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Product quality strategy leader senior director

Rixensart
Gsk Vaccines
Publiée le 18 février
Description de l'offre

Site Name: Belgium-Wavre, Belgium, Belgium-Rixensart, Durham Blackwell Street, France - Evreux, France - Saint-Amand-les-Eaux, Philadelphia Walnut Street, USA - Massachusetts - Boston, USA - Massachusetts - Boston Central, USA - Massachusetts - Boston North, USA - Massachusetts - Boston South, USA - Massachusetts - North Shore, USA - Massachusetts - South Shore, USA - Massachusetts - West Massachusetts, USA - Massachusetts - Worcester, USA - New Jersey - Newark, USA - New Jersey - New Brunswick, USA - New Jersey - New Jersey City, USA - New Jersey - New Milford, USA - New Jersey - North Bergen, USA - New Jersey - Paramus, USA - New Jersey - Paterson, USA - New Jersey - Sewell, USA - New Jersey - South Plainfield, USA - New Jersey - Stirling, USA - New Jersey - Summit, USA - New Jersey - Toms River, USA - New Jersey - Trenton, USA - New Jersey - Union, USA - New Jersey - Vineland, USA - New Jersey - Voorhees, USA - New Jersey - Wayne, USA - New Jersey - Wood Ridge, USA - North Carolina - Durham, USA - Pennsylvania - Pennsylvania Central, USA - Pennsylvania - Pennsylvania East, USA - Pennsylvania - Philadelphia, USA - Pennsylvania - Philadelphia East, USA - Pennsylvania - Philadelphia Metro, USA - Pennsylvania - Philadelphia North

Posted Date: Feb

Product Quality Strategy Leader Senior Director

The posting period will end on the 20th of February in 2026

The role can be done from any location that is close to a GSK location in Europe or in the US

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:

You will lead the Vaccines Product Quality Strategy organization and shape how quality supports our global supply and patient impact. You will work with leaders across Quality, R&D, Supply and Commercial to set strategy, drive risk-based decisions and embed practical improvements. We value strategic thinking, strong influencing skills, and a hands-on approach to improve quality outcomes. This role offers growth, visible impact on global quality plans, and alignment with our mission of uniting science, technology and talent to get ahead of disease together.

Key responsibilities:

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

Define and deploy a clear product quality strategy for Vaccines that aligns with global quality objectives
Lead enterprise-level product quality risk management and governance, including escalations and strategic reviews
Partner with cross-functional leaders to prioritise quality investments, deliverables and continuous improvement programmes
Oversee critical quality metrics, audits and regulatory readiness to maintain supply and compliance
Sponsor digital and data initiatives that simplify quality processes and improve decision making
Build capability and coach teams to embed a proactive, predict-and-prevent quality mindset
Set and translate product quality priorities into clear, measurable plans with timelines and owners
Manage quality governance forums and deliver regular, transparent updates to senior stakeholders
Lead root cause investigations and ensure robust corrective and preventive actions are implemented
Support regulatory inspections and responses, working with operational teams and external authorities when needed
Develop talent, succession plans and inclusive leadership within the quality community

Basic Qualifications:

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

Bachelor's degree in scientific, engineering or related discipline, or equivalent experience
Minimum 10 years' experience in quality, regulatory or manufacturing roles within a regulated healthcare environment
Proven experience in product quality strategy, risk management and governance
Strong experience working with cross-functional and senior stakeholders
Demonstrated record of delivering continuous improvement and change programmes
Fluent in English; good working knowledge of local languages is an advantage

Preferred Qualifications:

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

Advanced degree (MSc, MBA, PhD) in a relevant field
Experience leading quality strategy in biologics, sterile manufacturing, or complex supply networks
Practical experience with regulatory inspections and interactions with major health authorities
Familiarity with digital quality systems, data integrity and automation initiatives
Strong people leadership in a matrix environment, with coaching and talent development experience
Track record of implementing risk-based quality frameworks and measurable KPIs
If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $ to $
If you are based in another US location, the annual base salary range is $ to $

The US salary ranges take into account a number of factors including work location within the US market, the candidate's skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

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.

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.

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