Qa Manager Biologics

AXEPTA SA
Vaud, CH
Cette offre d'emploi n'est pas disponible dans votre pays.

Yours Responsibilities

  • Serve as the QA expert for assigned biological products.
  • Oversee the quality of assigned Clinical and Commercial CMOs, including compliance and performance monitoring.
  • Manage quality throughout the lifecycle of assigned projects, from development and process / method validation / transfer to registration and commercialization.
  • Make batch disposition decisions after thoroughly reviewing batch documentation.
  • Collaborate with the other departments for batch confirmation and certification in relevant markets.
  • Maintain and control Product Batch records and databases.
  • Manage and approve deviations, OOS, investigations, CAPAs, and Change Controls promptly.
  • Conduct quality reviews of stability data for products under their scope.
  • Establish and maintain Quality and Technical Agreements with assigned Clinical and Commercial CMOs.
  • Support the maintenance of the Quality Management System, focusing on biologics-related SOPs.
  • Perform internal and external audits as a qualified auditor, review and approve responses, and ensure CAPA follow-up with concerned CMOs.
  • Provide QA support to the RA-CMC group for regulatory submissions and follow-ups.
  • Implement Quality Risk Management to identify and mitigate risks related to product quality, safety, and GMP compliance of the assigned CMO.
  • Interpret and implement GMP, general regulatory requirements, and Quality systems regulations in manufacturing.

Your Qualifications :

  • Master's degree in natural or applied sciences (Pharmacy, Chemistry, Biotechnology, Engineering).
  • Minimum 5 years of experience in Quality Operations for pharmaceuticals.
  • Expertise in manufacturing and testing biotechnology products.
  • Experience overseeing Contractor Quality.
  • In-depth knowledge of cGMP and regulatory requirements
  • Proven ability to write technical documents, such as APQR.
  • Track record in project management as a project team member, able to contribute to multiple ongoing projects.
  • Knowledge of technical transfer requirements for Biologics.
  • Strong interpersonal skills.
  • Excellent verbal and written communication skills, with a well-structured communication and presentation ability.
  • Commitment to continuous improvement.
  • Results-oriented, with skills in negotiation, empathy, diplomacy, and common sense.
  • Fluent in written and spoken English (company language).
  • Willing to travel up to 20%.
  • Il y a 23 jours
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