Find Senior manufacturing specialist Jobs in Ireland

Stability Specialist
Vantive —Castlebar, County Mayo
- Doctoral degree
- Word processing
- Master's degree
Lead Supply Chain & Planning Specialist (Functional) - Oracle Fusion
Dexcom —Athenry, County Galway
- Full-time
- Oracle
- Doctoral degree
- ERP systems
Senior OpEx Specialist
WuXi Biologics —Dundalk, County Louth
- Engineering
- Master's degree
- Bachelor's degree
Command Centre Portfolio & Operations Lead
Teleflex —Athlone, County Westmeath
- Oracle
- ERP systems
- Microsoft Office
13d
Senior Specialist - Industry 4.0 & Manufacturing Data
Deep DSG —Cork, County Cork
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- SQL
- Annual leave
- Life insurance
Quick apply
8d
Manufacturing Materials Specialist
WuXi Biologics —Dundalk, County Louth
- Doctoral degree
- Master's degree
- Presentation skills
5d
Sr Quality Systems Eng, WFD
West Pharmaceutical Services —Waterford, County Waterford
- €63,200–€80,500 a year
- Engineering
- Maintenance
- Supervising experience
Senior Biocompatibility Specialist
Zimmer Biomet —Shannon, County Clare
- Full-time
- Doctoral degree
- Presentation skills
- Manufacturing
- Wellness program
Senior Regulatory Affairs Specialist
Natus Neuro —Gort, County Galway
- Full-time
- Microsoft Outlook
- Communication skills
IT Manager
C&D Foods & Affiliates —Edgeworthstown, County Longford
- Full-time
- Azure
- Computer Science
- ERP systems
Quick apply
Hard Services Lead
Apleona Ireland —Kilkenny, County Kilkenny
- €60,000 a year
- Full-time
- No degree
Quick apply
14d
Project Manager Modular Construction
Castle Group —Gort, County Galway
- €50,000–€65,000 a year
- Full-time
- Microsoft Office
- Project management
- Construction
- Wellness program
- Employee assistance program
Quick apply
7d
Senior Technical Analytical Specialist
AbbVie —Sligo, County Sligo
- Full-time
Senior Quality Complaints Specialist (FTC 8 months)
Takeda Pharmaceutical —Dublin, County Dublin
- €57,800–€79,420 a year
- Full-time
- Bachelor's degree
- Continuous improvement
- In-person
- Fuel card
- Employee assistance program
12d
Site Procurement Senior Specialist
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Spanish
- Continuous improvement
- Communication skills
Manufacturing Systems Specialist
WuXi Biologics —Dundalk, County Louth
- Doctoral degree
- Master's degree
- Presentation skills
5d
Senior Audit and Compliance Specialist
Abbott Laboratories —Galway, County Galway
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Engineering
Engineering and Maintenance Manager
Donohoe Drinks Ltd. —Waterford, County Waterford
- Full-time
- Engineering
- Maintenance
- Project management
- Annual leave
- Employee assistance program
Quick apply
Principal Industrial Designer
Logitech —Cork, County Cork
- Full-time
- CAD
- Bachelor's degree
- In-person
- Work from home
Supply Chain Data and Serialisation Specialist
Evumed Limited - Biopharma and generics —Cork, County Cork
- Full-time
- Hybrid work
- Relocation assistance
- Sick pay
Quick apply

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Stability Specialist

Vantive -
Castlebar, County Mayo

Apply Now

Job details

Permanent

Benefits

Company pension
Private medical insurance

Qualifications

Doctoral degree
Word processing
Master's degree
Bachelor's degree
Technical writing
Computer skills
Quality systems

Full job description

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 Stability Specialist, 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.

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 defence 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 required:

Bachelor’s Degree, Master’s or PhD with 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 Vantive can offer to you:

A permanent contract with 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.

Apply Now

Refine Your Search

senior manufacturing specialist jobs in ireland

Stability Specialist

Lead Supply Chain & Planning Specialist (Functional) - Oracle Fusion

Senior OpEx Specialist

Command Centre Portfolio & Operations Lead

Senior Specialist - Industry 4.0 & Manufacturing Data

Manufacturing Materials Specialist

Sr Quality Systems Eng, WFD

Senior Biocompatibility Specialist

Senior Regulatory Affairs Specialist

IT Manager

Hard Services Lead

Project Manager Modular Construction

Senior Technical Analytical Specialist

Senior Quality Complaints Specialist (FTC 8 months)

Site Procurement Senior Specialist

Manufacturing Systems Specialist

Senior Audit and Compliance Specialist

Engineering and Maintenance Manager

Principal Industrial Designer

Supply Chain Data and Serialisation Specialist

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