Position: Director of Clinical Research A leading pharmaceutical company is seeking a dynamic and imaginative physician drug developer to lead the clinical development of innovative therapeutics. The role involves driving clinical strategies, overseeing trials, and collaborating across teams to ensure integrated product development. Key Responsibilities: Provide strategic leadership for clinica...
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...
Read moreAbout the job Associate Director Pharmacovigilance Operations Flexibility: Hybrid role, 3 days in office Location: Aachen About the company: A speciality pharmaceutical company with innovative drugs to be used in hospitals with products across the selected European markets with additional products approved in the U.S., the EU/EEA/UK, China and South Korea. About the role: The […]
Read more(Senior) Healthcare Compliance Officer About the Company: This small and rapidly expanding pharmaceutical companies focuses on developing products to treat remarkable unmet medical need. They have established a culture revolving around team-work and patient centricity. They have multiple assets across Phases I-III, and with a recent BLA submission to the FDA they plan to continue […]
Read moreValidation Engineer (Senior) – 12 month & 6 month contracts Onsite position (Western Ireland) – Potential to WFH on ad-hoc basis at discretion of manager. Joining team of approx. 6, reporting to Validation Team Leader. Overview: Coordinate the development & maintenance of validation programs in compliance with applicable regulatory and company requirements. Help direct, impl...
Read moreValidation Engineer (Senior) – 12 month & 6 month contracts Onsite position (Western Ireland) – Potential to WFH on ad-hoc basis at discretion of manager. Joining team of approx. 6, reporting to Validation Team Leader. Overview: Coordinate the development & maintenance of validation programs in compliance with applicable regulatory and company requirements. Help direct, impl...
Read moreThe Company – Scienta is teaming up with a privately held Belgium-based respiratory company focused on the development of combination products. The Company’s pharmaceutical products are poised to change the treatment paradigm in large markets including asthma and COPD. Their products, to be used for pharmaceutical development and approval processes, are innovative as well as […]
Read moreThe Company – Scienta is teaming up with a privately held Belgium-based respiratory company focused on the development of combination products. The Company’s pharmaceutical products are poised to change the treatment paradigm in large markets including asthma and COPD. Their products, to be used for pharmaceutical development and approval processes, are innovative as well as […]
Read moreGlobal Director Clinical Strategy About the Company: This medium sized pharmaceutical company already has three commercialised products, with more coming in the pipeline. The company has focused their efforts on providing products first-of-its-kind products to address previously unmet medical needs. Every member of the team is driven by the knowledge their efforts are providing highly […]
Read moreLocation: Cambridge, Massachusetts, US This role is only open to candidates that already have the right to work in the US. No sponsorship available. The Company We are partnered with a leading global biopharma company that is transforming the lives of patients with rare disease through a novel class of medicines. Having delivered the world’s […]
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