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Manufacturing Lead

TN Germany

Neumünster

Vor Ort

EUR 35.000 - 55.000

Vollzeit

Vor 9 Tagen

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Zusammenfassung

Ein etabliertes Unternehmen in der schnell wachsenden Cannabisbranche sucht einen Manufacturing Lead. In dieser Schlüsselrolle sind Sie verantwortlich für die sichere und effiziente Verarbeitung von Cannabis-Pflanzen gemäß GMP-Standards. Sie unterstützen die Planung und Organisation der Mitarbeiteraufgaben und stellen sicher, dass die Techniker die SOPs und EU-GMP-Anforderungen einhalten. Ihre Detailgenauigkeit und Ihr Engagement für hohe Qualitätsstandards werden entscheidend sein, um die Herstellung von hochwertigen Produkten zu gewährleisten. Wenn Sie eine Leidenschaft für die Verbesserung des Lebens anderer haben und in einer dynamischen Umgebung arbeiten möchten, ist dies die perfekte Gelegenheit für Sie.

Qualifikationen

  • Mindestens 1 Jahr Erfahrung in der Verarbeitung oder Produktion von medizinischen Produkten.
  • Erfahrung im Teammanagement und in einem GMP-Umfeld ist von Vorteil.

Aufgaben

  • Planung der Prozesse und Organisation der Mitarbeiteraufgaben.
  • Durchführung von Produktqualitätsprüfungen im Prozess.

Kenntnisse

Team Management
Attention to Detail
Good Documentation Practices
Task Focused

Ausbildung

High School diploma
Education as pharmaceutical technical assistant (PTA)

Tools

Microsoft Office Applications

Jobbeschreibung

Manufacturing Lead
Location: Neumünster - Germany

Tilray Brands is a leading global cannabis-lifestyle and consumer packaged goods company with operations in Canada, the United States, Europe, Australia, and Latin America that is changing people's lives for the better – one person at a time – by inspiring and empowering the worldwide community to live their very best life by providing them with products that meet the needs of their mind, body, and soul and invoke a sense of wellbeing. Tilray’s mission is to be the trusted partner for its patients and consumers by providing them with a cultivated experience and health and wellbeing through high-quality, differentiated brands and innovative products. A pioneer in cannabis research, cultivation, and distribution, Tilray’s unprecedented production platform supports over 20 brands in over 20 countries, including comprehensive cannabis offerings, hemp-based foods, and alcoholic beverages.

Overview: Looking to develop your career at the forefront of a rapidly expanding industry? Ready to apply your talents to make a positive difference in the lives of patients around the globe? The Manufacturing Lead is responsible for ensuring the completion of a safe and efficient GMP processing of cannabis plants to create various products for market. This role also assures that Technicians follow standard operating procedures (SOPs) and EU-GMP requirements to ensure the consistent and accurate processing of plants as medicinal products, meeting high quality standards.

Role and Responsibilities
  1. Support the planning processes, organize staff tasks and shift rotations.
  2. Manage the material stocks and transactions for the manufacturing processes according to the plan.
  3. Communicate and assist other manufacturing departments as needed.
  4. Support the maintenance of high-quality documentation in accordance with applicable regulatory guidance and site SOPs.
  5. Compile and analyze production batch records.
  6. Conduct product in-process quality checks.
  7. Support, if needed, the manufacturing and cleaning processes.
  8. Document work processes.
  9. Coordinate the work orders, physical inventory, and maintain the accuracy of the on-hand inventory count and transactions.
  10. Perform other duties as required related to manufacturing processes.
Qualifications and Education Requirements
  1. High School diploma (preferably) or education as pharmaceutical technical assistant (PTA) or Pharmakant.
  2. Minimum 1-year experience in processing or producing medicinal products or products for food executing repetitive tasks in a manufacturing or production setting.
  3. Experience in team management.
  4. Manufacturing experience in a GMP environment is an asset.
  5. Demonstrated ability to be “task focused” with meticulous attention to detail.
  6. Attention to detail and accuracy.
  7. Ability to perform and comply with the company’s Good Documentation Practices.
  8. Proven ability to effectively use Microsoft Office Applications.
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