Drug Product Validation Lead

Manager, Drug Product - Supply Chain Production PlanningManager, Drug Product - Supply Chain Production PlanningApply locations Cruiserath - IE time type Full time posted on Posted Today job requisition id R1589954Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers...

Job Description Interview Report Our client is an exciting, rapid growing publicly listed clinical stage biopharmaceutical business focussed on establishing best in class teams across all its functions. In 2021, the company successfully completed an IPO on the Nasdaq. To date, the company has raised $300 million +, and is engaged in a major...

Job Description This is a rare opportunity to join a young, exciting clinical-stage biotechnology company. Our client is focused on the discovery and development of novel therapies, with the potential to fundamentally change the course of progressive, debilitating diseases. 2023 has been a year of highly successful rapid growth in the company. ...

Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...

RequirementsTo be successful in this role, you should have a Science/Engineering Degree and 3 years plus relevant validation experience in a GMP environment. Experience in executing multiple projects and participating on cross-functional project teams is essential.Additionally, you should have organizational skills for concurrent execution of multiple...

The ultimate purpose of technology teams in GxP environments is to serve the evolving needs of the business. We are a specialist provider of consultancy and implementation services for IT infrastructure and data architectures within life science manufacturing. Our role is to be a companion on the road for technology teams to be able to use as a tool at times...

We need a Drug Product Formulation Expert to provide expertise in drug product formulation, supporting new product introductions and process developments.Key Activities:Analyze data trends for all performance aspects of the area.Troubleshoot performance trends.Collaborate with cross-functional teams to drive process improvements.The ideal candidate will have...

Job OverviewOleson is a technology strategy and transformation practice uniquely focused on IT/OT systems in manufacturing operations with a particular strength in regulated life sciences manufacturing. Our team of experts provides strategic advice or specific implementation services to deliver successful projects.We have developed our own knowledge and...

We are seeking a highly skilled Validation and Tech Transfer Specialist to join our team at LSC, Life Science Consultants. As a member of our Quality Assurance department, you will be responsible for developing and implementing validation and tech transfer processes for our clients.About the JobDesign and implement validation and tech transfer protocols for...

Cpl Resources in partnership with Pfizer are seeking a highly skilled Cleaning Validation Expert to join their team for an 11-month fixed-term contract at their state-of-the-art plant in Dublin. The role is a critical enabler of product manufacture, requiring a robust and audit-ready cleaning validation program.The successful candidate will be responsible...

Cpl Resources and Pfizer are seeking a highly skilled Validation Process Engineer to join their team for an 11-month fixed-term contract at their state-of-the-art plant in Dublin. The role is a critical enabler of product manufacture, requiring a robust and audit-ready cleaning validation program.The successful candidate will be responsible for providing...

What will you do The Sr Engineer will drive excellence and innovation in both large and small molecule drug product manufacturing at Amgen Dun Laoghaire. As a key player in our global Process Development organization they will be instrumental in ensuring the highest standards of process performance, while also leading the charge in innovative process...

About the OpportunityThis exciting opportunity is available for an experienced MS&T Bioprocess Engineer with our Life Science Recruitment organization based in Dunboyne.Key Responsibilities:Participating in and leading key technology transfers, supporting clinical and commercial new product introduction projects.Development of strategies for and execution of...

TN Ireland is seeking a highly skilled Process Validation Engineer to join their team.This is an excellent opportunity to work with a dynamic company in the biotechnology industry.Responsibilities include establishing themselves in a product lead role where the majority of input provided will be leading of process performance qualification (PPQ),Provide...

CLEANING VALIDATION SPECIALIST Cpl in partnership with our client Pfizer are seeking a Cleaning Validation Specialist to join the team for an 11 month Fixed term contingent contract at their state of the art plant in Dublin Grange Castle. Job Purpose: Pfizer Grange Castle seeks a Cleaning Validation Specialist to work within the Cleaning Validation Team...

Job RequirementsTo be successful in this role, you'll require:A deep understanding of oral solid dosage products formulation and manufacturing.In-depth knowledge of global regulatory requirements related to design and control, including validation/qualification of pharmaceutical manufacturing/packaging processes.Experience with statistical software for...

Senior Validation Engineer12 month contractOn site CarlowAMC22531Start date ASAPI am looking for an experienced Equipment Validation Engineer to support the transition of a new biomanufacturing facility from project phase to a fully operational manufacturing facility.This role would be suitable for a CQV/lead Engineer with 6+ years experience in Vial and...

Senior Validation Engineer12 month contractOn site CarlowAMC22531Start date ASAPI am looking for an experienced Equipment Validation Engineer to support the transition of a new biomanufacturing facility from project phase to a fully operational manufacturing facility.This role would be suitable for a CQV/lead Engineer with 6+ years experience in Vial and...

Squarespace is a design-driven platform empowering entrepreneurs worldwide to build brands and businesses online. Our suite of products includes websites, domains, ecommerce, marketing tools, and hospitality business management via Tock.Your Key ResponsibilitiesDevelop a shared vision for the Internationalization team, informing medium and long-term strategy...

Cleaning Validation Specialist - Pharmaceuticals - 12 Month Contract - Dublin Are you looking for the chance to join a life changing pharmaceutical organisation in their mission to continuously drive innovation? We are recruiting for a Cleaning Validation Specialist for a 12-month contract based in Dublin. Located 15 minutes from Dublin Airport and...