Loading

5 Biotechnologie Stellen in Orbe gefunden

Diese Jobsuche abonnieren
Bitte ausfüllen
Loading
Mit dem Absenden des Formulars erklären Sie sich mit unseren AGB und der Daten­schutz­erklärung einverstanden.
Bitte überprüfen Sie Ihren E-Mail Account, um die Anmeldung abzuschliessen.
Stellenbenachrichtigung
Loading
Stellenbenachrichtigung
Loading

Jobs nach Städten

Stellen zum Suchbegriff Biotechnologie finden sich auch in folgenden Orten:

Loading

Director, Global Commercial QA Manufacturing

bewerten
Bewertung abgegeben
Director, Global Commercial QA Manufacturing

This position will manage Incyte’s Commercial QA Manufacturing group and is based in our offices in Epalinges.

This role is responsible for the global Quality operations related to the manufacture and testing of all commercial drug substances and drug products, of both chemical and biological origin. He/she will ultimately ensure the compliance of manufacturing with cGMP and registration files.

The position is responsible for driving and coordinating all quality assurance manufacturing activities for New Commercial Product Introduction.

The position is also responsible for implementing a continuous improvement mindset and program across the commercial manufacturing organizations.

The Director Global Commercial QA Manufacturing will be a member of the Quality Management Team. He/She will develop and maintain a strong collaboration with Manufacturing functions as well as external partners.

 

Duties and Responsibilities

The Director Global Commercial QA Manufacturing, will be responsible to:

  • Manage and develop the Incyte Global Commercial QA Manufacturing group

  • Drive the Quality oversight of the commercial products manufacturing globally,

  • Lead and Manage all quality and compliance related aspects associated to Commercial Manufacturing including management of associated changes, deviations, disposition,complaints and CAPA

  • Represent QA Management in Change Review Boards and Material Review Boards

  • Coordinate the transfer of activities from Development QA to Commercial QA groups

  • Oversee for QA, Technical Transfers, Process and Method Validation activities and Continuous Process Verifications

  • Drive resolution of internal and external serious quality issues

  • Ensure Continuous alignment of practices across manufacturing sites for dual sourcing

  • Drive and coordinate all QA manufacturing activities for new Commercial Product Introduction to ensure launch readiness

  • Lead the GMP Contractor Quality Management Program and propose new ways of working to increase effectiveness of Contractors’ Quality Oversight

  • Lead the Technical Quality Agreements Program with CMOs

  • Manage the Quality and Business Reviews Program with CMOs to ensure sustained compliance and performance

  • Ensure inspection readiness across Incyte CMOs for product related inspections

  • Assess CMO’s Quality risk levels and ensure risks’ mitigation

  • Perform audits according to the Global Audit Program

  • Organize, drive and monitor execution of strategic Quality Manufacturing initiatives

  • Ensure Commercial QA Manufacturing set of SOPs is maintained and remains state of the art for compliance and efficiency

  • Develop and monitor Quality Metrics pertaining to Product Manufacturing and CMO compliance

  • Deputy of Senior Director Global Commercial QA

  • Performs all responsibilities in accordance with company policies, procedures, applicable regulations and safety requirements

  • Stay current with the applicable regulations and promote Quality across the Incyte organization

Company Culture

  • Contribute positively to a strong culture of business integrity and ethics

  • Act within compliance and legal requirements as well as within company guidelines

Requirements

  • Doctorate or Academic degree in natural or applied sciences (Pharmacy, chemistry, biotechnology, engineering);

  • At least 10 years in QA for international pharmaceutical and/or biotech industry acquired at manufacturing sites and/or overseeing CMOs;

  • Experience in both solid oral dosage forms and biotech/sterile products

  • Thorough knowledge in cGMP and global regulatory requirements (US, EU, JP, CH);

  • Sound awareness and understanding of pharmaceutical and biotech business;

  • Solid experience in team management, with a strong focus on team development;

  • Strong business Mindset with proven ability to strategic thinking

  • Strong Interpersonal skills;

  • Strong verbal and written communication skills with well-structured communication and presentation ability;

  • Results focused which may require negotiating skills, empathy, diplomacy, common sense

  • Project Management Experience

  • English fluency written and spoken (the company language);

  • Travel up to 25%

 

Adresse

Espace des Scienes 13 1400 Yverdon les Bains

Website http://Incyte.com

Yverdon / Epalinges / Yverdon les Bains VD / Yverdon les Bains / Genève

Bewertung hinzufügen

Geben Sie hier Ihre Bewertung für die Firma Incyte ab!

Bewertung abgegeben