22 of 22 Remote Permanent GMP Jobs

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 ❯

for urgent issues. Education & Qualifications Bachelor's or Master's degree in Engineering, Software Development, Information Technology, or related fields. Certifications are a plus. Additional certifications like ITIL 4, GMP, or Database technologies are advantageous. Travel & Languages Travel up to 10% within Europe, Asia Pacific, and the Americas, including overnight stays. Languages: English required; Portuguese or Spanish is a plus. More ❯

Education & Qualifications A B achelor's/Masters degree in Engineering , Software development, I nformation technology, or a related field. Advanced degrees or certifications are a plus. Itil 4 , GMP or Database technologies i s a plus Travel Requirements Position involve travel up to 10 % of the time, mostly within Europe , Asia Pacific, and Americas. Most trips will include overnight More ❯

Education & Qualifications A B achelor's/Masters degree in Engineering , Software development, I nformation technology, or a related field. Advanced degrees or certifications are a plus. Itil 4 , GMP or Database technologies i s a plus Travel Requirements Position involve travel up to 10 % of the time, mostly within Europe , Asia Pacific, and Americas. Most trips will include overnight More ❯

Education & Qualifications A Masters/B achelor's degree in business , information technology, or a related field. Advanced degrees or certifications are a plus. Itil 4 , Prince 2 or GMP is a plus Travel Requirements Position will involve up to 25% travel , mostly within Europe , Asia Pacific, and Americas. Most trips will include overnight travel . Languages English Portuguese or More ❯

looking for professionals with these required skills to achieve our goals: Degree level qualification (or strong equivalent experience) in an appropriate scientific, technical or engineering discipline. Thorough knowledge of GMP and Regulatory requirementsin a pharmaceutical environment. Thorough operational knowledge of manufacturing unit operations and plant/laboratory equipment Ability to communicate and influence effectively at all levels of the organisation More ❯

ISA 95/88 Good understanding of industry stands communication protocols like OPC, Modbus, Ether TCP/IP, Seri Good to have: Knowledge of Pharma validation process and documentation (GMP/FDA) - Valuable Kepware/Metricon OPC Server knowledge Effective communication and writing skills Don't meet every single requirements? Studies have shown women and people of colour are less More ❯

an award-winning and growing business In addition, you'll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement The 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 ❯

they function reliability and effectively. Key Requirements: Proven experience with the design and development of control systems e.g. PLC, SCADA, DCS, MES, etc. Ideally person would be from a GMP environment (e.g. Pharma, Food, FMCG, Chem, etc.), but not essential Control System experience is ideally with Siemens products Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an 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 ❯

and experience ideally across all digital media channels but in particular paid search. You will have excellent knowledge of bid management and core technology platforms such as Google Analytics, GMP Platform, SA360 for example. Data analysis and an understanding of the strategic application of digital marketing channels will be a strength. More ❯

high-quality, complex projects that drive scientific discovery and technological advancement. Our Client: This company specialises in the design and delivery of highly regulated environments, focusing on laboratories and GMP manufacturing facilities. They pride themselves on understanding the unique challenges of each project, creating efficient workflows that emphasise user safety and well-being. With a commitment to flexibility and adaptability … ensure that their designs meet the evolving needs of their clients from day one. Senior/Principal Architect Responsibilities: Deliver projects from concept to detailed design for laboratories and GMP manufacturing facilities, ensuring adherence to life science standards. Develop layouts for various laboratory classifications and environments, including clean rooms. Communicate complex ideas clearly and effectively to stakeholders, simplifying technical details … Requirements: Registered Architect (RIBA/ARB) with demonstrable experience in the Life Sciences sector. Proven track record of delivering projects from concept to detailed design for both laboratories and GMP manufacturing facilities. Strong understanding of life science standards and facility classifications. Excellent communication and presentation skills, with the ability to convey complex ideas succinctly. Proficient in Autodesk Revit and AutoCAD 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 ❯

systems function reliably and effectively. Required Skills Proven experience with the design and development of control systems e.g. PLC, SCADA, DCS, MES, etc. Ideally person would be from a GMP environment (e.g. Pharma, Food, FMCG, Chem, etc.), but not essential. Control System experience is ideally with Siemens products. Preferred Skills Experience in a GMP environment. Familiarity with Siemens products. More ❯