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Johnson & Johnson

Makes prescription drugs and medical devices

Quality Operations Staff - Quality Control

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSukagawa, Fukushima, JapanNo salary listed

About the Job

Requirements

  • Experience in manufacturing, quality assurance/quality control, repair, or maintenance.
  • Experience working under GMP, ISO 13485, or ISO 9001.
  • Experience in design and development work.
  • Business-level English or higher, including participation as Japan's representative in international teleconferences, coordination and negotiation, and English reading, writing, and document preparation.
  • Basic knowledge related to electrical systems.
  • Basic knowledge of the Pharmaceuticals and Medical Devices Act, ISO 13485, or ISO 9001.
  • Ability to investigate and analyze work issues and problems and make improvements from an organization-wide perspective.
  • Basic computer skills, including Word, Excel, Outlook, and PowerPoint.
  • Must be able to commute by car and live within a two-hour one-way drive by local roads.
  • Ability to accept diverse perspectives, take on new challenges and adapt to change.
  • High motivation to learn and improve, and ability to put learning into practice.
  • Ability to build effective relationships with related departments through communication.
  • Interest in developing capabilities in supply chain management, quality management, or project management.
  • Willingness to use logical thinking to continuously improve work efficiency.

Responsibilities

  • Manage incoming inspection of active (electric) medical devices among the site's products and manage the inspection process.
  • Manage and supervise inspection contractors.
  • Coordinate with related domestic and overseas European departments and participate in regular calls.
  • Participate in new product introduction projects and build and improve processes.
  • Create and revise procedures.
  • Prepare for and respond to multiple internal and external quality audits each year.
  • Set short-term departmental strategies and goals, track progress, and manage work.
  • Lead and participate in strategic priority projects for the Sukagawa site and Customer/Commercial Quality.
  • Participate in committees at the Sukagawa site.

Desired Qualifications

  • Experience in industries with stringent GMP requirements, such as pharmaceuticals, medical devices, or cosmetics; experience in electrical manufacturing industries such as automotive or semiconductors is also acceptable.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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