Fda Jobs in Dunboyne

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AR&D Analytical Chemist New  

CPL Recruitment - Dublin

technical background in chemistry, particularly analytical chemistry. • Ability to work to tight timelines. • Good Troubleshooting skills. • Openness to change, receptive to new ideas. • Knowledge of FDA Negotiable

from: cpljobs.com (+2 sources) - 16 days ago

CQV QA Specialist  

Life Science Consultants (LSC) - Dublin

deviations, change controls, and CAPAs. Ensure Compliance: Monitor adherence to FDA, EMA, and internal quality procedures. Conduct Risk Assessments: Identify and address risks related to systems and processes 100000.0

from: irishjobs.ie - 16 days ago

QC Materials Technical Lead  

Life Science Consultants (LSC) - Dublin

/Preventative Action generation. Participate in and support audits, both internal and external (HPRA/FDA etc.) Act as the primary point of contact for audit discussions relating to sample management. Build 60000.0

from: irishjobs.ie - 15 days ago

BI Analyst (Digitalisation Project) New  

CPL Recruitment - Dublin

is a distinct advantage. · Experience in life science sector, GMP solutions deployment and validation and FDA's regulations for electronic documentation (FDA 21 CFR Part-11) will be a distinct advantage Negotiable

from: cpljobs.com - 24 days ago

Global Head of Regulatory Affairs, Pharmaceuticals  

The Panel Group - Dublin

and challenges in key markets. Provide strategic guidance on regulatory pathways and requirements for diverse international regions (e.g., FDA, EU, Canada, ROW, APAC, LATAM). Oversee the preparation and submission

from: irishjobs.ie - 17 days ago

Electronic Engineer  

Life Science Recruitment Ltd - Dublin

principles (e.g. ISO 9001 or ISO 13485) and/or FDA quality system regulation processes according to 21 CFR part 820 and EU MDR. Does this sound like your next career move? For more info forward 55000.0

from: irishjobs.ie - 20 days ago

QC Instrumental Specialist  

CPL Recruitment - Dublin

of 3 years’ experience working in the pharmaceutical industry is required. Knowledge of quality control operations. Experience of regulatory agency audits and an understanding of laboratory GMP’s FDA Negotiable

from: cpljobs.com (+1 source) - 30 days ago

QC Materials Technical Lead (Sample Management)  

Morgan McKinley - Dublin

in and support audits, both internal and external (HPRA/FDA etc.) Act as the primary point of contact for audit discussions relating to sample management Build and foster strong relationships within the biologics 60000.0

from: irishjobs.ie - 15 days ago

Quality Operations Manager  

Embecta - Dublin

Certification is a bonus). Knowledge of FDA requirements and experience managing FDA audits. Experience with process validation, sterilization, and clean room environments is advantageous. Strong interpersonal 12000.0

from: irishjobs.ie - 22 days ago

Planner New  

CPL Recruitment - Dublin

environment. Experience with ERP systems (e.g., SAP, Oracle, JD Edwards). Familiarity with GMP, FDA, and regulatory requirements in pharma manufacturing. Excellent organizational and time management skills Negotiable

from: cpljobs.com - 29 days ago


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