Technical Coordinator - Sterile Manufacturing

Contenuto del lavoro

Make your mark for patients

To strengthen our Injectable Production team, we are looking for a talented colleague to fill the position of: Technical Coordinator – Sterile Manufacturing – Braine L’Alleud.

About The Role

The main goal of this function is to coordinate the maintenance activities within the Sterile Manufacturing in partnership with Technical Services, Engineering, IT and site facilities departments.

It includes preventive maintenance, corrective maintenance, metrology, physical and automation assets upgrades but also the coordination, planification and follow-up of the technical shutdowns.

The work consists to organize and follow up, for equipment and premises, the maintenance, technical support & metrology activities in order to improve equipment reliability and high quality state of premises and to optimize scheduling.

It implies the active participation to small technical projects oriented towards the equipment and premises improvement.

You Will Work With

Your major contacts will be with maintenance, automation, utilities, qualification, health safety & environment, site engineer, quality assurance (internal) and equipment suppliers and construction contractors (external).

What You Will Do

• Be the technical Single Point Of Contact for the Department
• Act as Subject Matter Expert in the edition and review of equipment standard operations instructions
• Coach teams on equipment specificities and proper operation
• Coordinate day-to-day maintenance & repair activities
• Inform Manufacturing users on equipment status and maintenance progress
• Supervise strict application of safety rules before and during technical interventions in partnership with Health Safety and Environment
• Act as planner of the shutdown activities of the department
• Participate to CAPEX investment plan
• Follow-up and analyze maintenance, utilities and supplies expenses to optimize cost
• Propose and define equipment & premises small modifications and upgrades to adapt and improve existing assets
• Act as Subject Matter Expert in the review of commissioning/qualification protocols and reports and tests execution
• Ensure appropriate handover of small technical/engineering projects
• Be involved in the improvement initiatives on the shopfloor
• Review the equipment database in SAP
• Check and monitor (in partnership with technical warehouse) spare parts & consumables inventories and replenishment processes
• Propose (in partnership with Method Department) adjustment of maintenance frequencies and tasks according to forecasted equipment usage
• Edit and follow-up change control documentation and CAPA (preventive and corrective actions) associated to equipment technical modifications
• Work with Quality Assurance and Qualification/Validation departments
• Participate as Subject Matter Expert to technical investigations linked to process/maintenance/metrology deviations

Interested? For this position you’ll need the following education, experience and skills:

• You have a technical master degree
• A previous successful experience in pharmaceutical industry and/or sterile manufacturing environment is a big asset
• A previous successful experience in a technical field is a big asset
• You have a strong background in Electrical and Mechanical engineering
• A practical experience on maintenance management software (example: SAP PM) is a big asset
• Green belt certification is an asset
• You can easily interact with peers and support departments
• You are strongly safety minded
• You are fluent in both French and English

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About Us

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?

At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.