JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are
Company Description ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good
We are seeking an experienced Regional Engineering Lead UK & Ireland to oversee MEP (Mechanical, Electrical, and Plumbing) engineering delivery across a defined country cluster within our EMEA integrated facilities management portfolio serving a global asset
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
QC Validation & Systems Lead Cheshire £40,000 – £50,000 Pharmaceutical / GMP Laboratory The Role We are seeking an experienced QC Validation & Systems Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment. This senior,
Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description As part of the Thermo Fisher Scientific team, youll discover meaningful work that makes a positive impact on a
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as Quality Assurance Auditor II (Technology Solution Audits Team) and enhance our clinical auditing processes by ensuring regulatory compliance and quality standards. What You’ll Do: Conduct and/or
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as Quality Assurance Auditor II (Technology Solution Audits Team) and enhance our clinical auditing processes by ensuring regulatory compliance and quality standards. What Youll Do:
Automation & CSV Engineer (Permanent) - West Yorkshire Pharmaceutical Manufacturing | High-Tech GMP Environment | Career Growth Opportunity An exciting opportunity is available for an Automation & Computer System Validation (CSV) Engineer to join a highly regulated manufacturing
Company Description ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our
Job Description Plan, conduct, and report GxP audits, including technology focused and computerized systems audits, as applicable, across Pharma, Biotech and Healthcare client base. Deliver consultancy services relating to regulated technologies, including governance models, system oversight, risk assessments, compliance
Adamas Consulting is seeking a qualified professional to plan and conduct GxP audits within the Pharma, Biotech, and Healthcare industries. Responsibilities include delivering consultancy services related to AI/ML regulations, mentoring team members, and supporting clients with
Job Description Plan, conduct, and report GxP audits, including technology focused and computerized systems audits, as applicable, across Pharma, Biotech and Healthcare client base. Deliver consultancy services relating to regulated technologies, including governance models, system oversight, risk assessments, compliance