21 of 21 Remote GMP Jobs

equipment qualifications, process validations, cleaning validations and computer software validations. Previous experience in root cause, corrective action, preventative action and process improvement. Understanding of ISO 9001, Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP) requirements. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel up to 10% a year. Must have a valid driver's license with More ❯

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive More ❯

in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National Regulatory Authority (AIFA) and is compliant with the FDA More ❯

intermediate product release while maintaining an efficient service in line with customer demands for the release of manufactured batches. Give advice and assistance across site on a range of GMP topics. May be expected to carry out GMP or corrective training. Review and approve documents as the Quality representative such as SOPs and technical reports. Support validation document review and More ❯

EudraLex Volume 4 Annex 11. Experience in developing and executing validation test plans, test scripts, and test cases. Excellent problem-solving, analytical, and risk-assessment skills. Experience within a GMP production environment. Fluency in written and spoken English; Dutch language skills are a plus. Skills: Critical evaluation and interpretation of data. Strong knowledge of pharmaceutical manufacturing processes and quality systems. More ❯

to working in a customer-focused service business. Accuracy and attention to detail. Excellent customer service and communication skills. Good written and arithmetic skills to comply with audits and GMP standards. Understanding of GMP/GLP standards. Ability and confidence to work alone on a customer site without supervision and as part of a multi-disciplined team. BSc or equivalent More ❯

You As Senior/Principal Architect Life Sciences you will have experience in delivering projects from concept to detailed design in the life science sector for both laboratories and GMP manufacturing facilities. You will be part of an enthusiastic and committed team of Architects and Technicians who will deliver high quality output on projects. To be successful you will exhibit More ❯

with global sterilisation vendors to plan and manage process transfers. Write protocols, oversee vendor testing, and analyse data. Lead design reviews and recommend optimal sterilisation procedures. Ensure compliance with GMP practices and regulatory standards. Support regulatory documentation and submission processes. The start date is for ASAP. The initial contract length is for 12 months, with options to extend after. The More ❯

inclusive work environment Self-motivated and proactive with the ability to take ownership of tasks and drive them to completion Good Experience in 3rd party tracking & analytics solutions, including GMP and Adobe Previous client facing media agency experience Knowledge of running Google shopping campaigns Benefits Bountiful Cow is a unique place to work. It's the best of both worlds. More ❯

Understanding of distributed systems concepts. Experience with Python for data processing or image analysis. Background or interest in biology, lab automation, or scientific instrumentation. Any experience with regulated environments (GMP, HIPAA, etc.) Any experience with UI/product design processes and tools (wireframes, mockups, looks-like prototypes, etc.). Why You'll Love Working Here Impact : Your work will directly … complex problems at the intersection of software, hardware, and biology-you'll constantly learn and develop new skills. Autonomy : You'll have the freedom to shape our approach to GMP readiness, with support from a talented cross-disciplinary team. Team : Work with the best engineers and scientists in a collaborative environment where diverse perspectives drive innovation. Salary and Benefits Competitive … re building a team that enjoys moving fast, strives for continuous improvement through learning from mistakes, and is passionate about work that contributes to solving real world problems. No GMP experience? No problem! We want someone who is motivated to deliver an innovative product into a regulated space with creative, efficient solutions. If you're excited about solving interesting problems More ❯

Job summary You will be joining NHSBT at a particularly exciting time as we embark on a journey of change, enhancing our current IT service provision. You will lead the systems testing required to ensure the NHSBT Organ and Tissue More ❯

informatics software applications and the vision for modernization in this space Ability to travel for customer meetings and presentations up to 40% Nice to Have Industry experience with QC, GMP quality content, training management, quality systems processes, or manufacturing Leadership of global Sales teams to drive opportunities with intensity Seasoned at developing and maintaining relationships with executive-level stakeholders Published More ❯

toxicological assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility assessment methodology Basic knowledge of FDA and international medical device regulations/directives and working knowledge of GMP/ISO/GLP guidelines as applied to medical device testing and documentation. Have the ability to work with people and teams in a complex, changing environment and be able More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

plans that can be presented clearly at every level WHAT WE ARE LOOKING FOR Have extensive, relevant programmatic experience (Google Ads (Display/Video), DSPs (e.g. Adform, Tradedesk, DV360), GMP and Analytics Have experience with, and gain a lot of energy from, guiding other people Have experience with the Dutch and/or Nordic publisher landscape Are analytical, flexible and More ❯

solutions. • Expertise in DSPs, SSPs, DMPs, CDPs, ad servers, and programmatic advertising. • Proficiency in AI/ML applications for ad targeting, personalization, and optimization. • Experience with Google Marketing Platform (GMP), Amazon Ads, The Trade Desk, or similar ecosystems. • Strong understanding of cloud architectures (AWS, Azure, GCP) and big data technologies. • Experience with privacy-first advertising (cookieless targeting, identity graphs). More ❯