Total result: 257
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£14.64 - Hour
Location: Swindon, Wiltshire
... initiatives. What We're Looking For: Experience in a pharmaceutical or regulated GMP environment (MHRA/FDA). Knowledge of cleanroom operations and aseptic processing (preferred). Scientific background (A ...
Company: Adecco
Job type: temporary
(3 weeks ago)
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£65,000 - 69,300 - Annum
Location: Cork, County Cork
... requirements. * Maintain up-to-date knowledge of applicable regulations (e.g., FDA, EU GMP, ISO 14644) and ensure validation activities align with them. * Identify ...
Company: ESS Ltd
Job type: permanent
(3 weeks ago)
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£35,000
Location: Larne
... Interprets, executes and recommends modifications to operating policies where appropriate Be responsible for fulfilling FDA and international regulatory requirements relevant to each project, such as GMP, IDE, PMA, 510 ...
Company: MCS Group
(3 weeks ago)
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£12,000
Location: Limerick, Munster
... of the organisation. Strong knowledge of medical device quality standards ISO13485/FDA practices and GMP or similar regulated industry standards. Proven problem-solving skills ...
Company: Cook Medical
(3 weeks ago)
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£12,000
Location: Dublin, Leinster
... methodologies, with Greenbelt Certification being advantageous. Advanced Technical writing skills are required. Experience with FDA requirements and audits Experience in process validation, sterilization, and cleanroom environments is a ...
Company: embecta
Job type: contract
(3 weeks ago)
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£100,000
Location: Dublin, Leinster
... Actions) Nice to Have Experience in regulated industries (e.g., healthcare compliance: HIPAA, FDA, ISO 13485, IEC 62304) Familiarity with AWS, Azure, or GCP and DevOps practices ...
Company: Capaciteam Limited
(3 weeks ago)
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£12,000
Location: Mayo, Connacht
... including interfacing (preferably POMSnet). Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating ...
Company: Gertek Project Management
(3 weeks ago)
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£12,000
Location: Sligo, Connacht
... including interfacing (preferably POMSnet). Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating ...
Company: Gertek Project Management
(3 weeks ago)
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£100,000
Location: Dublin, Leinster
... Nice to Have: ? Experience working in regulated industries, especially healthcare (e.g., HIPAA, FDA, ISO 13485 and IEC 62304 compliance). ? Familiarity with cloud platforms (AWS, Azure ...
Company: Capaciteam Limited
(3 weeks ago)
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£12,000
Location: Limerick, Munster
... with an ability to deliver process improvement objectives Good knowledge of GMP / FDA regulatory requirements, housekeeping, health and safety. Genuine interest in investing in people and facilitates individual ...
Company: Stryker Ireland
(3 weeks ago)
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£12,000
Location: Cork, Munster
... , equipment reliability metrics, and maintenance planning principles. Good knowledge of GMP / FDA regulatory requirements and current Health and Safety Regulations legislation. Demonstrated ability to lead ...
Company: Stryker Ireland
(3 weeks ago)
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£100,000
Location: Limerick, Munster
... , and regulatory compliance in a GxP environment Strong knowledge of regulatory standards (FDA, EMA, HPRA, etc.) Proficiency in systems like LIMS, MES, ELN, SAP, and DeltaV Proven ...
Company: Life Science Recruitment Ltd
(3 weeks ago)
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£12,000
Location: Limerick, Munster
... , ISO14971, the Medical Device Directive, EU Medical Device Regulation 2017/745 and the FDA QSR including 21 CFR Part 820 and 21 CFR Part 11 ...
Company: Cook Medical
(3 weeks ago)
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£70,000
Location: Louth, Leinster
... and maintenance of the sites facilities systems in line with the relevant auditing (e.g. FDA/HPRA) and safety standards. The Facilities Specialist will own, control and manage the site facilities ...
Company: WuXi Biologics Ireland Limited
(3 weeks ago)
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£150 - 200
... and meeting preparation Represent the Company and Biostatistics function in interactions, both in writing and in person, with the FDA, EMA and other Health Authorities. Supports regulatory submission and interaction, i.e, and IND ...
Company: Asklepios BioPharmaceutical, Inc.
(3 weeks ago)
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£125 - 150
Location: London
... .g., NIST, OWASP, MITRE ATT&CK, PASTA, STRIDE) and standards such as FDA cybersecurity guidance Experience assessing security risks using industry standard methods ...
Company: Cyber Crime
(3 weeks ago)
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£125 - 150
Location: Birmingham
... 95/88 Good to have: Knowledge of Pharma validation process and documentation (GMP / FDA) – Valuable Don’t meet every single requirements? Studies have shown women and people ...
Company: Capgemini Engineering
(3 weeks ago)
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£200 +
Location: London
... , and consistent market growth across almost all indications. Yet there are still only two FDA-approved anti-fibrotic drugs – marketed for lung fibrosis alone – neither of ...
Company: Deep Science Ventures
(3 weeks ago)
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£150 - 200
Location: Reading
... independently in a global, cross-functional environment. Preferred Experience Prior involvement in FDA/EMA submissions. Experience addressing regulatory agency queries. Familiarity with real-world ...
Company: IQVIA
Job type: permanent
(3 weeks ago)
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£200 +
Location: London
... responsible for aligning information security and data protection with our mission to deliver FDA-regulated digital therapeutics. This includes leading regulatory security compliance ... cybersecurity program Own security compliance with HIPAA, 21 CFR Part 11, FDA pre/postmarket cybersecurity guidance, and related frameworks Collaborate with Product, ...
Company: Remepy
(4 weeks ago)
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