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Job Details

Supply Chain Specialist (GMP – Drug Development and Manufacturing) – Lucerne/Schachen, Switzerland

Company: Clintec
Location:
Reference: WAG - 7812
Closing Date: 14 Feb 19
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Clintec currently has an exciting opportunity for an experienced Operational Planner/Supply Chain Specialist (GMP) to join our team in Switzerland, working fully dedicated to one of our clients – a top 5 global pharma company at their biological drug development and manufacturing site located near Lucerne, Switzerland.

Requirements:

This is an excellent role for a candidate to join our growing, global and award-winning company on a full time and permanent basis.

The individual will be responsible for coordinating packaging projects for the clinical supplies function. The successful candidate will provide support assigned projects from end-to-end including set up and coordination/monitoring throughout the assigned project to completion across the different work centres of the supply chain (label design/printing, packaging and QC).

Responsibilities:

  • Provide input and partner with other work centres to develop the packaging/labelling strategy for the individual clinical products
  • Monitor the adherence to project schedules and documents progress in respective databases
  • Assist the work centres (Global Project Management, Packaging, Label Operations, Quality disposition group) for issue resolution as needed
  • Collaborate with global master planning and project management (demand and supply project managers) to establish priorities across different projects
  • Negotiate timelines with contract manufacturers and requests/reviews quotes
  • Order multi-language booklet labels from third party suppliers
  • Generate Master Data (Material Master, Bill of Material, Recipe)
  • Generate project specific master documents (e.g. Batch Record)
  • Generate and release process/print orders for production
  • Work out proposals for continuous optimization of processes & procedures (SOPs) concerning clinical supply planning and packaging operations
  • Main POC for the Clinical Supplies Demand Manager and the contract manufacturer
  • Comply with GMP regulations
  • Develop, implement, and continuously improve processes and associated SOPs based on International Regulatory Standards, company Quality Guidelines and GMP regulations
  • Follow workflows and procedures according to current SOPs
  • Respect company policies concerning health and safety, finance and quality

Qualifications:

  • Educated to Bachelor degree level in Engineering, Life Sciences or another closely related discipline
  • 4+ years industry experience working within a pharmaceutical, biotechnology or medical device environment
  • Previous experience working within a GMP environment (familiar with requirements, quality procedures and SOPs)
  • Hands-on experience within any of the clinical supply areas: Planning, Scheduling, Coordination, Artwork and/or Label Translation  
  • Project Management Skills
  • Flexibility and ability to work as part of a team
  • Diligent and quality orientated
  • Proven ability to organise workload and manage multiple tasks at once to meet deadlines
  • Fluent in English and German languages
  • Ability to work site based in Schachen

Company Information:

Clintec is a dynamic, UK headquartered, privately owned, full service Contract Research Organisation with a presence in over 40 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assisting in their key product development efforts for over two decades. At Clintec we have experience in managing clinical trials in all major therapeutic areas including oncology, rare disease, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.

Clintec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. Clintec offers a competitive salary and rewards package.

Apply for this job: Supply Chain Specialist (GMP – Drug Development and Manufacturing) – Lucerne/Schachen, Switzerland

Contact Information:

Address:  Head Office
Clintec International Ltd,
133 Finnieston Street,
Glasgow
G3 8HB
Scotland
Tel:  +44 (0) 141 226 1120
Fax:  +44 (0) 141 248 8993
Website:  Visit Our Web Site

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