Katerina Alikaridou on LinkedIn: Good morning A few days ago, I visited the production of Mentor Medical… (2024)

🌟#nowhiring 🌟🔍 Position: Equipment Life Cycle Specialist📍 Location: Leiden⏰ Hours: Netherlands, 40h, hybrid way of working Imagine your next role as anEquipment Life Cycle (ELM) Specialistwho has demonstrable experience and affinity with leading equipment introduction projects in a GMP environment. The ideal candidate for this position should have:-Master’s degree or bachelor’s degree (HBO) in Life Sciences or highly experienced in a similar position.-Proven work experience in Pharma with GMP and automation skills.-Proven Project Management skills and experience.To apply for this position or for more information, please click the link below! 👇#engineer#validation#automation#equipment

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#NowHiring in Belgium!Exciting opportunity for an Analytical Chemistry Scientist who specializes in mass spectrometry and will collaborate with the Advanced Material Characterization and Investigations (AMCI) group. 📍 Beerse, Belgium📅 Contract duration: initial 12 months 💻 Working mode: on-site🕒 Working hours: 40 hours per weekInterested? Click 'view job' to learn more and apply now!

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Kudos to you Nikolas Stathonikos for the important work you and your team are doing to advance AI in healthcare. Your commitment and integrity are evident in all your efforts, always aiming to benefit patients and improve clinical practices.#UMCU#pathologie#AI

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🌟 #nowhiring🌟Do you have experience with machinery engineering and equipment validation?Imagine your next role as aValidation Engineer.You will work in full collaboration with the engineering teams as a process technology &equipment validation expert to help deliver solutions to meet the design requirements, quality, and business targets.Ready to make a difference?🔗 click on the link below to Apply#validation#equipment#machineryengineering#manufacturing

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🌟#nowhiring 🌟🔍 Position: Facilities Quality Assurance Engineer 📍 Location: Leiden⏰ Hours: Netherlands, 40h, hybrid way of working Imagine your next role as aFacilitiesQuality Assurance Engineerwho will be responsiblefor supervising and directing all aspects of the operation, maintenance, repairs, and improvements to facilities from a quality expect.You will comply with Good Manufacturing Practices and Safety and Environmental Regulations to ensure execution, compliance, and proper reporting.You will ensure compliance with facilities standards as defined by J&J and External Governmental bodies.To apply for this position or more information, please click the link below! 👇

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🌟 Proud to share that Randstad has developed multiple local and social innovation programs and initiatives to improve employability and promote equal opportunities for migrants and refugees. 🌍✨Please check the links below to learn more relevant information:1. https://lnkd.in/dd8VuzRc.2. https://lnkd.in/dz4Y8eKB#humanforward

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🌟#nowhiring 🌟🔍 Position: Manufacturing Supervisor📍 Location: Leiden⏰ Hours: Netherlands, 40h, on-site & ShiftsImagine your next role as aManufacturing Supervisor. -You will be responsible for achieving and maintaining the production output as documented in the master production schedule or shipment schedule, confirming; safety, cGMP, and lean. You will be working with other manufacturing supervisors. The ideal candidate for this position should have:-Completed HBO education-Relevant work experience in a production environment-Leadership skills-Good knowledge of the Dutch and English language -Business/financial acumen, Six Sigma and process excellence tools/methodologies, presentation skills-Performs pre-determine schedule level checks to ensure quality and reliabilityTo apply for this position or more information, please click the link below! 👇

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🌟 Exciting Opportunity: Technical Specialist🌟📍 Location: Leiden, The Netherlands🕒 Hours: 40h, on-siteJoin our innovative team in Leiden as a Technical Specialist! 🚀 You will actively handle medium and high quality and compliance issues at the lab independently or with the help of the lab technicians. Will work to maintain cGMP compliance and LEAN status of the team. Act as Subject Matter Authority during cGMP inspections and is SPOC (Single Point Of Contact) for the lab during new product implementations, investigations, qualifications, and more.The ideal candidate for this position should have:-Requires strong typing, written, and oral communication skills in English-Ability to work independently as well as collaborate with cross-functional teams to accept challenges and responsibilities-Proven experience with microbiological techniques, such as bioburden, endotoxin, and sterility is preferred.Ready to make a difference? Apply now and become a key player in our journey towards excellence! 🌟🔗 click on the link below to Apply

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