Manufacturing Site IT Head

Vor 2 Tagen

Luterbach, Schweiz TN Switzerland Vollzeit

The Site IT Stakeholder Success Lead will facilitate alignment between IT and an assigned line of business. The Stakeholder Success Lead will be focused on ensuring that stakeholders are succeeding to achieve their goals with the IT system they are provided. To ensure “success” means working closely with stakeholders to understand their business strategy and evolving needs, challenges, opportunities, and associated priorities. And then, to ensure their automation and information needs are properly met by working collaboratively with other members of their functional unit and/or other functional units. Stakeholder Success Leads do not just seek out and then funnel problems or issues to system owners but rather take an active role in helping to solve the problem. In all cases, the primary responsibility of the SSL is ensuring the effective ongoing delivery and customization of IT services to stakeholders.

Stakeholder Success Leads are a critical part of the face of IT. They represent ALL of IT to the stakeholder community they serve.

This role emphasizes outcomes (stakeholder success) as opposed to process (relationship management / partnering). Clearly, partnering and relationship management are important activities but what matters most is that our stakeholders are successful, and this requires a certain mindset and approach to the way in which we work with them. It means looking to solve problems rather than processing demand for system requests. It means going beyond the initial request and understanding what success is for the stakeholder - and looking for the best way to drive that success.

This role will be based in the respective manufacturing site and is a full-time on-site role.

What You’ll Do
  • Effectively facilitate dialogues to identify business issues, challenges and areas of opportunity that can be addressed through technology.
  • Manage business technology priorities for an assigned line of business.
  • Align the IT portfolio and roadmap to the business strategy and objectives.
  • Build detailed understanding of how business processes and outcomes are operationalized through technology.
  • Lead discovery, assessment, and business case development for technology investments and ensure those investments are delivered within financial targets.
  • Capture basic user and functional requirements and key design considerations.
  • Direct IT delivery based on the IT portfolio and business priorities, while ensuring progress is on schedule, within budget, and outcomes are high quality.
  • Ensure smooth execution and clear lines of communication between cross-functional IT teams and business areas impacted.
  • Negotiate and draft effective contracts and agreements with third parties to ensure successful engagement outcomes.
  • Drive adoption of IT standards and solutions and identify opportunities to innovate.
  • Continually refresh personal knowledge of industry trends and developments to improve solutions.
  • Manage IT projects being delivered to stakeholders (when appropriate based on scale, area, applications involved, and resources deployed).
  • Engage and coach people to effectively prioritize work, develop themselves personally and professionally, and ensure they have fulfilling professional experiences.
QualificationsWho You Are

You are an experienced IT professional who has solid manufacturing process knowledge and experience with modules for ERP and Manufacturing Execution Systems. You have a track record of successfully developing and leading a manufacturing IT, automation or quality team. You thrive in a fast-paced, dynamic environment and seek continuous improvement opportunities.

Required Skills
  • BS/BA required in Life Sciences, Engineering, or IT related Discipline. Relevant industry certification or training (if applicable).
  • 12+ years’ experience working and supporting manufacturing applications in IT or engineering within Pharma/Biotech industry.
  • Solid level of expertise in ALL of the following areas: Business Analysis, Business Process Improvement, Process Analysis, Business Case Development, Demand Planning, Requirements Analysis, Requirements Definition and Management, Solution Planning, Stakeholder Relationship Management, Stakeholder Satisfaction Measurement, High Level Design, Agile Methodology, Project Management, Financial Management and Forecasting, Vendor Management, Contract Management.
  • Experience working and managing a large manufacturing site while leveraging global IT and a geographically dispersed systems integration partner to provide and assure 24/7 support. Collaborate with vendors to ensure timely and appropriate service levels while driving productivity and cost improvement without any compromise of service availability for PO&T.
  • Experience working in a Life Sciences regulated environment and strong command of software validation and GxP processes.
  • Experience supporting and managing compliance and internal/external audits.
  • Ability to effectively manage, coach and develop IT team.
Additional Information

Diversity is key for the survival of our ecosystem. I believe it is the single most important factor for a balanced flourishing environment where everyone thrives.” Guy Hadari – Chief Information Officer- Biogen.

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired.

#J-18808-Ljbffr

  • Manufacturing Site IT Head

    Vor 2 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    About This Role The Site IT Stakeholder Success Lead will facilitate alignment between IT and an assigned line of business. The Stakeholder Success Lead will be focused on ensuring that stakeholders are succeeding to achieve their goals with the IT system they are provided. To ensure “success” means working closely with stakeholders to understand...

  • Head of EHS, Solothurn

    Vor 2 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    About This Role The Solothurn manufacturing site is a large-scale biologics drug substance manufacturing site with over 400 Biogen FTEs and a commensurate contract workforce. As the Head of EHS for the site you will be responsible for leading and managing all aspects of Environmental, Health, and Safety programs at the site. This role ensures...

