QC Scheduler

Cpl in partnership with our client Pfizer are seeking a QC Equipment Validation specialist to join the team for an 11 month fixed term contract in their state of the art Dublin, Grange Castle Site. Job Purpose:This position is to provide support to Quality Control with instrument and equipment, Data Integrity, validation, and system administration.This job...

Cpl in partnership with our client Pfizer are seeking a QC Equipment Validation specialist to join the team for an 11 month fixed term contract in their state of the art Dublin, Grange Castle Site. Job Purpose:This position is to provide support to Quality Control with instrument and equipment, Data Integrity, validation, and system administration.This job...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...

What You'll Be Doing:The QC Supervisor will support the QC Chemistry team, overseeing the operation of a QC testing group by taking a hands-on approach to laboratory operations and supervising a team of analysts. Providing technical support for method validation, method transfer, regulatory updates, and new technology as required.Your Responsibilities:Lead a...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...

This is what you will do: Strong working knowledge of the cGMP QC laboratory environment and laboratory equipment associated with biopharmaceutical analysis. Responsible for providing technical and laboratory support to the QC analysts in Alexion Dublin specifically working with the team as a trouble-shooter Possess the ability to understand and...

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...

This is what you will do: The QC Microbiology Specialist will be responsible for technical and quality oversight for activities within the QC Microbiology Department. The Specialist will provide technical support with regard to method verification. Environmental Monitoring, Utiliities and all other lab based activities. You will be responsible for: ...

Job DescriptionThe QC Analyst is responsible for conduction raw material, in process, finished product, and stability testing according to relevant SOPs and in adherence to the site production schedule and for accurately completing all documentation that supports testing procedures. The QC Analyst identifies issues related to laboratory testing and equipment...

Reporting to the QC Supervisor, the role is pivotal in conducting comprehensive chemical analysis, ensuring compliance with cGMP, SOPs, and maintaining Bimeda quality standards. Exceptional attention to detail and a drive for efficiency will be required, with a consistent and accurate approach to testing and documentation whilst adhering to all aspects of...

Reporting to the QC Supervisor, the role is pivotal in conducting comprehensive chemical analysis, ensuring compliance with cGMP, SOPs, and maintaining Bimeda quality standards. Exceptional attention to detail and a drive for efficiency will be required, with a consistent and accurate approach to testing and documentation whilst adhering to all aspects of...

QC Raw Materials and Compendial Associate DirectorAQC Raw Materials and Compendial Associate Director is required to join a Global Biologics organisation on a permanent basis. This is a permanent role offering you the opportunity to work on a state of the art facility. As QC Raw Materials and Compendial Associate Director you will be responsible for ensuring...

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...

QC Instrumentation Maintenance Specialist Industry Pharma/Biotech/Clinical Research Work Experience 1-3 years City Dublin State/Province Dublin Country Ireland Job Description bout PSC Biotech Who we are?PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India,...

Industry Pharma/Biotech/Clinical Research Work Experience 1-3 years City Dublin State/Province Dublin Country Ireland Job Description About PSC Biotech Who we are?PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving...

Industry Pharma/Biotech/Clinical Research Work Experience 1-3 years City Dublin State/Province Dublin Country Ireland Job Description About PSC Biotech Ltd Who we are? PSC Biotech is aleading Biotech Consultancy firm founded in 1996, headquartered in Pomona,California, USA, with Global operations in Ireland, India, Singapore, Australiaand the US,...

ref. 01199QC – Microbiology SpecialistMaternity leave cover opportunity for a Microbiology Senior Technical Specialist with our client, a Biopharma leading company based in County Meath.You'll be responsible for orchestrating, planning, and managing the daily functions of the laboratory alongside coordinating Microbiology validation tasks. Your role...

This is what you will do: The QC Senior Microbiology Analyst will support the Bulk Drug Facility in Dublin with emphasis on microbiological testing such as Environmental Monitoring, Water sampling, TOC, Bioburden and Endotoxin. You will be responsible for: Environmental and Facilities monitoring sampling and testing. Ensuring high cGMP, GLP...