GSK

Associate Director, External Partnerships, Biologics

Collegeville,United States; Durham,United Kingdom; Stevenage,United Kingdom; Waltham,United Kingdom
  • Salary average
    -YEAR
  • Type of employment
    Full-time

Company

We are a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We prioritise innovation in vaccines and specialty medicines to prevent and treat disease.

Responsibilities

  • **Leading the interactions with key priority external partners **
  • 1. Ensure relationships with high priority external partners are built and maintained. Act as the primary external interface with partners / suppliers who are delivering services globally and across pharmaceutical development and clinical supply, with a scope spanning non-regulated through to GxP services to support the R&D portfolio and ultimate commercialization of assets derived from internal GSK discovery pipeline or through business development deals.
  • 2. Lead the CMC matrix of individuals who interact with high priority external partners including MDS staff who are operationally contracting work; subject matter experts necessary to visit, monitor and assess the work proposed or produced such as MDS technical leads, Regulatory, Quality, EHS; Procurement to build incentivisation into contractual obligations and Third Party Resourcing to report into the framework.
  • 3. Build effective with high priority external partners doing pharmaceutical development and clinical manufacturing at both executive and operational levels. Influence such external leaders to develop capabilities that meet GSK's future needs as well as addressing current expectations.
  • 4. Ensure appropriate monitoring of safety, quality, technical capabilities, and performance at high priority external partners in pharmaceutical development and clinical supply; driving continuous process improvement between GSK and high priority external partners. Responsible for execution of the CMC strategy and keeping teams aligned for successful and timely delivery of agreed objectives.
  • 5. Lead the integration of 2nd party CMC supply chains for assets acquired through in-licensing or whole company acquisitions. The leadership of these activities will be end to end to ensure that all aspects of business as usual activities are covered including contracting, business oversight, data transfer, and any other operational requirements needed. Its not intended that this individual will perform all (or any) of these activities nor would they necessarily 'own' the supplier after integration, rather they would provide the leadership to ensure all related support functions complete their portions of the activity and a smooth transition into GSK's standard ways of working is achieved.
  • **Shape supplier selection and performance assessment **
  • 5. Build close collaboration with key internal partners including SED Program Delivery, MDS External Diligence and Scientific Licensing, CMC leads, MDS technical lines, Procurement, and Third Party Resourcing – with this role acting at a finer level of safety and quality and deeper technical knowledge – and with other GSK business units including EHS, Corporate Regulatory, GSC Technical, Supply and Quality functions to continually optimise how suppliers are managed.
  • 6. Make visible and influence strategically with a range of senior decision makers to ensure GSK makes the right choices on external suppliers and that the capabilities of high priority external partners are well understood. This includes liaising with senior project owners (e.g. CMC Leaders), portfolio owners, platform owners in MDS, and assurers (GSC, MSAT), as well as appropriate engagement at governance.
  • 7. Objectively assess the performance of high priority external partners and feed into wider frameworks for vendor selection, formal assessments of their capability, risk escalation and partnership governance.
  • **Drive the strategic direction for managing high priority external partners of pharmaceutical development and clinical supply activities **
  • 8. Develop and lead implementation of a pharmaceutical development and clinical supply relationship strategy with short, medium and long-term deliverables. Simplify the current interactions with external suppliers and coordinate interactions across multiple business units who need to interact with or assure the activities in the suppliers' facilities both before and during work.
  • 9. Continually survey the external landscape to strengthen knowledge of supplier capabilities and ability to meet GSK expectations. Map and benchmark current suppliers using a variety of lenses including book of business, strength of relationship, unique technical capabilities, technical strength, quality management system, safety record and capabilities versus GSK. Use this insight to influence supplier simplification and supplier selection.

Skills used at work

    Site Name: USA - Pennsylvania - Upper Providence, Durham Blackwell Street, UK - Hertfordshire - Stevenage, Waltham

    Posted Date: May 3 2024

    The Strategic External Development (SED) team is an empowered, innovative, and agile CMC development organization within MDS that will unlock the potential to rapidly deliver an increased number of transformative medicines to patients through exceptional relationships with trusted global partners.

    The primary purpose of this job is to manage oversight of and develop and maintain strong trusted relationships with high priority external partners for MDS, supporting product development and clinical supply of the pharmaceutical portfolio across different modalities and enable accelerated supply of medicines to patients with a focus on the biologics portfolio (eg. Monoclonal antibodies, antibody drug conjugates, sterile drug product presentations). High priority external partners for MDS are third parties that are sole suppliers of a critical MDS business activity for delivery of pipeline, third parties delivering a fully externalised R&D asset of critical or high priority, or third parties that are critical to MDS business continuity.

    The role is crucial to build relationships that ensure continuous improvement of how GSK and our partners work together and is essential for ensuring that the relationships are managed, and issues are appropriately escalated, across the governance framework including interactions with senior leaders of the suppliers to ensure the relationships deliver value to GSK long-term.

