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Head of Technical Service – PS/MMC
전망: 140
갱신일: 26-11-2025
위치: Wavre Walloon Brabant
범주: 품질 보증 / 품질 관리 생산/조작 첨단 기술
직업 종류: Full-time
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작업 내용
Be You’ at GSKAt GSK, we’re a company with a purpose to help people do more, feel better and live longer.
We will be delighted to hear from talented individuals that align to our values. These are at the heart of everything we do and include: Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork.
When you set out on your adventure at GSK, we make a deal. You commit to living our values and expectations and performing against our Innovation, Performance and Trust priorities. In return, GSK commits to providing the right environment for you to thrive.
As a modern employer, we empower you to be yourself, share ideas and work collaboratively
Head of Technical Service – PS/MMC
Leads the MPU Local Technical Services Team (65 people) to ensure the availability and performance of plant assets.
Un-interrupted and efficient supply of utilities and functioning of production and infrastructure equipment, manages process engineering projects (up to 250 K€), SMR and maintains and improves equipment and installation of the Manufacturing Performance Unit to achieve optimal efficiency and effectiveness.
Is as a member of the MPU leadership team co-responsible for the MPU results and ensures personal and team objectives are aligned with MPU, Belgium Industrial Operations and GIO goals and objectives
The MPU PSMMC is a Primary MPU composed on 2 manufacturing buildings. WN26.1 being the only Shingrix bulk production building in the GSK Vx network. The second production building is WN17 where the Cervarix bulk production has recently been transferred and which has been chosen for the commercial launch of our new commercial vaccine: RSV. PSMMC is an MPU where routine production at a high rate is combined with large projects with a major impact on the Belgian site.
In this role you will…
Leadership
- As a member of the MPU Leadership Team, contributes to the determination of the MPU manufacturing and supply strategy to meet the business objectives of GSK Vaccines and to secure the overall interests of the company and the welfare of employees.
- Partners with peers and stakeholders in the MPU, above MPU, Shared Services and Centers of Excellence to share vision and work towards common objectives.
- Manages and supervises the day to day preventive and curative maintenance and re-qualification within the Manufacturing Production Unit to secure production.
- Develops and manages cost-effective and adequate maintenance and improvement plans for equipment and installation of the MPU.
- Identifies potential improvements of the current processes while assuring compliance with the Change Management procedures.
- Manages operational improvement projects (development, implementation, validation, revamping)
- Provides technical support to direct reports
- Handles contract management of maintenance contracts with procurement and STS.
- Calibration /Qualification Services : Manages and supervises the day to day calibration and re-qualification of a large diversity of installation and equipment
- Is responsible for developing calibration plans for equipment and installation
- Aligns Calibration & Measurement skills and planning with specific needs of the MPU.
- Master data: Maintain and update all the Master Data date in the area of responsibility.
- Energy Management: Measures energy consumption and deploys energy savings project for the MPU
- Reliability
- Manages MPU Engineering CAPEX projects (up to 250 K€) or modification activities (Site PIP and annual Site SMR project budget of approx. 1 M€) from an engineering perspective to align with MPUs business objectives and to achieve optimal efficiency and effectiveness
- Implements shared service engineering guidelines in process engineering activities
- Works closely with the Maintenance & Engineering Community, the Manufacturing Expertise Center of Excellence and the Shared Service Engineering to develop the right level of expertise within the team in order to support the Manufacturing Production Unit efficiently and to be internally recognized as expert in the area of responsibility
- Develops and proposes long and short-term plans to improve technical services activities to enhance the overall performance of the MPU
- Plays a MPU cross-functional role by providing technical support and expertise to the deviation handling process (root causes identification) and CAPA implementation
- Participates in MPU Industrial Excellence Initiatives
- Leads, selects, trains, evaluates, coaches and motivates the team towards the pursuit of technical services and supply excellence and the attainment of Good Manufacturing Practice
- Ensures optimal staffing levels and competencies are in place and ensures the retention, engagement and development of talent within the organization
- As a leader, personally role models and develops the team towards high performance behaviors in line with the leadership framework.
- Engages the team to deliver the GSK Vaccines, GIO and Belgium Industrial Operations Strategy
- Ensures that the facility and equipment are appropriately designed, the staff is well trained, and a good planning and organization is in place to meet production, quality, cost and security targets and to facilitate the transfer of new processes from New Product Introduction.
- Applies or proposes recommended processes and new technologies to the benefit of the process activities, of the MPU and the whole organization.
- Ensures adherence of the technical services to legal constraints, local and international standards, cMP, Regulatory requirements and all GSK Quality Management Systems (QMS) policies and procedures as applicable.
- Ensures constant analysis of technical standards and risks of the MPU in order to secure unrestricted production capabilities at high quality standards
- Is responsible for preparing and meeting the annual budget (Opex, Capex, Headcount), forecast and manpower allocation
- Manages allocated budget and expenses (in particular but not limited to managerial expenses for maintenance, repairs as well as energy costs)
- Analyses write offs and optimizes working capital
- Is responsible for adherence to all safety and EHSS guidelines and procedures as well as compliance with external and internal standards and policies within the framework of maintenance / technical services
- Proactively promotes and prioritizes EHSS compliance. Makes sure that equipment is compliant with the applicable national regulation (electricity, pressure and lifting)
- Ensures contractors / external providers and own team members are well informed about and adhere to external and internal requirements
- Participates to external audits (FDA, WHO, National and European Health Authorities, . . ) as required
Why you?
Qualifications & Skills
- Master degree in engineering (Civil engineer) or Industrial/Agricultural Engineer
- At least 10 years experience in pharmaceutical and/or biotechnology industry (of which at least 5 years in vaccine production)
- At least 5 years experience in industrial maintenance environment
- Relevant experience in engineering/automation/project management
- Proven experience in people management
- Advanced knowledge in biopharmaceutical technologies or equivalent experience.
- Good understanding of various industrial standards
- Knowledge of reliability maintenance, utilities operations, automation, calibration & measurement
- Proven project management experience, experience with contract management and cost benefit analysis
- Fully knowledgeable on cGMP and BPF for biological products.
- Knowledge of culture and purification processes is an asset for Primary
- Fluent in French and English (written and spoken)
Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork in a culture of Innovation, Performance and Trust.
GSK Vaccines - Our Vaccines business has a broad portfolio and innovative pipeline of vaccines to protect people of all ages. We deliver over two million vaccine doses per day to people living in over 160 countries.
For further information, please visit www.gsk.com.
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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마감 시간: 10-01-2026
무료 후보 신청 클릭
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