We are seeking an Automation Engineer to join a Medical Device client of ours for a 12 month contract. This role requires expertise in automation technology, process engineering, and an understanding of regulatory standards to ensure that automation systems enhance the efficiency, quality, and compliance of our manufacturing processes. Key Responsibilities: Develop and implement automation [&he...
Read moreOur Pharmaceutical client are seeking skilled and detail-oriented Automation Engineer to join our dynamic engineering team. The ideal candidate will be responsible for maintaining automated systems and processes to optimize efficiency, improve product quality, and reduce operational costs. Responsibilities: Design, implement, and maintain automation systems and solutions across various departme...
Read moreJob Title: CSV Engineer (Computer Systems Validation) Location: Ireland Reports To: Project Manager/ CSV Our client is a leading medical device company dedicated to improving patient care through innovative technology and high-quality products. The CSV Engineer will play a key role in ensuring that all computer systems used in the development, manufacturing, and quality control of medical devic...
Read moreFREELANCE CLINICAL OVERSIGHT MONTIOR JAPAN 12 MONTH CONTRACT Currently, I am partnered with a Global Biopharma Company based in the USA, who are well funded and have global programs. My client is looking for a FREELANCE CLINICAL OVERSIGHT MONITOR to support them across the JAPAN region. Responsibilities Leading sponsor activities across the Japan region ensuring […]
Read moreSummary Responsible Person for the maintenance of applicable Operational Licenses. Responsible for the implementation and maintenance of Quality Management System required as per local regulations and standards. The Responsible Person is the main contact for Quality Assurance (QA) topics to distributors and external bodies (e.g. Swissmedic, Cantonal Pharmacist). Responsibilities To ensure Quali...
Read moreMy client is looking for an energic consultant with a technical scientific background and initial (at least 2 years) experience in GMP/ GDP area (Packaging Labelling, Quality Operations and or Quality System) for a contracted role till end of the year. Daily Responsibilities Reviewing the Batch Record of the CMO with the intent to ensure […]
Read moreCompany: Series B Clinical Stage Biotech Location: Boston MA Role Overview: Staff Data Scientist My client is seeking a Staff Data Scientist to analyze large datasets and developing methods to identify meaningful patterns from their proprietary database. This role will have a significant impact on early discovery, candidate development, and biomarker identification. The ideal candidate […]
Read moreThe ideal candidate will be responsible for planning, coordinating, and implementing projects within the decided-upon budget, timeline, and scope. They will also effectively monitor and present project updates to relevant stakeholders, clients, or project team members. Responsibilities: Generation, Execution / Approval of Qualification Life Cycle documents from SLIA through to PQ and Fin...
Read moreFREELANCE MEDICAL SCIENCE LIASION GLOBAL MEDTECH & DIAGNOSTICS COMPANY GERMANY, SWITZERLAND, AUSTRIA – DACH REGION 12 MONTH CONTRACT Currently, I am partnered with a MedTech & Diagnostics company based in the DACH region who are well funded. My client is looking for a FREELANCE MEDICAL SCIENCE LIASION/MEDICAL MANAGER to support them across the DACH region. […]
Read moreKey Responsibilities Develop and execute commissioning, qualification, and validation (CQV) protocols for DeltaV automation systems. Ensure that all DeltaV systems are validated according to industry standards and regulatory requirements, including GMP and FDA regulations. Collaborate with cross-functional teams to define automation and validation requirements and develop detailed validation pl...
Read moreDaily Duties: You will plan commissioning/qualification and validation activities and implement them at our customers. To do this, you will create and review the associated documentation. In risk management with a focus on sterile manufacturing processes, you will support the respective departments. You are our first point of contact for computer system validation (CSV). Whenever […]
Read moreYour duties as the CQV Engineer will be: Coordinate and support CQV change management, punch management, and non-conformance management. Manage dashboard and KPI reporting for CQV activities. Provide CQV document/admin training and oversee calibration and maintenance. Act as a Subject Matter Expert, offering expertise and coordination to ensure C&Q activities are completed safely, on schedu...
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