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דרושים Assoc Spclst Qual Sys & Compliance ב-Msd ב-Japan, Chiyoda

מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Assoc Spclst Qual Sys & Compliance ב-Japan, Chiyoda והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו Msd. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
חברה (1)
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
Japan
Chiyoda
נמצאו 1 משרות
27.04.2025
MSD

MSD Assoc Spclst Qual Sys & Compliance Japan, Chiyoda

Limitless High-tech career opportunities - Expoint
Supports Regulatory GMP Compliance Inspections of foreign and domestic manufacturers for New Product Applications, Partial Change Applications, and Periodic GMP inspections, including support for remediation of any GMP gaps. Participates...
תיאור:

Job Description

【Main Responsibilities】

Supports new product launch projects and associated Quality & Compliance activities in accordance with established company policies/procedures and applicable governmental regulations:

  • Supports Regulatory GMP Compliance Inspections of foreign and domestic manufacturers for New Product Applications, Partial Change Applications, and Periodic GMP inspections, including support for remediation of any GMP gaps.
  • Participates in cross-functional new product launch projects to support Quality & Compliance activities.
  • In collaboration with Manufacturers and Regulatory functions, manages the Conformance Review Process to evaluate compliance of site practices against the marketing authorizations.
  • Establishes and maintains local procedures for above activities.

In addition, supports the following Quality Assurance activities of the Marketing Authorization Holder:

  • Assures Quality Assurance activities operate within established policies/procedures, global requirements, and all applicable governmental regulations.
  • Establishes and maintains robust local procedures to support implementation of all Quality Assurance activities as defined in the GQP regulations.
  • Critically assess Quality Systems and their implementation to ensure procedures are followed appropriately. Supports the generation of and tracking of CAPAs, as part of the GQP self-inspection process.
  • Drives proactive and continuous improvement of all GQP processes.
  • Performs market release of products including management of the release schedule and ensures a robust release process.
  • Ensures Quality Agreements are in place with all manufacturers and fully meets the intent and requirements of GQP.
  • Coordinates and implements the GQP training program.
  • Supports Computer System Validation activities relating to GQP systems.
  • Ensures Quality Standard Codes for all company products are maintained as current.
  • Supports coordination of any recall activities across a cross-functional team.

Qualification & Experience:

BS Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering (or equivalent) preferred.

Must have strong knowledge of and experience in Quality Assurance and/or Quality Control activities. Must have strong demonstrated communication skills in Japanese and English. Must be knowledgeable of applicable regulations governing operations. Highly motivated individual, with strong interpersonal and leadership skills.

Current Contingent Workers apply


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more
Limitless High-tech career opportunities - Expoint
Supports Regulatory GMP Compliance Inspections of foreign and domestic manufacturers for New Product Applications, Partial Change Applications, and Periodic GMP inspections, including support for remediation of any GMP gaps. Participates...
תיאור:

Job Description

【Main Responsibilities】

Supports new product launch projects and associated Quality & Compliance activities in accordance with established company policies/procedures and applicable governmental regulations:

  • Supports Regulatory GMP Compliance Inspections of foreign and domestic manufacturers for New Product Applications, Partial Change Applications, and Periodic GMP inspections, including support for remediation of any GMP gaps.
  • Participates in cross-functional new product launch projects to support Quality & Compliance activities.
  • In collaboration with Manufacturers and Regulatory functions, manages the Conformance Review Process to evaluate compliance of site practices against the marketing authorizations.
  • Establishes and maintains local procedures for above activities.

In addition, supports the following Quality Assurance activities of the Marketing Authorization Holder:

  • Assures Quality Assurance activities operate within established policies/procedures, global requirements, and all applicable governmental regulations.
  • Establishes and maintains robust local procedures to support implementation of all Quality Assurance activities as defined in the GQP regulations.
  • Critically assess Quality Systems and their implementation to ensure procedures are followed appropriately. Supports the generation of and tracking of CAPAs, as part of the GQP self-inspection process.
  • Drives proactive and continuous improvement of all GQP processes.
  • Performs market release of products including management of the release schedule and ensures a robust release process.
  • Ensures Quality Agreements are in place with all manufacturers and fully meets the intent and requirements of GQP.
  • Coordinates and implements the GQP training program.
  • Supports Computer System Validation activities relating to GQP systems.
  • Ensures Quality Standard Codes for all company products are maintained as current.
  • Supports coordination of any recall activities across a cross-functional team.

Qualification & Experience:

BS Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering (or equivalent) preferred.

Must have strong knowledge of and experience in Quality Assurance and/or Quality Control activities. Must have strong demonstrated communication skills in Japanese and English. Must be knowledgeable of applicable regulations governing operations. Highly motivated individual, with strong interpersonal and leadership skills.

Current Contingent Workers apply


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.


Show more
בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Assoc Spclst Qual Sys & Compliance בחברת Msd ב-Japan, Chiyoda. בין אם אתם מחפשים אתגר חדש ובין אם אתם רוצים לעבוד עם ארגון ספציפי בתפקיד מסוים, Expoint מקלה על מציאת התאמת העבודה המושלמת עבורכם. התחברו לחברות מובילות באזור שלכם עוד היום וקדמו את קריירת ההייטק שלכם! הירשמו היום ועשו את הצעד הבא במסע הקריירה שלכם בעזרת אקספוינט.