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QA Cleaning and Process Validation Specialist

QA Cleaning and Process Validation Specialist

LocationVisp, Switzerland
Business SectorBiotechnology
Contact nameAliyana Darwesh
Contact email
Job ref22430
Publishedabout 2 months ago

QA Validation Engineer X2

Currently working with an innovative Biotech in need of support from X2 QA Validation Specialists focused on Cleaning and Process Validation for an urgent Remediation Project. This is an opportunity to work with a scale-up organization with a brand new state-of-the-art facility for a 4-month contract (extension expected).
 

Interview + offer will take place this week, so get in touch ASAP if interested.
 

Responsibilities:

  • Develop and implement cleaning plans according to GMP regulations and quality standards.
  • Collaborate on strategies for equipment and process cleaning.
  • Draft/review validation documents.
  • Conduct risk assessments and evaluate process impact.
  • Cleaning Validation protocol execution and summary report preparation
  • Identify and implement process improvements.
  • Evaluate changes and initiate change control processes.

 

Requirements:

  • 5+ years of GMP experience in the Biopharma industry
  • Significant background with drafting and reviewing validation documentation
  • Strong QA/Ops background
  • Collaborative personality with the ability to work efficiently and effectively in a fast-paced environment
  • Proficient in English; German is a plus!

 

Location: Valais, Switzerland                                                                                Start Date: ASAP                                                                                               On Site Presence: Hybrid
 

For more information, contact Aliyana Darwesh

+41 44 5514 407

a.darwesh@panda-int.com