Vendor Quality Lead Drug Product
UCB
Braine L'alleud, Walloon Brabant, Belgium
6 dagen geleden

Make your mark for patients.

We’re here because we want to build the future and transform patients’ lives for the better.

At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients.

We promote an environment of diversity, openness, and respect where people can make valuable contributions.

An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?

To strengthen our Global Quality Assurance team, based in our hub in Braine l’Alleud, Belgium, we are looking to fill the position of Vendor Quality Lead for Drug Product .

As a UCB Vendor Quality Lead , you will provide leadership and QA expertise in driving strategic and operational Quality Assurance activities associated with Global Vendors (Contract Manufacturing Organizations) engaged in GMP manufacturing activities for UCB Products.

This will be achieved through close working and partnering with UCB Technical Operations, Vendor teams, Global QA teams, other UCB teams and external parties.

As a UCB Vendor Quality Lead , you will contribute by :

  • Being the central QA point of contact for the organization for investigations / deviations / out-of-specifications / audit observations associated with the assigned vendors.
  • Performing the QA review of deviation notifications and change controls, retrieving and collecting supportive information from involved stakeholders (UCB Vendor Team, GQL, CAS, Business) to allow assessment.
  • Managing the key performance indicators (metrics) for key operational QA activities and services associated with the vendors in the defined described tracking tools and track the vendor’s performance
  • Ensuring all Quality agreements are in place and take ownership of agreements for the vendors. Maintaining Quality Agreement with the vendors up to date and performing periodic reviews and update of the agreement in close collaboration with the product GQLs and the vendors.
  • When applicable, being sure that the Annual Product Stability Program is rolled-out and executed at the vendor in accordance with the UCB Stability Program
  • Ensuring the Product Quality Reviews (PQR) are completed by the vendors in a timely manner and as needed, are reviewed within the requested time period.
  • Ensuring that this review is documented and made available in the UCB Controlled Documents System.

  • Participating as QA representative to the recurrent vendor meetings, present issues and resolutions, and drive vendor quality performance through these meetings
  • Monitor and trend vendor performance including tracking of CAPA events and closure
  • Quality Complaints : Being the contact person for the follow-up with vendors for the manufacturing investigation part.
  • When applicable, ensuring that initial receipt, logging of quality complaints into the UCB Complaint System and provision of responses to the complainant are professionally coordinated and managed.

  • If needed, working with the Vendor team and Global Quality Lead to determine the Root cause of issues which may lead to a Technical meeting.
  • Coordinating vendor quality related investigations

  • Participating on ad-hoc basis to the UCB Product Change Control Committees for activities related to the vendors and review change controls as QA stakeholder.
  • Providing expert QA advice, support and management for technical operational QA and general QA matters associated with the vendors
  • Working closely with Corporate QA teams, Technical Operation Teams, Business stakeholders and Affiliates in an effective and efficient way
  • Covering the entire product life cycle from initial commercialization including Technology Transfer / Knowledge transfer, commercial (key raw materials to distribution), product improvements to phase out for the assigned vendors
  • Owning of the QA plans and product resource and capacity overview for activities associated with the assigned vendors
  • Ensuring all relevant documentation are provided to the vendors and implemented (Methods, Specs, Master Batch record)
  • Ensuring review of relevant RA dossier section related to the assigned vendors
  • Having the overview of UCB audit and HA inspections related to the vendors. Tracking and following-up on Audit observation and CAPA plan implementation at the vendor.
  • Being the QA stakeholder for Vendor Risk management.
  • Managing and controlling quality documents related to the vendors in the UCB Controlled Documents System
  • Providing support to customer audits and Health Authority inspections at the vendors, as needed
  • Receiving, coordinating, reviewing and authorizing product reworks and repackaging
  • Being the point of contact for post-release vendor quality issues (supply chain, distribution, etc.)
  • General accountabilities :

  • As required, provide Operational QA support to other vendors
  • Act as substitute for other Vendor Quality Leads in times of absenteeism (e.g. vacation, illness)
  • Work in accordance with UCB HSE and Corporate policy requirements and drive personal training and development activities to meet the needs of the business and professional career development.
  • Interested? For this position you’ll need the following education , experience and skills :

  • Minimum of 5-10 years working experience in pharmaceutical Industry (either production, QA or QC) with at least 3 years operational GMP experience in biologics manufacturing.
  • Registered in Belgium to act as a QP is a distinct advantage.
  • Must be knowledgeable in several areas of the global pharmaceutical industry, including the interpretation and practical application of applicable regulations.
  • Has a deep knowledge of the pharmaceutical industry from a business and technical perspective including manufacturing of sterile products and quality control of Biologicals

  • Experienced in interaction with regulatory bodies and third-party organizations with respect to QA systems and regulatory inspection preparedness
  • Experience in conducting customer / vendor audits and participation in the management of regulatory inspections
  • Must be able to act in most circumstances without direct supervision and handle complex / difficult situations
  • Must be able to effectively interact with and influence senior internal and external personnel on many aspects of project and product related matters
  • Must possess excellent interpersonal, verbal, and written communication skills at all levels internally and externally especially at senior management levels
  • Must be able to fluently communicate in English language (reading, writing, speaking, comprehension when listening)
  • Skilled and experienced in operating across cultures and in a multi-cultural environment
  • Root cause and risk management / assessment skills
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