GCP Quality Specialist
2 weeks ago
Job DescriptionWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on GCP, GLP, and Pharmacovigilance regulations.Key Responsibilities:Support the development and maintenance of quality and compliance infrastructure, including drafting, revising, and implementing policies, SOPs, processes, and best practices.Collaborate with cross-functional teams, including Global Quality, Patient Safety, Regulatory Affairs, and strategic partners, to ensure adherence to GCP, GLP, PV, and applicable regulations.Lead inspection readiness activities across all functions, working closely with inspection teams.Participate in audit and inspection planning and provide support during preparation and on-site inspections.Assist staff with audit and inspection responses as needed.Qualifications & Requirements:8+ years of pharmaceutical experience, ideally in global Quality Assurance or Clinical Development.Extensive knowledge of GCP and GVP, with hands-on experience in global audits and/or inspections.Minimum 2 years of experience in SOP creation and management.Strong communication, collaboration, and organizational skills, with the ability to manage multiple priorities across functions.This is a fantastic opportunity to join a world-leading pharmaceutical organisation, shape global clinical quality systems, and drive excellence and compliance across multiple functionsWe are an equal opportunities Recruitment Business and Agency.We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.www.planet-pharma.com
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GCP Quality Specialist
4 weeks ago
Slough, United Kingdom Planet Pharma Full timeWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
1 week ago
Slough, United Kingdom Planet Pharma Full timeWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
2 weeks ago
Slough, United Kingdom Planet Pharma Full timeWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
2 weeks ago
Slough, Slough, United Kingdom Planet Pharma Full time £60,000 - £90,000 per yearWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
2 weeks ago
Slough, Berkshire, United Kingdom Planet Pharma Full timeWe are seeking an experienced Senior Process Quality Excellence Specialist to support the development, implementation, and maintenance of clinical quality systems within Global Clinical Sciences & Operations. This role ensures that quality and compliance risks are proactively identified and mitigated across clinical study activities, with a strong focus on...
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GCP Quality Specialist
7 days ago
Slough, United Kingdom Planet Pharma Full timeKey Responsibilities:Support the development and maintenance of quality and compliance infrastructure, including drafting, revising, and implementing policies, SOPs, processes, and best practices.Collaborate with cross-functional teams, including Global Quality, Patient Safety, Regulatory Affairs, and strategic partners, to ensure adherence to GCP, GLP, PV,...
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GCP Quality consultants
1 week ago
Slough, United Kingdom MSI Pharma Full timeGet AI-powered advice on this job and more exclusive features. Direct message the job poster from MSI Pharma Senior Recruitment Professional | 29 Years of Senior-Level Staffing Expertise | Empowering CRM Migration & Implementation (Veeva / Salesforce)… Two Contract Opportunities – Quality Management System (QMS) Team 12-month contracts (likely...
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Slough, Slough, United Kingdom MSI Pharma Full time £30,000 - £50,000 per yearTwo Contract Opportunities – Quality Management System (QMS) Team12-month contracts (likely extensions) | Inside IR35 | Hybrid: 2 days per week on-site in SloughA global Biotech organisation is expanding its Quality Management System team and has two openings suited to professionals witharound 3–6 years of experience. These roles are hands-on and...
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Slough, United Kingdom ARM Full timeA multinational biopharmaceutical client in Berkshire is seeking an experienced Senior Process Quality Excellence Specialist. The role entails developing clinical quality systems and ensuring compliance with regulations such as GCP and GLP. Candidates should have over 8 years of pharmaceutical experience and be skilled in SOP writing. This contract position...
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Quality Operations Specialist
1 week ago
Slough, United Kingdom ARM Full timeA leading multinational biopharmaceutical company is seeking a Quality Operations Specialist in Slough. The role involves supporting quality systems and compliance, with a focus on GCP regulations and SOP writing. The ideal candidate has over 8 years of pharmaceutical experience and will work in a hybrid setting, with at least 2 days on site. This is a...
