Our 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 moreLocation: Paris, France Company Overview: This is an exciting opportunity to contribute to the expansion and success of a leading health and wellness company. Job Description: In this role, you will be responsible for ensuring regulatory compliance and managing regulatory submissions for the company’s products. Your key responsibilities will include: Verifying the regulatory compliance of [&hel...
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 moreOur Partner We are partnered with a global consulting firm which services the healthcare industry, they have been well established in the global market particularly in the Regulatory affairs services, they have partnered with innovative companies at the forefront of advanced therapies. As part of their double digit % growth they are searching for a […]
Read moreOur Client We are partnered with a leading player in the production of Oleochemicals serving diverse industries such as food, cosmetics, and pharmaceuticals. With a commitment to sustainability and innovation, their tailored solutions, ensure they stay competitive in a dynamic market. The Role Support of the existing customer portfolio from the chemical, cosmetics, food and […]
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 morePosition: Senior 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, collaborating across teams to ensure integrated product development and leading a team. Key Responsibilities Provide strategic l...
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 moreWe are seeking an experienced Automation Engineer (12 month contract) to join our pharmaceutical client in Basel. The ideal candidate will play a key role in designing, developing, and maintaining automated systems used in the manufacturing process. This role is essential for ensuring the highest levels of efficiency, quality, and compliance with industry standards, especially […]
Read morePosition: 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 […]
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