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Johnson & Johnson

Makes prescription drugs and medical devices

Surgery Commercial Quality Analyst

Regulatory & Quality (Life Sciences)Posted on Nov 10
Full-timeBogotá, Bogota, ColombiaNo salary listedHybrid

About the Job

Requirements

  • A bachelor's degree is required; a degree in science, engineering, chemistry, pharmacy, administration, or a related field is preferred.
  • At least 2 years of work experience in Quality Systems (Good Manufacturing Practices) is required; experience in medical device companies is preferred.
  • English proficiency at a minimum of B1 is required.
  • Knowledge of Microsoft Office is required.
  • Knowledge of SAP and Excel is desirable.
  • Quality System courses are desirable.
  • Strong written and verbal communication skills are required.
  • The role requires management of complexity, planning and organization, prioritization of activities, urgency, teamwork, and results orientation.
  • Good communication skills in English and Spanish are required.

Responsibilities

  • Ensure compliance with company policies, procedures, and quality standards.
  • Support implementation of applicable Quality System requirements, including segment, global, regional, and local requirements.
  • Support investigations of non-conformances, define preventive and corrective actions through root-cause analysis, and participate in meetings with involved areas.
  • Manage the training process, ensuring timely completion metrics and compliance with minimum requirements in the Curriculum Matrix.
  • Support document control and records management processes, ensuring compliance with company procedures.
  • Support Change Control execution, ensuring changes are evaluated, registered, reviewed, and approved before implementation.
  • Manage technovigilance surveillance and report serious and non-serious medical-device adverse events to health authorities as required by Resolution 4816 of 2008.
  • Manage local product discontinuation and new product introduction processes and evaluate Local Opportunity Products (POLO).
  • Interact with manufacturing plants to manage local reconditioning in compliance with company Repack & Relabel requirements.
  • Document non-conformities in the Designated Electronic System (DES), ensuring completion of identification, investigation, cause analysis, correction, corrective and preventive action implementation, and effectiveness verification.
  • Deploy recall, stop-shipment, and sanitary-alert processes as required by Quality Management.
  • Perform material-handling data transactions in SAP Master Data.
  • Manage shipment of product complaint samples to the operating company.
  • Provide backup support for responsibilities assigned under the established backup system; the Commercial Quality Supervisor or Specialist may support activities in this job description when required.
  • Ensure compliance with Good Practices, EHS regulations, and other company policies and guidelines.

Desired Qualifications

  • Experience in a medical device company.
  • Knowledge of SAP and Excel.
  • Quality System courses.

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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