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QA Manager

Job in Indiana Borough, Indiana County, Pennsylvania, 15705, USA
Listing for: Solvias
Full Time position
Listed on 2026-06-02
Job specializations:
  • IT/Tech
    Data Analyst, Data Security
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Description

  • We are looking for team players, who want to share their knowledge with our team and improve their personal capabilities.
  • Background in analytical chemistry / biochemistry / life science.
  • Experience in the analytical-pharmaceutical environment, preferably in QA.
  • Skills to solve problems and build a good relationship with various stakeholders.
  • Good interpersonal skills and team work spirit.
  • Ability to collaborate in a dynamic, cross-functional matrix environment.
  • Ability to lead projects between sites and work independently.
  • Broad knowledge and proven experience of the regulatory framework in the GMP environment (ICH, FDA, USP, Ph. Eur.).
  • Solid background in data integrity and computerized systems risk assessment and project support.
  • Experience as system administrator or deeper IT knowledge is an asset.
  • Fluency in English and German as a plus is required.
Responsibilities
  • Taking care of the quality management software as system administrator.
  • Support and train users.
  • Improve and update processes, including update of relevant SOPs and documents.
  • Harmonization of processes.
  • Leading projects.
  • Implementing additional modules / functionalities within the quality management software.
Qualifications
  • Background in analytical chemistry / biochemistry / life science.
  • Experience in the analytical-pharmaceutical environment, preferably in QA.
  • Skills to solve problems and build a good relationship with stakeholders.
  • Good interpersonal skills and team work spirit.
  • Ability to collaborate in a dynamic, cross-functional matrix environment.
  • Ability to lead projects between sites and work independently.
  • Broad knowledge and proven experience of the regulatory framework in the GMP environment (ICH, FDA, USP, Ph. Eur.).
  • Solid background in data integrity and computerized systems risk assessment and project support.
  • Experience as system administrator or deeper IT knowledge is an asset.
  • Fluency in English and German as a plus is required.
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