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LMSAT Scientist Technical manager in the LMSAT P&P Mastery KM / Training
Ver: 155
Día de actualización: 16-11-2025
Ubicación: Wavre Walloon Brabant
Categoría: Seguro de Calidad / Control de Calidad Producción / Operación
Industria: Pharmaceutical Manufacturing
Tipo de empleo: Full-time
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Contenido de trabajo
Site Name: Belgium-WavrePosted Date: May 16 2022
Job Purpose
This role was created to re-inforce the department to drive the knowledge management process to reinforce product & processmanufacturing.
Are you looking for an opportunity to lead some knowledge management projectswithin the safety, quality, planning and budget in a complex and highly regulated environment? If so, this is the role for you.
As LMSAT Scientist technical manager you will manage some knowledge management project but also troubleshooting or complex projects to ensure product & process mastery within MPUs to reach the highest efficiency & technology standards. Your area of influence will be the whole manufacturing process within BelOps. Projects could be linked to knowledge improvements within operation but also for example a new production method, a complex investigation related to production…
Responsibilities
This role will give YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following
- be responsible to lead projects driven by capture and spreading of Product & Process knowledge within Operations
- be responsible to escalade any potential risk, issue related to the project under your responsibilities
- be responsible to write technical documentation (URS, technical reports, PPQ report) when needed
- be responsible to support one or two technical pillars to deliver the strategy endorsed by Be Operation leaders’ team
- be responsible to implement technical solutions or projects
- be Belgium local subject matter expert for area of your expertise
Basic Qualifications
We are looking for professionals with these required skills to achieve our goals:
- Bachelor’s degree
- 2-3 years in pharmaceutical drugs or in vaccines
- At least 2-3 years in relevant Pharmaceutical Product and process area (Manufacturing (production or QC), technical development, Product life cycle technical management)
If you have the following characteristics, it would be a plus:
- Degree in Chemical engineering/Biochemical engineering or life sciences
- Orange belt or equivalent skills demonstrated in previous projects, GMP certificate, Quality by design certification
- Developing and managing teams and driving results in a matrixial environment
- Proven experience in managing projects
- Excellent analytical skills and learning agility
- Excellent communication, facilitation and influencing skills
- Ability to simplify complex processes, applying innovative thinking
- Leadership and ability to lead and drive change, matrix leadership
- Strong business acumen
- Li-GSK
At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we’re making the most significant changes we’ve made to our business in over 20 years. We’re on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands.
With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together – all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive.
Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients – so we deliver what matters better and faster; accountable for impact – with clear ownership of goals and support to succeed; and where we do the right thing. So, if you’re ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together.
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.
Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.
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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Plazo: 31-12-2025
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