary and/or standing for typical working hours.
+ Able to lift and move objects up to 25 pounds.
+ Able to work in non-traditional work environments.
+ Able to use and learn standard office equipment and technology with proficiency.
+ May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
+ Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today!** ** Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
**Accessibility/Disability Access**
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1- *. Please include your contact information and specific details about your required accommodation to support you during the job application process.
+ This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
**_We welcome and encourage applicants from outside of Ireland. We can provide support with immigration and visa needs for successful applicants and dependents, tax consultations and other basic destination services. All other relocation costs are at the expense of the applicant._**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
0
Dosimetry Lab Technician
Kilkenny, Leinster
Abbott
Posted 27 days ago
Job Viewed
Job Description
**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
**Abbott Diabetes Care Kilkenny**
Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems.
**Main Purpose of the Role**
Responsible for maintaining the effectiveness of the dosimetry lab and dosimetric product release in accordance with GLP, GMP and regulatory requirements. Ensure compliance to site and divisional policies and procedures. Support continuous improvement activities. Adhere to Health and Safety within the working environment, highlight opportunities for improvement to EHS performance.
**Main Responsibilities**
+ Perform a variety of sampling activities to support product manufacture in a cGMP regulatory environment.
+ Perform dosimetric analysis, dose map execution and equipment maintenance, accordance with GLP, GMP and ISO 11137.
+ Ensure that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs).
+ Assist in the design and set-up of the site dosimetry lab program.
+ Create and update documentation as needed.
+ Support the set up and maintenance of laboratory equipment and consumables.
+ Ensuring the laboratory is adequately stocked and resourced, with everything accurately labelled.
+ Participate in validation activities as needed for dosimetry lab and equipment qualification program.
+ Review and approval of laboratory test results.
+ Complete records on time and review data for accuracy and completeness.
+ Assist in the identification of root cause analysis and provide technical advice as needed.
+ Support unplanned events and raise out of specification results in a timely manner and inform the Supervisor immediately of any such events.
+ Initiate and complete CAPAs and change controls in accordance with site procedures.
+ Trend data for environmental and product monitoring. This also involves the generation and presentation of quarterly and annual reports
+ Maintain a "right first time" approach to quality records by ensuring accountability for functional responsibilities.
**Qualifications & Experience**
+ Third level Science / Manufacturing or equivalent qualification.
+ Preferred two years' work experience in a Manufacturing / Science / Quality or equivalent environment.
+ Electron beam or other sterilisation technologies experience desirable.
+ Knowledge in ISO 11137 desirable.
+ Chemistry/Microbiology/Dosimetry Lab experience desirable.
**What we Offer:**
Attractive compensation package that includes competitive pay, as well as benefits such as
+ Family health insurance
+ Excellent pension scheme
+ Life assurance
+ Career Development
+ Fantastic new facility
+ Growing business plus access to many more benefits.
Connect with us at and on LinkedIn , Facebook , Instagram , X and YouTube .
Abbott is an equal opportunities employer.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
**Abbott Diabetes Care Kilkenny**
Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems.
**Main Purpose of the Role**
Responsible for maintaining the effectiveness of the dosimetry lab and dosimetric product release in accordance with GLP, GMP and regulatory requirements. Ensure compliance to site and divisional policies and procedures. Support continuous improvement activities. Adhere to Health and Safety within the working environment, highlight opportunities for improvement to EHS performance.
**Main Responsibilities**
+ Perform a variety of sampling activities to support product manufacture in a cGMP regulatory environment.
+ Perform dosimetric analysis, dose map execution and equipment maintenance, accordance with GLP, GMP and ISO 11137.
+ Ensure that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs).
+ Assist in the design and set-up of the site dosimetry lab program.
+ Create and update documentation as needed.
+ Support the set up and maintenance of laboratory equipment and consumables.
+ Ensuring the laboratory is adequately stocked and resourced, with everything accurately labelled.
+ Participate in validation activities as needed for dosimetry lab and equipment qualification program.
+ Review and approval of laboratory test results.
+ Complete records on time and review data for accuracy and completeness.
+ Assist in the identification of root cause analysis and provide technical advice as needed.
+ Support unplanned events and raise out of specification results in a timely manner and inform the Supervisor immediately of any such events.
+ Initiate and complete CAPAs and change controls in accordance with site procedures.
+ Trend data for environmental and product monitoring. This also involves the generation and presentation of quarterly and annual reports
+ Maintain a "right first time" approach to quality records by ensuring accountability for functional responsibilities.
**Qualifications & Experience**
+ Third level Science / Manufacturing or equivalent qualification.
