KI-Beschreibung

As a Quality Control Manager in the Chemistry Lab, you will oversee testing activities and ensure compliance with cGMP standards. This role involves managing a collaborative team, guiding training, and maintaining high-quality documentation while promoting safety and efficiency in the lab.

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  Minimum 5 years of work experience in a GMP environment
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  BS or advanced degree in Chemistry, Biochemistry, Pharmacy, or relevant scientific discipline or equivalent
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  Exceptional scientific and practical knowledge of analytical techniques

KI-Beschreibung

In this role, you will ensure the smooth operation of production equipment through preventive and corrective maintenance. You will collaborate with various teams to optimize processes and support new installations.

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  10 years of industrial maintenance experience
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  Strong knowledge in troubleshooting, mechanics, electricity, and pneumatics
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  Ability to analyze and develop solutions to complex problems

KI-Beschreibung

In this role, you will focus on developing quality narratives and embedding Quality by Design principles in clinical trials. You will partner with teams to manage risks, ensure compliance, and drive quality initiatives, all while adapting strategies to meet evolving challenges.

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  Minimum 8+ years QA experience or relevant experience in quality management, biomedical science, clinical development, or regulatory compliance
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  B.S. or M.S. in Chemistry, Biology, Health, Quality related field, or equivalent
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  Demonstrated applied knowledge of ICH/
  GCP, regulatory guidelines, clinical research processes, and Quality Assurance principles

KI-Beschreibung

As the Director, Global Trial Lead, you will oversee the strategic execution of global clinical trials, ensuring high-quality data and compliance while fostering innovation and collaboration across teams. This role involves managing complex projects, mentoring future leaders, and driving operational excellence to support the growth strategy.

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  Minimum 10 years of experience in clinical operations and global project management
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  Experience in leading global clinical trials and programs at the Director level
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  BA/
  BS required

KI-Beschreibung

In this role, you will ensure compliance and operational excellence by managing GMP/GDP documentation, leading risk assessments, and driving continuous improvement initiatives. Your expertise will support training readiness and maintain audit preparedness in supply chain operations.

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  Minimum 5 years of experience in GMP-regulated pharmaceutical or biotech environment
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  Strong knowledge of GMP/
  GDP regulations and quality systems
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  Experience with electronic Quality Management Systems (e.g., Veeva)

KI-Beschreibung

As a Senior RF Design Engineer, you will be at the forefront of developing innovative IoT wireless solutions, focusing on RF design and architecture while ensuring compliance and performance across various applications.

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  Master’s degree in Electronics Engineering or PhD preferred
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  7+ years’ experience in the semiconductor industry or 12+ years for PhD-qualified candidates
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  Experience with EM simulation tools (HFSS, EMX)

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