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LO
Lonza
last mo.

Senior QA Specialist, QA Operations(m/w/x)

Visp
Full-timeOn-siteSenior

Description

In this role, you will oversee quality assurance operations for a growth project, ensuring compliance and timely delivery by collaborating with various departments and making informed decisions on the manufacturing floor.

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Requirements

  • Academic degree in Life Sciences or related field
  • Significant experience in pharmaceutical Quality area
  • Work experience in Quality Assurance, Production or Engineering in pharmaceutical industries and cGMP regulated environment
  • Preferred QA experience in tech transfer
  • Excellent knowledge of computer systems and quality tools such as risk based approaches
  • Fluent English (written and verbal)

Education

Bachelor's degree

Work Experience

approx. 4 - 6 years

Tasks

  • Manage QA operations during commissioning and qualification
  • Assess and manage tasks impacting quality during GMP manufacturing
  • Plan future activities and coordinate with QC, Engineering, and Manufacturing
  • Support daily Quality Assurance activities per approved SOPs and policies
  • Review GMP records for compliance with cGMP procedures
  • Make real-time decisions on process events based on SOPs and policies
  • Participate in walkthroughs and audits/inspections

Tools & Technologies

TWSAP

Languages

EnglishBusiness Fluent

Benefits

Other Benefits

  • Lifestyle benefits
  • Relocation assistance

Family Support

  • Family benefits

Corporate Discounts

  • Leisure benefits
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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