Top Tech Jobs & Startup Jobs in Manchester

As a Manufacturing Engineer II, you'll ensure compliance with safety standards, perform preventive maintenance, troubleshoot equipment, and support continuous improvement in a cleanroom environment.

The Research Physician II role involves overseeing clinical trials, ensuring patient safety, managing study protocols, and complying with regulatory standards. Responsibilities include participant evaluation, recruitment strategy development, and overseeing investigational products while ensuring ethical conduct.

As a Site Specialist, you'll manage stockroom operations, ensure efficient order handling, deliver shipments, and provide customer support while adhering to safety procedures.

The Project Manager will lead multiple projects in Technical Operations, coordinating product introductions and improvements, while ensuring compliance with quality and safety standards.

The Senior Clinical Research Associate monitors clinical trials, ensures compliance with protocols and regulations, and manages communication between stakeholders to enhance trial quality and data accuracy.

As a Clinical Research Associate, you will coordinate clinical monitoring processes, ensuring compliance with regulations and delivering customer service on projects. You will also benefit from award-winning training programs to enhance your skills.

The Clinical Publisher will support the development and publishing of clinical documents, ensuring quality and compliance with regulatory standards while collaborating with cross-functional teams.

The Contracts Specialist III will support the Biosciences Division by drafting, reviewing, and negotiating commercial contracts, while providing legal expertise to enable business growth and manage risks.

The Sr. OEM Sales Representative will manage customer relationships, implement sales strategies, and identify business opportunities while providing sales forecasts and utilizing CRM systems.

The Senior Contract Specialist drafts and negotiates contracts with study sites, ensuring compliance with standards, budget, and risk assessment throughout clinical trials.