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Alcon

Eye care products and vision solutions

Manager – Good Clinical Practices

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time$110.5k - $143k /yr

About the Job

Requirements

  • A bachelor’s degree or equivalent years of directly related experience is required; stated alternatives include high school plus 13 years, an associate degree plus 9 years, a master’s degree plus 2 years, or a PhD with 0 years.
  • Fluency in reading, writing, understanding, and communicating in English is required.
  • Five years of relevant experience is required.

Responsibilities

  • Manage individual projects, applying advanced knowledge to achieve objectives and improve project performance and operational efficiency.
  • Oversee day-to-day operations, ensuring productivity and alignment with departmental objectives.
  • Make operational decisions and manage programs, resources, and schedules.
  • Ensure implementation of quality management systems at every stage of processes and operations.
  • Implement quality assurance regulations and write, revise, review, and approve standard operating procedures.
  • Perform and support inspections and audits of processes and documents associated with studies, facilities, equipment, suppliers, and vendors to ensure compliance with applicable Good Clinical Practice and Good Laboratory Practice regulatory requirements, standard operating procedures, and study protocols.
  • Manage, support, and facilitate internal and external audits and regulatory inspections, ensure site preparedness, and coordinate Corrective and Preventive Action processes.
  • Report potential quality and compliance issues, ineffective processes or procedures, and deviations, and recommend appropriate corrective and preventive actions.
  • Lead implementation of new regulations, regulatory guidance, and international standards.
  • Ensure adherence to Good Practice regulations by following standard operating procedures, maintaining accurate documentation, ensuring rigorous quality, and completing required training.
  • Adhere to regulatory requirements and continuously improve compliance.

Desired Qualifications

  • Knowledge of ISO 14155, ICH E6, medical device EU requirements, FDA regulatory requirements, and the Declaration of Helsinki.
  • A validated Good Clinical Practice audit track record.

About the Company

Alcon

Eye care products and vision solutions

Alcon provides eye care products and vision solutions to improve how people see. It develops and manufactures devices and consumables for eye health, including cataract surgery equipment and intraocular lenses, retinal health therapies, and contact lenses, distributed through eye care professionals, hospitals, and consumers. The products work by supporting eye surgery, protecting and restoring vision, or correcting vision with lens-based options, backed by research and development and a global distribution network. Alcon differentiates itself with a broad, end-to-end portfolio across the eye care continuum, a strong emphasis on research and development, strategic partnerships with healthcare providers, and a commitment to diversity and inclusion. Its goal is to enhance vision and quality of life by delivering reliable, high-quality eye care solutions and advancing the science of eye health.

Company size
10,001+
Company stage
IPO
Headquarters
Geneva, Switzerland
Founded
1945

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