Search the 13 jobs at Azzur Group

The Operations Associate II at Azzur Cleanrooms on Demand supports day-to-day operations in a cleanroom facility, ensuring smooth operations and technical support. Responsibilities include shipping, receiving, equipment maintenance, cleanroom support, and assisting with operations management. The role requires working Monday through Friday from 3:00 PM to 11:00 PM.

As a Commissioning Qualification Validation Engineer, responsible for ensuring successful commissioning, qualification, and validation of critical systems including cleanroom equipment. Tasks include leading commissioning activities, developing validation protocols, troubleshooting technical issues, and ensuring compliance with regulatory standards.

As a Commissioning Qualification Validation Engineer (CQV), play a pivotal role in ensuring the successful commissioning, qualification, and validation of critical systems. Responsibilities include commissioning, qualification, validation, documentation, reporting, troubleshooting, compliance assurance. Bachelor's degree in Engineering or Life Sciences required. Experience in commissioning cleanroom systems, knowledge of regulatory requirements, technical expertise in cleanroom systems needed. Strong analytical and problem-solving skills, effective communication skills.

The Project Coordinator will be responsible for managing client requests, coordinating with various departments, handling invoicing and access management, and facilitating effective communication within the organization. This role requires a high level of organization, attention to detail, and the ability to build and maintain relationships with clients and colleagues.

Seeking a highly organized Project Coordinator to manage client requests, drive revenue growth, and coordinate communication and marketing information. Responsible for invoicing, access management, client relationships, and resolving service issues. Requires 4-8 years of experience or BS in biology, chemistry, or physical sciences. Experience in a regulated manufacturing environment in the biotechnology, pharmaceutical, or medical device industry preferred.

Plan, prioritize, execute, and implement analytical assays. Support Quality Control Analytical Method Transfers. Execute test method transfers/validation/verification protocols for various analytical assays. Demonstrated method troubleshooting capability. Experience with wet bench and analytical instrumentation. Knowledge of cGMP compliance and analytical techniques. Strong communication skills.

The Project Engineer at Azzur Group is responsible for executing and managing customer CAPEX and OPEX projects in the Life Sciences industry. They must ensure adherence to project timelines, budgets, and quality standards. The ideal candidate should have a minimum of 2 years of experience in project engineering, strong project management skills, and a solid understanding of GMP regulations.

Responsible for administration of Environmental Monitoring system, OSIsoft PI Data Historian, and Automation Versioning application platform. Manage data logger integration, PLC programming version control, and critical parameter management. Collaborate with stakeholders, lead Automation Projects, and ensure compliance with GMP manufacturing environment standards.

Lead Automation Engineer responsible for developing and implementing automation strategies for biopharmaceutical manufacturing and laboratory operations. Collaborate with teams to identify needs, develop solutions, and ensure compliance with regulatory requirements. Lead troubleshooting efforts, provide technical assistance, and ensure system optimization. Manage automation projects from concept to completion.

Azzur Lab is seeking a Technical Report Specialist to perform administrative duties including drafting reports, data entry, managing inventory, and assisting with office cleaning. High school diploma required. 1 year of administrative experience is necessary. Benefits include flexible PTO, training opportunities, 401(k) match, and medical benefits.

Manage project requirements, write specifications, validate laboratory/manufacturing equipment, lead project teams, communicate with clients, manage project risks, mentor junior engineers.

Responsible for automation and controls support for daily operations, integrating equipment systems, managing version control, and leading automation projects. Must collaborate with stakeholders, develop validation protocols, and have strong communication skills.

The Capital Project Manager will provide strong project management and strategic oversight on client projects in the life sciences industry. They will develop and execute comprehensive project plans, manage project scope, budget, and schedule, and ensure effective communication and collaboration with cross-functional teams. The successful candidate will have 8+ years of experience in capital project management within the life sciences industry, familiarity with commissioning, qualification, and validation processes, and excellent communication skills.