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QA/QC Inspector role in Health Care, requiring 0-2 years in quality inspection, preferably in medical devices. Key duties include conducting visual, dimensional, and functional inspections, and recording test data. Must possess skills in optical measurement equipment and sampling techniques. ...

Seeking an Active Ingredient Technician with expertise in virus and cell culture techniques for vaccine preparation. Responsibilities include compliance with SOPs, training staff, and maintaining data accuracy. Must have GMP and clean room experience. Requires strong problem-solving skills and ...

As a QA/QC Inspector, you will inspect final assemblies and ensure quality compliance in manufacturing. Key responsibilities include evaluating finished devices, performing audits, and interfacing with engineers. Competencies required include inspection skills, blueprint reading, and following cGMP ...

As a Quality Engineer, responsible for providing quality oversight and guidance for cGMP work orders. Requires familiarity with pharmaceutical standards and collaboration with various departments. Must possess skills in quality risk management, equipment monitoring, and validation activities. Prior ...

The Clinical Contract Coordinator is responsible for organizing biological specimen management and laboratory operations. Key duties include managing sample operations, ensuring regulatory compliance, and supporting clinical trials. Required competencies include LIMS experience, biospecimen ...

Seeking a Clinical Research Associate with entry-level experience in laboratory settings. Responsibilities include designing research, analyzing data, and performing laboratory calculations. Must have strong organizational and communication skills. B.S. degree in life science required.

Position for Software Quality Engineer with expertise in medical device software validation. Key responsibilities include developing validation plans, designing test cases, implementing test procedures, and analyzing results. Must have experience in FDA/ISO regulated environments and strong ...

The Medical Affairs Associate supports activities related to expanded access programs, coordinating deliverables, managing vendors, and ensuring regulatory alignment. Requires 3-5 years experience in oncology/hematology and study start-up, with skills in clinical study execution and vendor ...

The role of a Formulation Chemist involves conducting formulation development activities with a focus on product launch and regional support for herbicide and fungicide products. Key responsibilities include designing and implementing R&D programs, executing projects, and providing technical ...

The Medical Science Liaison will build relationships with key opinion leaders, provide scientific support, and gather insights. Responsibilities include disseminating scientific information, attending conferences, and managing team operations. Requires advanced scientific degree, strong ...