  • Head of EHS, Solothurn, Luterbach

    vor 1 Tag

    Luterbach, Schweiz TN Switzerland Vollzeit

    The Solothurn manufacturing site is a large-scale biologics drug substance manufacturing site with over 400 Biogen FTEs and a commensurate contract workforce. As the Head of EHS for the site you will be responsible for leading and managing all aspects of Environmental, Health, and Safety programs at the site. This role ensures compliance with local,...

  • Supervisor Manufacturing

    vor 1 Woche

    Luterbach, Schweiz Biogen Vollzeit

    Job DescriptionAbout This RoleIn this role, you will be responsible for leading a team of Manufacturing Associates, overseeing daily shift tasks, and ensuring compliance with cGMP standards and safety procedures. You will play a key role in maintaining and revising manufacturing documentation to ensure accuracy and compliance with industry regulations.As a...

  • Manufacturing Supervisor

    Vor 3 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    About This Role In this role, you will lead and oversee a team of Manufacturing Associates, coordinate shift tasks, and ensure a commitment to cGMP compliance and safety procedures. You will play a pivotal role in maintaining updated manufacturing documentation and serve as a system expert, leading technical issue resolution and troubleshooting while...

  • Manufacturing Supervisor

    Vor 2 Tagen

    Luterbach, Schweiz TN Switzerland Vollzeit

    In this role, you will lead and oversee a team of Manufacturing Associates, coordinate shift tasks, and ensure a commitment to cGMP compliance and safety procedures. You will play a pivotal role in maintaining updated manufacturing documentation and serve as a system expert, leading technical issue resolution and troubleshooting while actively representing...

  • Manufacturing Associate II

    Vor 5 Tagen

    Luterbach, Schweiz Randstad Vollzeit

    Jobdescription For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II. General Information: Start date: 01.02.2025 End date: 31.01.2026 Extension: Possible Workplace: Solothurn Workload: 100% Remote/Home office: Not available Job Summary: Performs and documents daily manufacturing operations in a cGMP...

  • Manufacturing Coordinator V

    Vor 6 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    The coordinator V is responsible for supporting / enabling manufacturing activities in regard to Compliance, Documentation, Recipe driven operations, Changeover, Tech transfer, and or Training for day-to-day activity. In addition, the Coordinator V is in charge to represent Manufacturing by participating in intra, cross site alignments and cross functional...

  • Manufacturing Associate II

    vor 2 Wochen

    Luterbach, Schweiz Randstad Vollzeit

    Jobdescription For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II.General Information:Start date: 01.02.2025End date: 31.01.2026Extension: Possible Workplace: Solothurn Workload: 100% Remote/Home office: Not available Job Summary: Performs and documents daily manufacturing operations in a cGMP environment...

  • Manufacturing Associate Iii

    Vor 6 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    **Job Description** About This Role** As a Senior Manufacturing Associate III, your primary role involves Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and...

  • Manufacturing Associate II

    Vor 2 Tagen

    Luterbach, Schweiz Randstad Vollzeit

    JobdescriptionFor our client, an international company in Solothurn, we are looking for a Manufacturing Associate II. General Information: Start date: 01.02.2025 End date: 31.01.2026 Extension: PossibleWorkplace: SolothurnWorkload: 100%Remote/Home office: Not availableJob Summary:Performs and documents daily manufacturing operations in a cGMP environment...

  • Manufacturing Associate Iii

    Vor 2 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    As a Manufacturing Upstream Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards. If you thrive in a...

  • Internship Manufacturing Scientist

    vor 23 Stunden

    Luterbach, Schweiz Biogen Vollzeit

    Job Description **About This Role** Based in the new state-of-the-art Solothurn biologics drug substance manufacturing facility, the Process Sciences Laboratory group within the Manufacturing Sciences (MS) department provides key technical expertise to manufacturing processes at the site. We are looking for an intern for a duration of 6 months to prepare,...

  • Manufacturing Associate II

    vor 1 Woche

    Luterbach, Schweiz Randstad (Schweiz) AG Vollzeit

    For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II.General Information:Start date: 01.02.2025End date: 31.01.2026Extension: PossibleWorkplace: SolothurnWorkload: 100%Remote/Home office: Not availableJob Summary:Performs and documents daily manufacturing operations in a cGMP environment including operation...

  • Manufacturing Associate V

    Vor 6 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    **Company Description** About This Role** As a Manufacturing associate V you'll perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing...

  • Manufacturing Associate III

    Vor 5 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    Job DescriptionAs a Manufacturing Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream or downstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards. If...

  • Manufacturing Associate III

    Vor 2 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    Job Description As a Manufacturing Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream or downstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP...

  • Manufacturing Upstream Associate III

    Vor 2 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    Job Description As a Manufacturing Upstream Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards....

  • Manufacturing Associate III, Luterbach

    Vor 2 Tagen

    Luterbach, Schweiz TN Switzerland Vollzeit

    As a Manufacturing Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream or downstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards. If you thrive in...

  • Manufacturing Associate IV

    Vor 2 Tagen

    Luterbach, Schweiz Biogen Vollzeit

    About This Role As a Manufacturing Associate IV, you'll perform processing steps and manufacturing support activities in our facilities in Luterbach (Solothurn). You will be the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. Your responsibilities include performing and...