Wolverhampton, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Preston, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Hemel Hempstead, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Swindon, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Portsmouth, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Watford, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Milton Keynes, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Luton, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Sheffield, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Warrington, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Bolton, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Stoke-on-Trent, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Crawley, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Leeds, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
East Horsley, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Hounslow, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Hull, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Newcastle upon Tyne, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
stakeholder expectations Serve as a key liaison between technical teams and business units Regulatory Compliance Lead technology compliance efforts aligned with international standards (e.g., FDA 21 CFR Part 11, GAMP 5, ICH GCP) Conduct internal audits and support external audits from regulatory authorities and partners Drive risk assessments and implement mitigation strategies Maintain and enhance compliance documentation (SOPs, policies, validation More ❯
Liverpool, Merseyside, North West, United Kingdom Hybrid / WFH Options
CRESSIDA CONSULTING LTD
/OQ, cable schedules, I/O lists Electrical panel layouts and schematics using Eplan 8 Collaborating with mechanical, process and EC&I teams Global commissioning, testing and validation (GAMP, FDA, ATEX, SIL) What Youll Bring Degree or HND in Electrical, Automation or similar field Experience in automation and control of complex systems Confident working with Eplan or similar electrical More ❯
implement Siemens automation solutions (PCS7, SIMATIC SCADA, TIA Portal, MES). Program and troubleshoot PLC (S7-1500, S7-1200) and DCS for optimized process control. Ensure compliance with GMP, GAMP, FDA guidelines in automation projects. Oversee commissioning, validation, and maintenance of automation systems. Collaborate with process engineering, IT, and quality teams to enhance automation efficiency. Stay updated on emerging Siemens … Required Technical Skills: 5+ years in pharmaceutical automation with Siemens systems. Strong expertise in PCS7, SCADA, MES, and PLC programming (TIA Portal) . Deep knowledge of regulatory standards (GMP, GAMP, FDA) . Experience managing automation projects, validation, and troubleshooting . More ❯
looking for an experienced IT Business Partner – Testing and Compliance, accountable for providing IT Test Management and ensuring compliance IT delivery and environments to Computer Systems Validation (CSV) and GAMP standards across Healthcare and Specialist Logistics (HSL) operations. WHAT YOU'LL DO Responsibility for coordinating all Test, Release and IT GAMP compliance activity across the UK HSL Pharma sites and More ❯
support within regulated frameworks. Required Skills: 8+ years of experience supporting and maintaining lab systems in a regulated environment. Strong knowledge of system validation lifecycle documentation and compliance frameworks (GAMP, CSV, etc.). Experience integrating lab systems (LIMS, SDMS, ELN, LES) and supporting digital transformation projects. Ability to lead cross-functional collaboration between IT, validation, and business teams. Excellent written More ❯
test plans and test protocols Project delivery reporting Working within a client-led team to deliver a key client project Stakeholder management Experience of working with S88, PCS7 and GAMP 5 Qualifications Candidates must have proven experience of automation delivery on multiple projects in the pharmaceutical industry. Knowledge of industry standards and systems is essential, alongside a good understanding of More ❯
Billingham, Stockton-on-Tees, County Durham, United Kingdom
PM Group
test plans and test protocols Project delivery reporting Working within a client-led team to deliver a key client project Stakeholder management Experience of working with S88, PCS7 and GAMP 5 Qualifications Candidates must have proven experience of automation delivery on multiple projects in the pharmaceutical industry. Knowledge of industry standards and systems is essential, alongside a good understanding of More ❯