LMSAT Senior Scientist Technical Manager in the LMSAT Technology Edge

Jobinhalt

Site Name: Belgium-Wavre

Posted Date: Sep 8 2022

Job Purpose

This role was created to re-inforce the department to lead Technology Edge projects related to product & process robustness, new products introductions & some new technologies.

Are you looking for an opportunity to lead the Technology Edge product & process robustness within 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 the technology projects to ensure product & process mastery within MPUs reach the highest technology standards. Your area of influence will be the whole manufacturing process related to data analytics, digitalization, visualization of data, robotization, process improvement & troubleshooting…

Your 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 support new product introduction with BelOps with close collaboration with TRD,be responsible to lead projects driven by one Technical expertise (Technology Edge, Product & Process Mastery and Troubleshooting / Continuous improvements).
• 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
  

Why you?

Basic Qualifications

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

• PhD, Chemical engineering/Biochemical engineering or life sciences with at least 5 years in relevant Pharmaceutical Product and process area (Manufacturing (production or QC), technical development, Product life cycle technical management
• Green belt or equivalent skills demonstrated in previous projects, GMP certificate, Quality by design certification
• Developing and managing teams and driving results
• Solid understanding of supply chain processes and interfaces in a bio-pharma environment
• Proven experience in managing projects
• Excellent analytical skills and learning agility
• Excellent communication, facilitation and influencing skills
• Leadership and ability to lead and drive change, matrix leadership
• Strong business acumen
  

Preferred Qualifications

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

• Interpersonal and influencing skills
• Ability to simplify complex processes, applying innovative thinking
  

Why 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.

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. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.

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.

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