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NonStop Recruitment

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Job Details
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Process Expert in Drug Product - Matrix lead in Switzerland

Business Type: Biotechnology Company
Job Type: Biotechnology
Job Level: Experienced (non manager)
Position: Full Time
Salary: CHF80000 - CHF120000 per annum + 13% bonus
Location: France
Reference: 200411.1
Closing Date: 20/06/22
Job Details:

In order to support our continued growth, we are looking for experienced Process Experts with a relevant background in Drug Product / sterile manufacturing to join our talent community in Switzerland. Become part of this exciting opportunity and join our team by applying for the position as Process Experts Drug Product!


  • Competitive salary (90-120.000 CHF base)
  • Rewarding bonus structure (10-13% yearly bonus)
  • Canton privileges for families and children (generous family allowance, up to 550€ per child allowance)
  • Visa sponsorship (extended to family members)
  • Pension contributions (60%)
  • Relocation package
  • Settling allowance
  • Facilitation of opening a bank account
  • Additional employee-only benefits
  • Opportunity of unparalleled growth
  • Learn cross-functionally from other departments
  • International and cosmopolitan environment
  • Global experience

Key criteria for an interview invitation:

  • European nationality (mandatory)
  • Biotech experience of 3-5+ years
  • GMP experience preferable (or GMP like)
  • Experience in leading, implementing CAPA
  • Experience with Lyophilized products (preferable)
  • Experience with visual inspections (preferable)
  • Experience with SAP and MES
  • Proficient English

Key responsibilities:

  • Responsible for the planning, the execution and documentation of manufacturing campaigns for Drug Product in compliance to cGMPs, SOPs and applicable guidelines
  • Provide front line technical and procedural support, working with the manufacturing teams, plant engineers and QA operations
  • Lead process related investigations and critical deviations, assist in decision making on production issues and implement CAPAs as well as perform CAPA effectiveness checks
  • Responsible for the creation, modification, review and approval of batch records
  • Support technology transfer and product lifecycle

Key requirements:

  • Bachelor/ Master Degree / PhD, preferred area of study: Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy or equivalent scientific degree
  • Experience in the area of sterile drug product manufacturing
  • Fluent in English or in German, the knowledge of other languages is an asset.
  • Familiarity with GMP requirements, quality procedures and SOP execution
  • Good communication skills and interaction with a variety of interfaces within the organization and on the shopfloor
  • Proven IT knowledge, knowledge in SAP and MES is a plus

We offer a growth-oriented, dynamic environment, which offers challenging tasks across the entire network. If this opportunity resonates with you, make sure to apply.

If this role sounds like something you would be interested in, please send your CV by email to

If this role is not quite right for you but you would like to have a conversation about other roles, please search and connect with me, Orlando Nelson at NonStop, on LinkedIn.


Posted: 23/05/2022 | NPJ Ref: 306503
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