Overview
Qa validation specialist Jobs in Valais, Switzerland at Oxford Global Resources
Are you looking for your next project in the pharmaceutical industry? Read on! About the Client Our client is an international leader in biotech and pharmaceutical production, with a strong footprint in Switzerland. Their facility in the Valais region operates at the forefront of bioprocessing
innovation
, combining
technical excellence
with an inspiring alpine setting. The site offers professionals a unique chance to develop their careers within a progressive and
collaborative
atmosphere.
Job Description
In this position, you will lead the creation and oversight of validation activities to support consistent and compliant biopharmaceutical manufacturing. You’ll play a vital role in process documentation, regulatory interaction, and interdepartmental
collaboration
. From design through continued verification, your work ensures robust quality standards. The role provides valuable exposure to both technical and strategic quality operations. Responsibilities Design comprehensive process validation plans that meet industry regulations.
Draft, review, and finalize validation protocols, reports, and assessments. Contribute to process characterization in partnership with R&D. Evaluate and authorize changes, deviations, and non-conformance events. Lead the development and maintenance of the continued process verification strategy. Provide input into Product Quality Reviews for life-cycle monitoring. Liaise with internal stakeholders to align validation and quality efforts. Engage with regulatory authorities when necessary.
Requirements Master’s degree in Chemistry, Biology, Biotechnology, Chemical Engineering, or related field. Proven background in
project management
within a GMP setting. Prior involvement in MSAT,
Quality Assurance
, or Operations. Exposure to biologics, particularly mammalian systems, is beneficial. Strong organizational skills with an ability to manage multiple priorities. Fluent in English;
German language knowledge is a plus.​​​​​​​ Benefits Contract for 7 months with Oxford Global Resources. Work at a pharmaceutical leader in a state of the art facility. Commuting allowance.
Title: Qa validation specialist
Company: Oxford Global Resources
Location: Valais, Switzerland
Category: Quality Assurance – QA/QC (Quality Engineering), Engineering (Quality Engineering, Process Engineer)