+ Preferred two years' work experience in a Manufacturing / Science / Quality or equivalent environment.
+ Electron beam or other sterilisation technologies experience desirable.
+ Knowledge in ISO 11137 desirable.
+ Chemistry/Microbiology/Dosimetry Lab experience desirable.
**What we Offer:**
Attractive compensation package that includes competitive pay, as well as benefits such as
+ Family health insurance
+ Excellent pension scheme
+ Life assurance
+ Career Development
+ Fantastic new facility
+ Growing business plus access to many more benefits.
Connect with us at and on LinkedIn , Facebook , Instagram , X and YouTube .
Abbott is an equal opportunities employer.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
1
Research Assistant A App Dev for START DS Project Schl of Food Sci & Env H
Dublin, Leinster
Technological University Dublin/TU Dublin
Posted today
Job Viewed
Job Description
Applications invited for the following Post in the Technological University Dublin Post: Research Assistant A App Developer for START DS Project School of Food Science & Environmental Health (Specified purpose for up to 2 years with initial funding for 18 months) Reference: 339/2025 Location: The post will be based at one of the TU Dublin Campuses i.e. Aungier Street, Bolton Street, Grangegorman, Blanchardstown or Tallaght. Regular attendance at other sites will be required. Hours of Work:A 37 hour working week is in operation. Salary: The successful candidate will be appointed at point (01) of the Post-Doctoral Researcher Salary Scale i.e. €32,962 gross per annum. Remuneration may be adjusted from time to time in line with Government pay policy. Incremental credit may apply in line with University policy. Closing Date: 5:00pm on 11th September 2025. Late applications will not be accepted. It is anticipated that interviews for this post will take place in week beginning 6th October 2025. The interview assessment will be 45 minutes in length and will include a presentation of 10 minutes duration. The topic of this presentation will be as follows: Using smartphone-based applications to support adolescent digital wellbeing and engagement in educational settings. What are my skills/past experiences and what I can offer for this topic Application Details/Procedures: For further information and to make an online application for the above post please visit website visit Technological University Dublin is an equal opportunities employer Person Specification TU Dublin is committed to being fully inclusive, which actively recruits, supports and retains staff from all sectors of society. We value diversity as well as celebrate, support and thrive on the contributions of all our employees and the community they represent. We are proud to be an equal opportunities employer and encourage applications from everybody, regardless of race, sex, ethnicity, religion, nationality, sexual orientation, age, disability, gender identity, marital status/civil partnership, pregnancy and maternity, as well as being open to flexible working practices. During the recruitment and section process, candidates will be expected to demonstrate an appropriate mix of knowledge, experience and skills described below. For shortlisting purposes, candidates will be expected to demonstrate the degree to which they meet both the essential and desirable criteria set out below. The ideal candidate will demonstrate the appropriate mix of knowledge, experience, skills, talent and abilities required for the role as outlined below and must satisfy all of the essential criteria: Essential An undergraduate Honours Degree (NQF L8) or equivalent award by an approved degreeawarding Authority in computer science, or related subject Experience in mobile application development (e.g., SWIFT, Flutter, React Native, or Android/iOS native development). Experience with user experience (UX) design or UI prototyping tools (e.g., Figma, Adobe XD). Familiarity with data analysis (e.g., SPSS, R, or Python). Demonstrated familiarity with app development and other related subject matters (e.g. Human-Computer Interaction, Digital Psychology, Educational Technology). Working knowledge of research techniques. Effective written and verbal communication skills. Ability to work independently and collaboratively across international, interdisciplinary teams. Candidates will be shortlisted based on their demonstration of meeting every essential criterion so are asked to clearly outline how their experience and qualifications meet the criteria. Desirable A portfolio of previous development apps. Previous experience working on EU-funded or Erasmus+ projects. Interest in digital wellbeing, education innovation, or social impact tech. Candidates may be shortlisted on the basis of none, one or more of these desirable criteria and are asked to clearly outline how their experience and qualifications meet the criteria. Other requirements for the role Personal attributes required for the role: Strong attention to detail and organisational skills. Demonstrated curiosity and commitment to innovation in education and wellbeing. Proactive communicator who values interdisciplinary collaboration. Commitment to ethical research, especially when working with young people. Further information for Post-doctoral Researcher In the case of a 1st Post-doctoral Fellowship where the applicant may not have graduated yet, the successful applicant must, at the time of appointment, provide a letter from the appropriate graduate studies office confirming that the student has completed the programme including all the examination requirements and is just awaiting the formal graduation ceremony and the likely date on which that will take place. Skills: Research Communication
This advertiser has chosen not to accept applicants from your region.
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