Fda Jobs in Dunboyne

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QA Validation  

Claran Consultants Ltd - Dublin

strategies Ensure all CQV activities are conducted in compliance with GMP, FDA, EMA, and other applicable regulatory standards. Support the qualification of analytical instruments in accordance with regulatory

from: irishjobs.ie - 16 days ago

Electronic Engineering  

Life Science Recruitment Ltd - Dublin

. 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 your application 55000.0

from: irishjobs.ie - 23 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

CQV Engineer  

PM Group - Dublin

. Responsibilities Field execution of Commissioning, Installation & Operational Qualification (IQ/OQ) Experienced commissioning in grey/black utilities Knowledge of recent regulations (ICH, ASTM, FDA, ISPE) and modern 12000.0

from: irishjobs.ie - 23 days ago

R&D Formulation Chemist  

Life Science Recruitment Ltd - Dublin

formulation shelf-life. Ensure formulations meet regulatory requirements (FDA, EMA, ICH) and contribute to the preparation of CMC (Chemistry, Manufacturing, and Controls) documentation. Support scale-up 50000.0

from: irishjobs.ie - 16 days ago

Distribution Centre Manager  

Catalyx - North Dublin

experience in medical device/pharmaceutical environment. Strong knowledge of GMP/GDP/FDA regulatory & Known Consignor, Warehouse housekeeping, Health & Safety. Excellent interpersonal and communication skills

from: my.hirehive.io - More than 30 days ago

Regulatory Affairs Department Head  

Helsinn Birex Pharmaceuticals Ltd - Dublin

pharmaceutical manufacturing plant, Helsinn Birex Pharmaceuticals Ltd (FDA and IMB approved) which has operated at Damastown Industrial Estate, Mulhuddart, since 1997. HBP develops, manufactures and packages 100000.0

from: irishjobs.ie - 18 days ago

Subject Matter Expert (SME) - Chemical API  

PM Group - Dublin

to process facility design and construction is essential. Good appreciation of appropriate Regulatory framework, such as FDA, EMA, ICH Guidelines Find out more about PM Group and our projects. Why PM Group 12000.0

from: irishjobs.ie - 23 days ago

Tech Transfer Lead  

PE Global - Dublin

and procedures, including safety and training. Ensure that the site meets the quality requirements of its customers and applicable regulations (FDA, EU & international standards) with a full understanding of CMC

from: irishjobs.ie - 25 days ago

Contract Development & Mfg Sr Mgr  

Amgen - Dublin

field Preferred Qualifications: 8+ years of experience in protein, API, DS, DP, or packaging manufacturing environment 8+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory 12000.0

from: irishjobs.ie - 28 days ago


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