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Production Line Manager

職缺編號
482425
發布時間
23-十月-2025
組織
Siemens Healthineers
工作領域
Manufacturing
公司
Siemens Healthcare Diagnostics Manufacturing Ltd
經驗等級
中級專業人士
工作职位
全職
工作模式
僅辦公室/ 工地
工作性質
長期
地點
  • Sudbury - Suffolk - 英國

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

Apply now for the position of Production Line Manager and be responsible for the safe and effective management of production, ensuring daily and weekly metrics are achieved and exceeded, whilst maintaining Safety and Quality standards at all times. This is a full-time role based at our Sudbury facility.

Your Role:

  • You will be responsible for ensuring compliance with the Health, Safety and Environment statements, policies and procedures as well as ensuring that all H&S audits are carried out accordingly as well as annual assessments.
  • You will be responsible for managing a team with focus on Safety, Quality, Customer Service and Costs ensuring production orders are delivered to achieve due dates thus reducing potential for missed customer orders.
  • You will carry out regular analysis, to optimize capacity plans and to maintain the optimal level of direct staff.
  • You will contribute actively towards reducing year-on-year product cost movements by improving production utilisation & efficiency and ensuring all CI activities are resourced, managed and driven to successful completion.
  • You will ensure that any new products enter manufacturing in a well-planned/optimized manner, and influence product design for ease and consistency of manufacture.
  • You will be responsible for conducting daily, weekly and monthly planning in conjunction with the Demand Planning group to ensure customer orders are being fulfilled on time and identifying with relevant functions where potential issues may arise and escalate accordingly.
  • You will work with functional groups to identify process improvements in documentation/processes (i.e. Quality Notification’s) to ensure compliance.
  • You will demonstrate leadership in strengthening the site continuous improvement culture, coaching and facilitating in the use of core methods such as Structured Problem Solving, Agile Visual Management and Value Stream Mapping.
  • You will assist Support Engineers and Quality group with Validation tasks requiring risk assessments and validation protocols, both the plans and final reports, ensuring all manufacturing activities are undertaken in accordance with the documentation.

Your Expertise:

  • 2 or more years’ experience in a medical manufacturing environment.
  • Experience of low to medium volume manufacturing, manual processes. Zero defect culture. Focus on meeting customer quality & demand requirements.
  • IT literate with strong knowledge of Microsoft Office packages.
  • You will be able to manage time effectively and possess a desire to succeed.
  • You will have a flexible approach and ability to adapt according to workload.
  • You are self motivated, reliable, able to work on own initiative, manage time effectively and possess a desire to succeed.

Our Benefits:

  • 26 days' holiday with the option to buy or sell an additional 5
  • Up to 10% employer pension contribution
  • Share and bonus scheme
  • Access to our flexible benefits from private medical insurance to dental cover
  • Corporate Social Responsibility opportunities including 2 paid volunteering days per year and support from our 24/7 employee assistance programme

Who we are:
We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

How we work:
When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

As an equal opportunity employer, we welcome applications from individuals with disabilities.

We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities.

To all recruitment agencies:

Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated.