Commercial Packaging and Clinical Trial Supplies Manager

  • Salary: 77.96 CHF per hour
  • REF Number: v-99333
  • Consultant: Karen Kangley
  • Contact: 01246 457733
  • Date Published: 17.04.2024
  • Industry: Pharmaceutical
  • Location: Basel, Switzerland
  • Functional Expertise: Clinical Operations/Development

CK Group are recruiting for a Commercial Packaging and Clinical Trial Supply Manager to join a Swiss high-potential biopharmaceutical company, specialized in the discovery, development and commercialization of innovative small molecules, with the aim of transforming the horizon of therapeutic options. 

The position will be for a 12-month contract, located near at the clients office near Basel, the rate for this role will be 77.96 CHF per hour.

Job Responsibilities:

  • Project Manager responsible for packaging activities commercial and clinical
  • Work with CMC/ Product launch teams to align packaging operations
  • Support Pharmaceutical Serialization and anti-counterfeiting processes
  • Develop alongside DRA & Marketing the most suitable packaging format ensuring compliance to country specific requirements
  • Perform vendor selection for packaging partners
  • Manage packaging validation activities
  • Lead the packaging activities at packaging sites by defining the requirements
  • Establish packaging project plans and align with project team
  • Liaises with artwork provider for the timely completion of required work
  • Co-ordinate all internal & external documentation requirements for successful completion of activities
  • Work closely and continuously with cross functional team members and external service providers
  • Must have a willingness to share knowledge and to develop the team’s capabilities in commercial packaging
  • Willing to learn the new challenge of Clinical Trial supply management as part of the team


  • At least 5 years relevant experience in the Pharmaceutical industry
  • Working knowledge of commercial packaging activities, validation and artwork creation
  • Experience of working with and overseeing CMOs
  • Understanding of GMP packaging regulations and requirements
  • Serialization experience would be beneficial
  • Good project management skills, ability to handle multiple task and projects concurrently and a track record of delivering projects on time, to completion
  • Excellent team working skills within cross functional groups
  • Able to influence without authority
  • Fluent in English (Written and Spoken)


Entitlement to work in the EEA is essential. Please quote job reference 99333 in all correspondence.

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