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The CAPA Process Analyst leads complex quality investigations, ensuring corrective actions are documented and compliant. Requires CAPA systems experience, a Bachelor's in Life Sciences, and ASQ CQA certification. Effective communication and technical writing are essential.

Mechanical Engineer with experience in CAD, SolidWorks, and automation systems. Responsible for designing mechanical components and systems, contributing to R&D teams, and developing cost-effective prototypes. Requires strong problem-solving and analytical skills, along with technical judgement and ...

Role as Site Administrator involves managing office operations, ensuring efficient work environment, and engaging with employees and visitors. Requires strong organizational and communication skills, with experience in event planning. Ideal candidate is proactive, with a focus on employee ...

The Admin Assistant will review and process sales contracts, maintain CRM data, and support auditing efforts within a healthcare setting. The role requires contract administration experience, strong data analysis, and CRM skills.

Looking for a Phlebotomist Floater to perform blood draws and manage specimen preparation across various locations. Requires 5 years of phlebotomy experience, strong phlebotomy skills, leadership abilities, and confidentiality. Must handle complex customer practices and collaborate with multiple ...

The HR Shared Services Rep provides support in HR areas like Benefits, Payroll, and Colleague Relations while managing and improving processes. Key responsibilities include answering inquiries, facilitating training, and collaborating with stakeholders. Requires HR experience, Workday skills, and ...

The QA Technician ensures the quality of pharmaceutical products and manufacturing processes. Key responsibilities include sampling, testing, documentation, and equipment checks. Requires GMP knowledge, bilingual skills, and proficiency in SAP and other systems. Work involves team collaboration in ...

Seeking a Regulatory Affairs Associate with experience in regulatory applications and medical devices. Key responsibilities include authoring PMA supplements, supporting EU MDR updates, and reviewing engineering protocols. Must possess knowledge of FDA PMA and EU MDR regulations. A degree in ...

The Prior Authorization Specialist is responsible for submitting prior authorizations for molecular pathology testing, reviewing clinical documentation, and ensuring coding alignment. The role requires expertise in prior authorization processing, laboratory billing, and healthcare revenue cycles, ...

Seeking a Quality Control Analyst I in the clinical/scientific domain to perform routine and non-routine chemical testing and analyses using analytical instrumentation. Requires lab experience and skills in compendial testing and wet chemistry. Must communicate effectively and contribute to ...