Senior Specialist Drug Substance Transversal Business Operations
Il y a 3 mois
Job purpose:
The Drug Substance Senior specialist transversal Business operations will be responsible for:
·Training Management for the global Drug Substance organization
·Drive the translation of requirements (EHS, Quality, Finance, Knowledge Management & Risk Management) into fit for purpose DS business processes and the implementation and maintenance of the DS business processes
·Support DS Development Operations & Strategy Head in different continuous improvement initiatives aiming to optimize DS ways of working in various areas, and contribute to implementation across the organization
·Interact with multiple stakeholders across different sites and functions of DS organization and non-DS stakeholders
·Interact closely with TRD function strategy & capability leads and Lab Operations organization
·Drug Substance reference person for non project related topics (infrastructure, facilities,...)
Your responsibilities:
· You are the trainer Manager for the global Drug Substance organisation in close collaboration with the global and local Drug Substance Managers and the Written Standard Team incl the implementation of Drug Substance training strategy, management of functional and role specific Drug Substance training curricula. Participating to improvement projects for training management.
·You define and implement the Drug Substance document management strategy aligned with Technical R&D best practices. You lead monthly Drug Substance Knowledge Management Core team. Point of contact for Knowledge Management for the Drug Substance organisation.
·You are responsible for Operational Risk and Issue management for the global Drug Substance organisation.
·You translate requirements (Quality, EHS, Procurement,..) into fit for purpose DS processes.
·You collect feedback on DS business processes and tools, identify opportunities for improvement and actively contribute to the implementation and maintenance of agreed DS business processes, tools and improvements.
·You manage the operational EHS and Quality topics for Drug Substance (incl follow up Management Monitoring, DS Position papers, review of relevant SOP, leading DS BE EHS forum, setup of the DS risk universe and L1 audit plan, preparation of and participation to IBM and A&A audits,..)
·You generate relevant Quality, EHS, Finance kpi to support performance discussion/decision making at DS quality, EHS or other relevant meetings.
·You represent Drug Substance in different communities of Practices in areas of responsibilities
· You interact with the Lab Operations team (EHS, facilities,..), Q4RD partner, EHS managers and other non DS stakeholders
·You are the Drug Substance go-to person for non project related operational questions (a.o. facilities, infrastructure).
Basic Qualifications:
·Master in Biological sciences education with project management experience (Biotechnology, Molecular Biology, Bio-engineering, Biomedical experience) And/or Project management, Business management & transformation, operational excellence education with scientific experience.
·At least 4 to 5 years of experience in vaccines, biopharmaceuticals or scientific environment.
·Proven Experience in Pharma R&D environment.
·At least 2 years in a managerial role covering various business aspects.
·Experience in Project management.
·Good understanding of Biopharma / vaccine development processes and biomanufacturing.
·Proof of Business skills.
·Understanding GSP and GMP practices & requirements.
·Understanding of Quality (a.o; QMS, QA/QC).
·Good knowledge of EHS (Environment, Health & safety).
·Good stakeholder management and excellent communication skills.
·Strong critical thinking & decision making.
·Fluent in spoken and written English/french both scientifically/technically as well as conversational.
·Open minded & collaborative approach.
·Ability to drive change.
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 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.
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.
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