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Process improvement specialist Breda SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • Medior/Senior
  • Engels (taal)

Aanbod

  • Vast contract
 

Vacature in het kort

Breda
Join a leading biotechnology company dedicated to advancing pharmaceuticals and making a global impact. In this role, you'll coordinate multi-site maintenance operations, ensuring cGMP compliance and driving process improvements. You'll manage procurement tasks, documentation, and performance metrics to boost efficiency. Collaborate with diverse teams, participate in audits, and help streamline operations. Enjoy the opportunity to contribute to innovative projects in a dynamic environment. Continue reading to see how you can contribute to our success story.
 

Over het bedrijf

SIRE Life Sciences
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The Company
This renowned biotechnology company specializes in developing the newest pharmaceuticals. With numerous facilities spanning across the globe, the company's primary focus is leveraging scientific research to create a positive impact on both humanity and the world. The Dutch facility plays a big part in the distribution part of the company.

Role Description
Supports multi-site Maintenance Operations projects by coordinating cross-functional activities, ensuring cGMP compliance, and driving process improvements. Manages procurement tasks, documentation, and performance metrics to enhance operational efficiency.

Responsibilities
-Coordinate and support multi-site, cross-departmental maintenance and engineering projects.
-Ensure compliance with cGMP, Amgen policies, and regulatory standards.
-Identify and implement process improvements with management approval.
-Support procurement activities including vendor evaluation, negotiation, and invoice verification.
-Draft, revise, and present documentation such as SOPs, training materials, and job plans.
-Collaborate with technicians, engineers, and other internal teams to support operations and achieve performance metrics.
-Compile, track, and report on departmental metrics and efficiencies.
-Participate in audits and regulatory inspections.
-Plan and manage Maximo work orders and act as a Work Administrator in the system.
-Facilitate and track progress on ongoing compliance and training programs.

Requirements
-Bachelor's degree OR Associate’s degree with 4 years of relevant experience 
-Strong attention to detail and ability to multitask in a fast-paced environment.
-Fluency in English (oral and written), with ability to proofread and follow detailed instructions.
-General understanding of customer needs and internal/external stakeholder relationships.
-Ability to work under general direction and escalate issues appropriately.

Other information
Apply to our vacancy below for more information. looking forward to hearing from you!
 

54859

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