    This position establishes and enforces necessary governance needed to minimize the risk across the portfolio of projects/activities executed at the high priority external partners for GSK. Within each relationship both the appropriate quality, safety and technical (scientific and engineering) processes and systems must be in place to ensure delivery to GSK and external standards. This position is also accountable for driving continuous improvement to ensure GSK is getting the most value from the spend with these suppliers.

    Key Responsibilities:

    Leading the interactions with key priority external partners

    1. Ensure relationships with high priority external partners are built and maintained. Act as the primary external interface with partners / suppliers who are delivering services globally and across pharmaceutical development and clinical supply, with a scope spanning non-regulated through to GxP services to support the R&D portfolio and ultimate commercialization of assets derived from internal GSK discovery pipeline or through business development deals.

    2. Lead the CMC matrix of individuals who interact with high priority external partners including MDS staff who are operationally contracting work; subject matter experts necessary to visit, monitor and assess the work proposed or produced such as MDS technical leads, Regulatory, Quality, EHS; Procurement to build incentivisation into contractual obligations and Third Party Resourcing to report into the framework.

    3. Build effective with high priority external partners doing pharmaceutical development and clinical manufacturing at both executive and operational levels. Influence such external leaders to develop capabilities that meet GSK's future needs as well as addressing current expectations.

    4. Ensure appropriate monitoring of safety, quality, technical capabilities, and performance at high priority external partners in pharmaceutical development and clinical supply; driving continuous process improvement between GSK and high priority external partners. Responsible for execution of the CMC strategy and keeping teams aligned for successful and timely delivery of agreed objectives.

    5. Lead the integration of 2nd party CMC supply chains for assets acquired through in-licensing or whole company acquisitions. The leadership of these activities will be end to end to ensure that all aspects of business as usual activities are covered including contracting, business oversight, data transfer, and any other operational requirements needed. Its not intended that this individual will perform all (or any) of these activities nor would they necessarily 'own' the supplier after integration, rather they would provide the leadership to ensure all related support functions complete their portions of the activity and a smooth transition into GSK's standard ways of working is achieved.

    Shape supplier selection and performance assessment

    5. Build close collaboration with key internal partners including SED Program Delivery, MDS External Diligence and Scientific Licensing, CMC leads, MDS technical lines, Procurement, and Third Party Resourcing – with this role acting at a finer level of safety and quality and deeper technical knowledge – and with other GSK business units including EHS, Corporate Regulatory, GSC Technical, Supply and Quality functions to continually optimise how suppliers are managed.

    6. Make visible and influence strategically with a range of senior decision makers to ensure GSK makes the right choices on external suppliers and that the capabilities of high priority external partners are well understood. This includes liaising with senior project owners (e.g. CMC Leaders), portfolio owners, platform owners in MDS, and assurers (GSC, MSAT), as well as appropriate engagement at governance.

    7. Objectively assess the performance of high priority external partners and feed into wider frameworks for vendor selection, formal assessments of their capability, risk escalation and partnership governance.

    Drive the strategic direction for managing high priority external partners of pharmaceutical development and clinical supply activities

    8. Develop and lead implementation of a pharmaceutical development and clinical supply relationship strategy with short, medium and long-term deliverables. Simplify the current interactions with external suppliers and coordinate interactions across multiple business units who need to interact with or assure the activities in the suppliers' facilities both before and during work.

    9. Continually survey the external landscape to strengthen knowledge of supplier capabilities and ability to meet GSK expectations. Map and benchmark current suppliers using a variety of lenses including book of business, strength of relationship, unique technical capabilities, technical strength, quality management system, safety record and capabilities versus GSK. Use this insight to influence supplier simplification and supplier selection.

    Why you?

    Basic Qualifications:

    We are looking for professionals with these required skills to achieve our goals:

    • 5+ years' experience with the Pharmaceutical Industry, ideally in drug development / CMC activities for biologics including, for example, monoclonal antibodies, antibody drug conjugates, and sterile drug product presentations.
    • Experience working with third parties and developing effective relationships
    • Experience of non-regulated, GLP and GMP processes necessary to develop a medicine ready for commercial release and supply to the clinic.

    Preferred Qualifications:

    If you have the following characteristics, it would be a plus:

    • Experience working closely with procurement functions.
    • Ability to effectively communicate (written and verbal) and influence key stakeholders at all levels of the organization both internally and externally.
    • Expansive and visionary thinker to drive strategic vision of the partnerships.
    • Strong relationship builder with negotiation skills
    • Ability to successfully manage a global matrix team.
    • Ability to translate complex concepts into actionable and measurable tasks
    • Thrives in a faced paced environment with potential for significant change

    #LI-GSK

    Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

    Why GSK?

    Uniting science, technology and talent to get ahead of disease together.

    GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

    Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

    If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).

    GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

    Important notice to Employment businesses/ Agencies

    GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

    Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.

    Job posted: May 03, 2024

    Expiration date: May 08, 2024