Job Title: QA Compliance Specialist Location: Indianapolis, IN (Onsite) Experience: 8+ years Contract Duration: 12+ Months Role Overview The QA Compliance Specialist will support and maintain Quality Systems within a GMP-regulated biop...
Job Title: GMP Quality Compliance Lead Location: Indianapolis, IN (Onsite) Experience: 8+ years Contract Duration: 12+ Months Role Overview The GMP Quality Compliance Lead will support and maintain Quality Systems within a GMP-regulate...
Job Title: Principal Mechanical Design Engineer Location: Tarrytown, NY Experience Level: 8 10+ Years Employment Type: 12+ Months Contract Role Overview The Principal Mechanical Design Engineer will lead the design and development of c...
Job Title: Electronics Reliability Engineer I Location: Burlington, MA Experience: 3 - 5 Years Role Overview The Engineer I Product Analysis will support failure analysis activities for long-term implantable biomedical devices within an...
Job Title: Regulatory Submission Specialist Location: Florham Park, NJ (Hybrid) Experience: 5+ Years Duration: 12+ months contract Eligibility: US Citizens or Green Card holders only Job Summary The Regulatory Submission Specialist wi...
Job Title: Mechanical Design Engineer Location: Tarrytown, NY Experience Level: 8 10+ Years Employment Type: 12+ Months Contract Role Overview The Mechanical Design Engineer will lead the design and development of complex mechanical an...
Job Title: Lead Mechanical Engineer Location: Tarrytown, NY Experience Level: 8 10+ Years Employment Type: 12+ Months Contract Role Overview The Lead Mechanical Engineer will lead the design and development of complex mechanical and el...
Job Title: Cleaning Validation SME Location: Raleigh, NC (Onsite) Experience: 7 10 years Role Overview This role supports a New Product Introduction program focused on biologics manufacturing. The work centers on facility modifications...
Job Title: Biomedical Electronics Engineer Location: Burlington, MA Experience: 3 - 5 Years Role Overview The Engineer I Product Analysis will support failure analysis activities for long-term implantable biomedical devices within an el...
Ability to translate regulatory and quality requirements into practical business solutions Experience supporting inspections...