Site Value Stream Leader (SLT Member)

Posted:
1/29/2026, 7:41:42 PM

Location(s):
Central Hungary, Hungary ⋅ Gödöllő, Central Hungary, Hungary

Experience Level(s):
Senior

Field(s):
Operations & Logistics

Workplace Type:
On-site

Site Value Stream Leader (SLT Member)

The posting period will end on the 15th of February in 2026

Business Introduction:

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.

Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.

We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position summary:

The Site Value Stream Leader provides strategic, managerial, and operational leadership to the full manufacturing organization, ensuring robust, compliant, and efficient production. The role is accountable for meeting customer demand through high-quality, reliable supply, drives continuous improvement in productivity, process robustness, EHS performance, and organizational capability. As a key member of the Site Leadership Team, the role contributes to site-wide strategy, culture, and long-term performance.

Key responsibilities:

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Lead and oversee all value stream operations, ensuring delivery according to cGMP, regulatory expectations, and demand forecasts
  • Drive continuous improvement initiatives focusing on process robustness, quality/compliance, and cost efficiency
  • Select, develop, and lead Production Managers, Supervisors, and operational teams, fostering a strong quality mindset and Operational Excellence culture
  • Ensure permanent inspection readiness and represent manufacturing operations during internal and external audits
  • Strengthen EHS performance and promote a proactive safety culture across production operations
  • Contribute to strategic planning, capacity alignment, and implementation of new systems (e.g., MES) to support reliable long-term supply

Basic Qualifications:

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

  • Proven experience in pharmaceutical manufacturing leadership, preferable within vaccines, biologics, or other highly regulated production environments
  • Strong knowledge of cGMP, quality systems, regulatory expectations, and biological production processes
  • Demonstrated capability in people management and organizational development.
  • Fluent written and spoken English
  • Excellent communication, problem-solving, and decision-making skills

Preferred Qualifications:

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

  • Experience working in complex matrix organizations and in cross-functional collaboration with Quality, Engineering, Logistics, or Global functions
  • Track record of successful audit/inspection preparation and defence
  • Strong influencing skills and ability to drive alignment across diverse stakeholders
  • Experience with implementation of digital or automation systems (e.g., MES)
  • Proactivity, strong prioritization, and performance-oriented mindset

 Work pattern:

  • Full-time on-site leadership position with presence required across production areas
  • Occasional extended-hours availability depending on operational needs, audits, or critical events
  • High visibility role with significant responsibility for people, quality, safety, and business performance

*LI-GSK

Why GSK?

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

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any specific adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected].

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels’.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

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 the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/