Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in securing 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 Senior Process Engineer or Validation Engineer to join our dynamic team

What You Will Work On:

• Engage as a Process Engineer or Validation Engineer within pharmaceutical manufacturing operations.
• Contribute to the development, optimization, and validation of manufacturing processes and equipment.
• Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards.
• Participate in the design, execution, and analysis of validation protocols and reports.
• Provide technical support and troubleshooting expertise to resolve manufacturing issues.
• Assist in the implementation of process improvements and efficiency enhancements.

What You Bring:

• Minimum of 3 years of university studies with a focus on disciplines such as mechanical engineering, biotechnology, or chemistry.
• Practical experience of at least 1 year in pharmaceutical manufacturing or an equivalent field.
• Hands-on experience of at least 1 year in the validation of equipment used in pharmaceutical manufacturing processes.
• Strong understanding of pharmaceutical manufacturing processes and regulatory requirements.
• Proficiency in conducting validation activities and interpreting validation data.
• Excellent problem-solving skills and attention to detail.
• Ability to work effectively in a cross-functional team environment.
• Strong communication and interpersonal skills.
• Adherence to high ethical standards and a commitment to quality and compliance.
• Fluent in Swedish and English.