Aseptic Process Specialist 16977
Veritaz AB
📍 Sverige
⏰ Heltid
📋 Vanlig anställning
🗓 Ansök senast 24 april 2026
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Skapa ansökan – från 49 kr Gratis att söka · Ingen registrering · 49 kr/mån för obegränsatOm jobbet
Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.
Assignment Description
We are looking for a Process Engineer
What You Will Work On
Perform validation and qualification of manufacturing processes
Handle deviations and support investigations in production
Conduct risk assessments related to processes and quality
Create and manage GMP-controlled documents
Issue and approve technical documentation
Ensure compliance with GMP standards and regulatory requirements
Collaborate with cross-functional teams in production and quality
What You Bring
Experience as a Process Engineer within pharmaceutical or similar regulated industry
Strong knowledge of sterile manufacturing and aseptic processes
Experience working in GMP-regulated environments
Experience with validation, qualification, and deviation handling
Ability to perform risk assessments and manage technical documentation
Strong analytical and problem-solving skills
Good communication and collaboration skills
Fluent in English
Assignment Description
We are looking for a Process Engineer
What You Will Work On
Perform validation and qualification of manufacturing processes
Handle deviations and support investigations in production
Conduct risk assessments related to processes and quality
Create and manage GMP-controlled documents
Issue and approve technical documentation
Ensure compliance with GMP standards and regulatory requirements
Collaborate with cross-functional teams in production and quality
What You Bring
Experience as a Process Engineer within pharmaceutical or similar regulated industry
Strong knowledge of sterile manufacturing and aseptic processes
Experience working in GMP-regulated environments
Experience with validation, qualification, and deviation handling
Ability to perform risk assessments and manage technical documentation
Strong analytical and problem-solving skills
Good communication and collaboration skills
Fluent in English